PYRIDAZINOL COMPOUNDS AND DERIVATIVES, PREPARATION METHODS, HERBICIDAL COMPOSITIONS AND APPLICATIONS THEREOF

20220312770 · 2022-10-06

    Inventors

    Cpc classification

    International classification

    Abstract

    The invention belongs to the technical field of agricultural chemicals, and in particular relates to a pyridazinol compound represented by the Formula I, a derivative, preparation method, herbicidal composition and use thereof. The compound, derivative and herbicidal composition thereof have very high herbicidal activity and selectivity, and are safe for crops,

    ##STR00001##

    Claims

    1. A pyridazinol compound of Formula I or a derivative thereof: ##STR02157## wherein, X is halogenated alkyl, cyano, alkyl, alkoxy, halogenated alkoxy, R.sub.1R.sub.2N—(C═O)—, R.sub.1R.sub.2N—, hydroxy, or unsubstituted or substituted aryl; A is selected from the group consisting of alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, cycloalkylalkyl, aryl, heteroaryl, and aliphatic heterocyclyl, each of which is unsubstituted or substituted; wherein, when being substituted, each of said alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, or cycloalkylalkyl Is independently substituted with one or more substituents selected from the group consisting of halogen, cyano, nitro, azido, unsubstituted or substituted aryl, unsubstituted or substituted heteroaryl, —(CH.sub.2).sub.n—O—(CH.sub.2).sub.p—, —(CH.sub.2).sub.n—S—(CH.sub.2).sub.p, —(CH.sub.2).sub.n—NR.sub.3—(CH.sub.2).sub.p—, R—O—, R—O—(CH.sub.2).sub.p—O—, R—O—(CH.sub.2).sub.p—S—, R—S—, R—S—(CH.sub.2).sub.p—O—, R—S—(CH.sub.2).sub.p—S—, R—O—(CH.sub.2).sub.n—(C═O)—(CH.sub.2).sub.q—(O).sub.m—R—S—(CH.sub.2).sub.n—(C═S)—(CH.sub.2).sub.q—(S).sub.m—, R—O—(CH.sub.2).sub.n—(C═O)—(CH.sub.2).sub.q—(S).sub.m—, R—O—(CH.sub.2).sub.n—(C═S)—(CH.sub.2).sub.q—(O).sub.m—, R—S—(CH.sub.2).sub.n—(C═O)—(CH.sub.2).sub.q—(O).sub.m—, R—O—(CH.sub.2).sub.n—(C═S)—(CH.sub.2).sub.q—(S).sub.m—, R—S—(CH.sub.2).sub.n—(C═O)—(CH.sub.2).sub.q—(S).sub.m—, R—S—(CH.sub.2).sub.n—(C═S)—(CH.sub.2).sub.q—(O).sub.m—, R—(C═O)—, R—(C═S)—, R—(C═O)—(CH.sub.2).sub.n—O—, R—(C═S)—(CH.sub.2).sub.n—S—, R—(C═O)—(CH.sub.2).sub.n—S—, R—(C═S)—(CH.sub.2).sub.n—O—, R—SO—(CH.sub.2).sub.n—(O).sub.m—, R—SO—(CH.sub.2).sub.n—(S).sub.m—, R—SO—(CH.sub.2).sub.n—(NR.sub.3).sub.m—, R—SO.sub.2—(CH.sub.2).sub.n—(O).sub.m, R—SO.sub.2—(CH.sub.2).sub.n—(S).sub.m—, R—SO.sub.2—(CH.sub.2).sub.n—(NR.sub.3).sub.m—, R.sub.1R.sub.2N—, R.sub.1R.sub.2N—(CH.sub.2).sub.n—O—(CH.sub.2).sub.q—(O).sub.m—, R.sub.1R.sub.2N—(CH.sub.2).sub.n—O—(CH.sub.2).sub.q—(S).sub.m—, R.sub.1R.sub.2N—(CH.sub.2).sub.n—O—(CH.sub.2).sub.q—(NR.sub.3).sub.m—, R.sub.1R.sub.2N—(CH.sub.2).sub.n—(C═O)—(CH.sub.2).sub.q—(O).sub.m—, R.sub.1R.sub.2N—(CH.sub.2).sub.n—(C═O)—(CH.sub.2).sub.q—(S).sub.m—, R.sub.1R.sub.2N—(CH.sub.2).sub.n—(C═O)—(CH.sub.2).sub.q—(NR.sub.3).sub.m—, R.sub.1R.sub.2N—(CH.sub.2).sub.n—SO.sub.2—(CH.sub.2).sub.q—(O).sub.m—, R.sub.1R.sub.2N—(CH.sub.2).sub.n—SO.sub.2—(CH.sub.2).sub.q—(S).sub.m—, R.sub.1R.sub.2N—(CH.sub.2).sub.n—SO.sub.2—(CH.sub.2).sub.q—(NR.sub.3).sub.m—, R.sub.1R.sub.2P(O)—(O).sub.m—, R.sub.1R.sub.2R.sub.3SiO—, R.sub.1R.sub.2R.sub.3Si—(CH═CH).sub.m—, R.sub.1R.sub.2C═N—(O).sub.m—, and R.sub.1R.sub.2C═N—NH—; when being substituted, each of said aryl, heteroaryl, or aliphatic heterocyclyl is substituted with one or more substituents selected from the group consisting of halogen, cyano, nitro, azido, a halogen-containing or not containing group selected from alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, and cycloalkylalkyl, a group selected from aryl, arylalkyl, heteroaryl, heteroarylalkyl, aliphatic heterocyclyl, and aliphatic heterocyclylalkyl, which is unsubstituted or substituted, R—O—(CH.sub.2).sub.n—, R—O—(CH.sub.2).sub.p—O—(CH.sub.2).sub.q—, R—O—(CH.sub.2).sub.p—S—(CH.sub.2).sub.q—, R—S—(CH.sub.2).sub.n—, R—S—(CH.sub.2).sub.p—O—(CH.sub.2).sub.q—, R—S—(CH.sub.2).sub.p—S—(CH.sub.2).sub.q, R—O—(CH.sub.2).sub.n—(C═O)—(CH.sub.2).sub.q—(O).sub.m—, R—S—(CH.sub.2).sub.n—(C═S)—(CH.sub.2).sub.q—(S).sub.m—, R—O(CH.sub.2).sub.n—(C═O)—(CH.sub.2).sub.q—(S).sub.m—, R—O—(CH.sub.2).sub.n—(C═S)—(CH.sub.2).sub.q—(O).sub.m—, R—S—(CH.sub.2).sub.n—(C═O)—(CH.sub.2).sub.q—(O).sub.m—, R—O—(CH.sub.2).sub.n—(C═S)—(CH.sub.2).sub.q—(S).sub.m—, R—S—(CH.sub.2).sub.n—(C═O)—(CH.sub.2).sub.q—(S).sub.m—, R—S—(CH.sub.2).sub.n—(C═S)—(CH.sub.2).sub.q—(O).sub.m—, R—(C═O)—(CH.sub.2).sub.n—, R—(C═S)—(CH.sub.2).sub.n—, R—(C═O)—(CH.sub.2).sub.n—O—(CH.sub.2).sub.q—, R—(C═S)—(CH.sub.2).sub.n—S—(CH.sub.2).sub.q—, R—(C═O)—(CH.sub.2).sub.n—S—(CH.sub.2).sub.q—, R—(C═S)—(CH.sub.2).sub.n—O—(CH.sub.2).sub.q—, R—SO—(CH.sub.2).sub.n—(O).sub.m—, R—SO—(CH.sub.2).sub.n—(S).sub.m—, R—SO—(CH.sub.2).sub.n—(NR.sub.3).sub.m—, R—SO.sub.2—(CH.sub.2).sub.n—(O).sub.m—, R—SO.sub.2—(CH.sub.2).sub.n—(S).sub.m—, R—SO.sub.2—(CH.sub.2).sub.n—(NR.sub.3).sub.m—, R.sub.1R.sub.2N—(CH.sub.2).sub.n—, R.sub.1R.sub.2N—(CH.sub.2).sub.n—O—(CH.sub.2).sub.q—(O).sub.m—, R.sub.1R.sub.2N—(CH.sub.2).sub.n—O—(CH.sub.2).sub.q—(S).sub.m—, R.sub.1R.sub.2N—(CH.sub.2).sub.n—O—(CH.sub.2).sub.q—(NR.sub.3).sub.m—, R.sub.1R.sub.2N—(CH.sub.2).sub.n—(C═O)—(CH.sub.2).sub.q—(O).sub.m—, R.sub.1R.sub.2N—(CH.sub.2).sub.n—(C═O)—(CH.sub.2).sub.q—(S).sub.m—, R.sub.1R.sub.2N—(CH.sub.2).sub.n—(C═O)—(CH.sub.2).sub.q—(NR.sub.3).sub.m—, R.sub.1R.sub.2N—(CH.sub.2).sub.n—SO.sub.2—(CH.sub.2).sub.q—(O).sub.m, R.sub.1R.sub.2N—(CH.sub.2).sub.n—SO.sub.2—(CH.sub.2).sub.q—(S).sub.m—, R.sub.1R.sub.2N—(CH.sub.2).sub.n—SO.sub.2(CH.sub.2).sub.q—(NR.sub.3).sub.m—, R.sub.1R.sub.2PO.sub.3—(O).sub.m—(CH.sub.2).sub.q—, R.sub.1R.sub.2R.sub.3SiO—(CH.sub.2).sub.q—, R.sub.1R.sub.2R.sub.3Si—(CH═CH).sub.m—(CH.sub.2).sub.q—, R.sub.1R.sub.2C═N—(O).sub.m—(CH.sub.2).sub.n—, and R.sub.1R.sub.2C═N—NH—(CH.sub.2).sub.n—; m is 0 or 1, n and q are independently an integer from 0 to 8, p is an integer from 1 to 8; R is hydrogen, a halogen-containing or not containing group selected from alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, and cycloalkylalkyl, or a group selected from aryl, arylalkyl, heteroaryl, and heteroarylalkyl, which is unsubstituted or substituted; R.sub.1, R.sub.2, R.sub.3 are each independently hydrogen, nitro, hydroxy, amino, a halogen-containing or not containing group selected from alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, cycloalkylalkyl, alkoxy, alkenyloxy, alkynyloxy, cycloalkyloxy, alkoxyalkyl, alkoxycarbonyl, alkylsulfanylcarbonyl, alkylsulfonyl, alkylsulfonylalkyl, alkylcarbonyl, alkylcarbonylalkyl, alkylcarbonyloxy, alkylamino, alkylaminocarbonyl, alkoxyaminocarbonyl, alkoxycarbonylalkyl, alkylaminocarbonylalkyl, trialkylsilyl, and dialkylphosphonyl, or a group selected from aryl, arylalkyl, aryloxy, arylalkyloxy, aryloxyalkyl, arylcarbonyl, arylsulfonyl, heteroaryl, heteroarylalkyl, heteroaryloxy, heteroarylalkyloxy, heteroaryloxyalkyl, heteroarylcarbonyl, heteroarylsulfonyl, aliphatic heterocyclyl, aliphatic heterocyclylalkyl, aliphatic heterocyclyloxy, aliphatic heterocyclylalkoxy, aliphatic heterocyclyloxyalkyl, aliphatic heterocyclylcarbonyl, and aliphatic heterocyclylsulfonyl, which is unsubstituted or substituted; or R.sub.1R.sub.2N— forms a 5- to 6-membered heterocyclyl.

    2. The pyridazinol compound or a derivative thereof according to claim 1, wherein, X is halogenated C1˜C8 alkyl, cyano, C1˜C8 alkyl, C1˜C8 alkoxy, halogenated C1˜C8 alkoxy, R.sub.1R.sub.2N—(C═O)—, R.sub.1R.sub.2N—, hydroxy, or aryl, said aryl is unsubstituted or substituted with 1˜5 substituents independently selected from the group consisting of halogen, cyano, nitro, hydroxy, carboxyl, sulfhydryl, amino, and a halogen-containing or not containing group selected from C1˜C8 alkyl, C3˜C8 cycloalkyl, C3˜C8 cycloalkyl-C1˜C8 alkyl, C2˜C8 alkenyl, C2˜C8 alkynyl, C1˜C8 alkoxy, C1˜C8 alkylcarbonyl, C1˜C8 alkoxycarbonyl, C1˜C8 alkylsulfonyl, C1˜C8 alkylamino, and C1˜C8 alkylcarbonyloxy; A is selected from the group consisting of C1˜C8 alkyl, C2˜C8 alkenyl, C2˜C8 alkynyl, C3˜C8 cycloalkyl, C3˜C8 cycloalkenyl, C3˜C8 cycloalkyl-C1˜C8 alkyl, 5- to 14-membered aryl, 5- to 14-membered heteroaryl, and 5- to 14-membered aliphatic heterocyclyl, each of which is unsubstituted or substituted; wherein, when being substituted, said C1˜C8 alkyl, C2˜C8 alkenyl, C2˜C8 alkynyl, C3˜CS cycloalkyl, C3˜C6 cycloalkenyl, or C3˜C8 cycloalkyl-C1˜C8 alkyl is substituted with one or more substituents independently selected from the group consisting of halogen, cyano, nitro, azido, aryl, heteroaryl, said aryl or heteroaryl is unsubstituted or independently substituted with 15 groups selected from halogen, cyano, nitro, hydroxy, carboxyl, sulfhydryl, amino, and a halogen-containing or not containing group selected from C1˜C8 alkyl, C3˜C8 cycloalkyl, C3˜C8 cycloalkenyl, C3˜C8 cycloalkyl-C1˜C8 alkyl, C2˜C8 alkenyl, C2˜C8 alkynyl, C1˜C8 alkoxy, C1˜C8 alkylcarbonyl, C1˜C8 alkoxycarbonyl, C1˜C8 alkylsulfonyl, C1˜C8 alkylamino, and C1˜C8 alkylcarbonyloxy, —(CH.sub.2).sub.n—O—(CH.sub.2).sub.p—, —(CH.sub.2).sub.n—S—(CH.sub.2).sub.p—, —(CH.sub.2).sub.n—NR.sub.3—(CH.sub.2).sub.p—, R—O—, R—O—(CH.sub.2).sub.p—O—, R—O—(CH.sub.2).sub.p—S—, R—S—, R—S—(CH.sub.2).sub.p—O—, R—S—(CH.sub.2).sub.p—S—, R—O—(C═O)—(CH.sub.2).sub.q—(O).sub.m—, R—O—(CH.sub.2).sub.n—(C═O)—(O).sub.m—, R—O—(CH.sub.2).sub.n—(C═O)—, R—S—(C═S)—(CH.sub.2).sub.q—(S).sub.m—, R—S—(CH.sub.2).sub.n—(C═S)—(S).sub.m—, R—S—(CH.sub.2).sub.n—(C═S)—, R—O—(C═O)—(CH.sub.2).sub.q—(S).sub.m—, R—O—(CH.sub.2).sub.n—(C═O)—(S).sub.m—, R—O—(C═S)—(CH.sub.2).sub.q—(O).sub.m—, R—O—(CH.sub.2).sub.n—(C═S)—(O).sub.m—, R—O—(CH.sub.2).sub.n—(C═S)—, R—S—(C═O)—(CH.sub.2).sub.q—(O).sub.m—, R—S—(CH.sub.2).sub.n—(C═O)—(O).sub.m—, R—S—(CH.sub.2).sub.n—(C═O)—, R—O—(C═S)—(CH.sub.2).sub.q—(S).sub.m—, R—O—(CH.sub.2).sub.n—(C═S)—(S).sub.m—, R—S—(C═O)—(CH.sub.2).sub.q—(S).sub.m—, R—S—(CH.sub.2).sub.n—(C═O)—(S).sub.m—, R—S—(C═S)—(CH.sub.2).sub.q—(O).sub.m—, R—S—(CH.sub.2).sub.n—(C═S)—(O).sub.m—, R—(C═O)—, R—(C═S)—, R—(C═O)—O—, R—(C═S)—S—, R—(C═O)—S—, R—(C═S)—O—, R—SO—(O).sub.m—, R—SO—(S).sub.m—, R—SO—(NR.sub.3).sub.m—, R—SO.sub.2—(O).sub.m—, R—SO.sub.2—(S).sub.m—, R—SO.sub.2(NR.sub.3).sub.m, R.sub.1R.sub.2N—, R.sub.1R.sub.2N—O—(CH.sub.2).sub.q—(O).sub.m—, R.sub.1R.sub.2N—(CH.sub.2).sub.n—O—, R.sub.1R.sub.2N—O—(CH.sub.2).sub.q—(S).sub.m—, R.sub.1R.sub.2N—O—(CH.sub.2).sub.q—(NR.sub.3).sub.m—, R.sub.1R.sub.2N—(C═O)—(CH.sub.2).sub.q—(O).sub.m—, R.sub.1R.sub.2N—(CH.sub.2).sub.n—(C═O)—(O).sub.m—, R.sub.1R.sub.2N—(CH.sub.2).sub.n—(C═O)—, R.sub.1R.sub.2N—(C═O)—(CH.sub.2).sub.q—(S).sub.m—, R.sub.1R.sub.2N—(CH.sub.2).sub.n—(C═O)—(S).sub.m—, R.sub.1R.sub.2N—(C═O)—(CH.sub.2).sub.q—(NR.sub.3).sub.m—, R.sub.1R.sub.2N—(CH.sub.2).sub.n—(C═O)—(NR.sub.3).sub.m—, R.sub.1R.sub.2N—SO.sub.2—(CH.sub.2).sub.q—(O).sub.m—, R.sub.1R.sub.2N—(CH.sub.2).sub.n—SO.sub.2—(O).sub.m—, R.sub.1R.sub.2N—(CH.sub.2).sub.n—SO.sub.2—, R.sub.1R.sub.2N—SO.sub.2—(CH.sub.2).sub.q—(S).sub.m—, R.sub.1R.sub.2N—(CH.sub.2).sub.n—SO.sub.2—(S).sub.m—, R.sub.1R.sub.2N—SO.sub.2—(CH.sub.2).sub.q—(NR.sub.3).sub.m—, R.sub.1R.sub.2N—(CH.sub.2).sub.n—SO.sub.2—(NR.sub.3).sub.m—, R.sub.1R.sub.2P(O)—, R.sub.1R.sub.2R.sub.3SiO—, R.sub.1R.sub.2R.sub.3Si—(CH═CH).sub.m—, R.sub.1R.sub.2C═N—(O).sub.m—, and R.sub.1R.sub.2C═N—NH—; when being substituted, each of said 5- to 14-membered aryl, 5- to 14-membered heteroaryl or 5- to 14-membered aliphatic heterocyclyl is independently substituted with one or more substituents selected from the group consisting of halogen, cyano, nitro, azido, a halogen-containing or not containing group selected from C1˜C8 alkyl, C2˜C8 alkenyl, C2˜C8 alkynyl, C3˜C8 cycloalkyl, C3˜C8 cycloalkenyl, and C3˜CS cycloalkyl-C1˜C8 alkyl, aryl, aryl-C1˜C8 alkyl, heteroaryl, heteroaryl-C1˜C8 alkyl, aliphatic heterocyclyl, aliphatic heterocyclyl-C1˜C8 alkyl, each of said aryl, aryl-C1˜CS alkyl, heteroaryl, heteroaryl-C1˜C8 alkyl, aliphatic heterocyclyl, or aliphatic heterocyclyl-C1˜C8 alkyl is unsubstituted or substituted with 15 groups independently selected from halogen, cyano, nitro, hydroxy, carboxyl, sulfhydryl, amino, and a halogen-containing or not containing group selected from C1˜C8 alkyl, C3˜C8 cycloalkyl, C3˜C8 cycloalkenyl, C3˜C8 cycloalkyl-C1˜C8 alkyl, C2˜C8 alkenyl, C2˜C8 alkynyl, C1˜C8 alkoxy, C1˜C8 alkylcarbonyl, C1˜C8 alkoxycarbonyl, C1˜C8 alkylsulfonyl, C1˜C8 alkylamino, and C1˜C8 alkylcarbonyloxy, R—O—(CH.sub.2).sub.n—, R—O—(CH.sub.2).sub.p—O—(CH.sub.2).sub.q—, R—O—(CH.sub.2).sub.p—S—(CH.sub.2).sub.q—, R—S—(CH.sub.2).sub.n—, R—S—(CH.sub.2).sub.p—O—(CH.sub.2).sub.q—, R—S—(CH.sub.2).sub.p—S—(CH.sub.2).sub.q—, R—O—(CH.sub.2).sub.n—(C═O)—(CH.sub.2).sub.q—(O).sub.m—, R—S—(CH.sub.2).sub.n—(C═S)—(CH.sub.2).sub.q—, R—O—(CH.sub.2).sub.n—(C═S)—(CH.sub.2).sub.q—, R—S—(CH.sub.2).sub.n—(C═O)—(CH.sub.2).sub.q—, R—S—(C═S)—(CH.sub.2).sub.q—(S).sub.m—, R—O—(CH.sub.2).sub.n—(C═O)—(CH.sub.2).sub.q—(S).sub.m—, R—O—(C═S)—(CH.sub.2).sub.q—(O).sub.m—, R—S—(C═O)—(CH.sub.2).sub.q—(O).sub.m—, R—O—(C═S)—(CH.sub.2).sub.q—(S).sub.m—, R—S—(C═O)—(CH.sub.2).sub.q—(S).sub.m—, R—S—(C═S)—(CH.sub.2).sub.q—(O).sub.m—, R—S—(CH.sub.2).sub.n—(C═S)—(S).sub.m—, R—O—(CH.sub.2).sub.n—(C═S)—(O).sub.m—, R—S—(CH.sub.2).sub.n—(C═O)—(O).sub.m—, R—O—(CH.sub.2).sub.n—(C═S)—(S).sub.m—, R—S—(CH.sub.2).sub.n—(C═O)—(S).sub.m—, R—S—(CH.sub.2).sub.n—(C═S)—(O).sub.m—, R—(C═O)—(CH.sub.2).sub.n—, R—(C═S)—, R—(C═O)—(CH.sub.2).sub.n—O—(CH.sub.2).sub.q—, R—(C═S)—(CH.sub.2).sub.n—S—, R—(C═O)—(CH.sub.2).sub.n—S—, R—(C═S)—(CH.sub.2).sub.n—O—, R—(C═S)—S—(CH.sub.2).sub.q—, R—(C═O)—S—(CH.sub.2).sub.q—, R—(C═S)—O—(CH.sub.2).sub.q—, R—SO—(O).sub.m—, R—SO—(S).sub.m—, R—SO(NR.sub.3).sub.m, R—SO.sub.2—(CH.sub.2).sub.n—(O).sub.m, R—SO.sub.2—(S).sub.m—, R—SO.sub.2(CH.sub.2).sub.n—(NR.sub.3).sub.m—, R—SO—(CH.sub.2).sub.n—, R.sub.1R.sub.2N—(CH.sub.2).sub.n—, R.sub.1R.sub.2N—(CH.sub.2).sub.n—O—(CH.sub.2).sub.q—, R.sub.1R.sub.2N—(C═O)—(CH.sub.2).sub.q—(O).sub.m—, R.sub.1R.sub.2N—(CH.sub.2).sub.n—(C═O)—(CH.sub.2).sub.q—, R.sub.1R.sub.2N—(CH.sub.2).sub.n—(C═O)—(O).sub.m—, R.sub.1R.sub.2N—(CH.sub.2).sub.n—(C═O)—(S).sub.m—, R.sub.1R.sub.2N—(CH.sub.2).sub.n—(C═O)—(NR.sub.3).sub.m—, R.sub.1R.sub.2N—(CH.sub.2).sub.n—SO.sub.2—(CH.sub.2).sub.q—(O).sub.m—, R.sub.1R.sub.2N—(CH.sub.2).sub.n—SO.sub.2—(S).sub.m—, R.sub.1R.sub.2N—(CH.sub.2).sub.n—SO.sub.2—(NR.sub.3).sub.m—, R.sub.1R.sub.2N—(C═O)—(CH.sub.2).sub.n—(O).sub.m—, R.sub.1R.sub.2N—(C═O)—(CH.sub.2).sub.n—(S).sub.m—, R.sub.1R.sub.2N—(C═O)—(CH.sub.2).sub.n—(NR.sub.3).sub.m—, R.sub.1R.sub.2N—SO.sub.2—(CH.sub.2).sub.q—(S).sub.m—, R.sub.1R.sub.2N—SO.sub.2—(CH.sub.2).sub.q—(NR.sub.3).sub.m—, R.sub.1R.sub.2N—(CH.sub.2).sub.n—O—, R.sub.1R.sub.2N—O—(CH.sub.2).sub.q—, R.sub.1R.sub.2P(O)—(O).sub.m—, R.sub.1R.sub.2R.sub.3SiO—, R.sub.1R.sub.2R.sub.3Si—(CH═CH).sub.m, R.sub.1R.sub.2C═N—(O).sub.m—, and R.sub.1R.sub.2C═N—NH—; m is 0 or 1, n and q are independently an integer from 0 to 6, p is an integer from 1 to 6; R is hydrogen, a halogen-containing or not containing group selected from C1˜C8 alkyl, C2˜C8 alkenyl, C2˜C8 alkynyl, C3˜C8 cycloalkyl, C3˜C8 cycloalkenyl, and C3˜C8 cycloalkyl-C1˜C8 alkyl, aryl, aryl-C1˜C8 alkyl, heteroaryl, or heteroaryl-C1˜C8 alkyl, each of said aryl, aryl-C1˜C8 alkyl, heteroaryl, or heteroaryl-C1˜C8 alkyl is unsubstituted or substituted with 1˜5 groups substituents independently selected from halogen, cyano, nitro, hydroxy, carboxyl, sulfhydryl, amino, and a halogen-containing or not containing group selected from C1˜C8 alkyl, C3˜C8 cycloalkyl, C3˜C8 cycloalkenyl, C3˜C8 cycloalkyl-C1˜C8 alkyl, C2˜C6 alkenyl, C2˜C8 alkynyl, C1˜C8 alkoxy, C1˜C8 alkylcarbonyl, C1˜C8 alkoxycarbonyl, C1˜C8 alkylsulfonyl, C1˜C8 alkylamino, and C1˜C8 alkylcarbonyloxy; R.sub.1, R.sub.2, R.sub.3 are each independently hydrogen, nitro, hydroxy, amino, a halogen-containing or not containing group selected from C1˜CS alkyl, C2˜C8 alkenyl, C2˜C8 alkynyl, C3˜C8 cycloalkyl, C3˜C8 cycloalkenyl, C3˜C8 cycloalkyl-C1˜C8 alkyl, C1˜C8 alkoxy, C2˜C8 alkenyloxy, C2˜C8 alkynyloxy, C3˜C8 cycloalkyloxy, C1˜C8 alkoxy-C1˜C8 alkyl, C1˜C8 alkoxycarbonyl, C1˜C8 alkylcarbonyl-C1˜C8 alkyl, C1˜C8 alkylsulfanylcarbonyl, C1˜C8 alkylsulfonyl, C1˜C8 alkylsulfonyl-C1˜C8 alkyl, C1˜C8 alkylcarbonyl, C1˜C8 alkylcarbonyloxy, C1˜C8 alkylamino, C1˜C8 alkylaminocarbonyl, C1˜C8 alkoxyaminocarbonyl, C1˜C8 alkoxycarbonyl-C1˜C8 alkyl, C1˜C8 alkylaminocarbonyl-C1˜C8 alkyl, triC1˜CS alkylsilyl, and diC1˜C8 alkylphosphonyl, aryl, aryl-C1˜CS alkyl, aryloxy, aryl-C1˜C8 alkyloxy, aryloxy-C1˜C8 alkyl, arylcarbonyl, arylsulfonyl, heteroaryl, heteroaryl-C1˜C8 alkyl, heteroaryloxy, heteroaryl-C1˜C8 alkyloxy, heteroaryloxy-C1˜C8 alkyl, heteroarylcarbonyl, heteroarylsulfonyl, aliphatic heterocyclyl, aliphatic heterocyclyl-C1˜C8 alkyl, aliphatic heterocyclyloxy, aliphatic heterocyclyl-C1˜C8 alkyloxy, aliphatic heterocyclyloxy-C1˜C8 alkyl, aliphatic heterocyclylcarbonyl, or aliphatic heterocyclylsulfonyl, each of said aryl, aryl-C1˜C8 alkyl, aryloxy, aryl-C1˜C8 alkyloxy, aryloxy-C1˜C8 alkyl, arylcarbonyl, arylsulfonyl, heteroaryl, heteroaryl-C1˜C8 alkyl, heteroaryloxy, heteroaryl-C1˜C8 alkyloxy, heteroaryloxy-C1˜C8 alkyl, heteroarylcarbonyl, heteroarylsulfonyl, aliphatic heterocyclyl, aliphatic heterocyclyl-C1˜C8 alkyl, aliphatic heterocyclyloxy, aliphatic heterocyclyl-C1˜C8 alkyloxy, aliphatic heterocyclyloxy-C1˜C8 alkyl, aliphatic heterocyclylcarbonyl, or aliphatic heterocyclylsulfonyl is unsubstituted or substituted with 1˜5 groups independently selected from halogen, cyano, nitro, hydroxy, carboxyl, sulfhydryl, amino, and a halogen-containing or not containing group selected from C1˜C8 alkyl, C3˜C8 cycloalkyl, C3˜C8 cycloalkenyl, C3˜C8 cycloalkyl-C1˜C8 alkyl, C2˜C8 alkenyl, C2˜C8 alkynyl, C1˜C8 alkoxy, C1˜C8 alkylcarbonyl, C1˜C8 alkoxycarbonyl, C1˜C8 alkylsulfonyl, C1˜CS alkylamino, and C1˜C8 alkylcarbonyloxy; or R.sub.1R.sub.2N— forms a 5- to 6-membered heterocyclyl; wherein the derivative is an agriculturally acceptable salt or a compound derivatized from the 4-hydroxy of the pyridazlne ring of the Formula I.

    3. The pyridazinol compound or a derivative thereof according to claim 1, wherein, X is halogenated C1˜C6 alkyl; A is selected from the group consisting of C1˜C6 alkyl, C2˜C6 alkenyl, C2˜C6 alkynyl, C3˜C6 cycloalkyl, C3˜C6 cycloalkenyl, C3˜C6 cycloalkyl-C1˜C6 alkyl, 5- to 14-membered aryl, 5- to 14-membered heteroaryl, and 5- to 14-membered aliphatic heterocyclyl, each of which is unsubstituted or substituted; wherein, when being substituted, each of said C1˜C6 alkyl, C2˜C6 alkenyl, C2˜C6 alkynyl, C3˜CS cycloalkyl, C3˜C6 cycloalkenyl, or C3˜C6 cycloalkyl-C1˜C6 alkyl is substituted with one or more substituents independently selected from the group consisting of halogen, cyano, nitro, azido, aryl, heteroaryl, said aryl or heteroaryl is unsubstituted or substituted with 1˜3 groups independently selected from halogen, cyano, nitro, hydroxy, carboxyl, sulfhydryl, amino, and a halogen-containing or not containing group selected from C1˜C6 alkyl, C3˜C6 cycloalkyl, C3˜C6 cycloalkenyl, C3˜C6 cycloalkyl-C1˜C6 alkyl, C2˜C6 alkenyl, C2˜C6 alkynyl, C1˜C6 alkoxy, C1˜CS alkylcarbonyl, C1˜C6 alkoxycarbonyl, C1˜C6 alkylsulfonyl, C1˜C6 alkylamino, and C1˜C6 alkylcarbonyloxy, —(CH.sub.2).sub.n—O—, —(CH.sub.2).sub.n—S—, —(CH.sub.2).sub.n—NR.sub.3—, R—O—, R—O—(CH.sub.2).sub.p—O—, R—O—(CH.sub.2).sub.p—S—, R—S—, R—S—(CH.sub.2).sub.p—O—, R—S—(CH.sub.2).sub.p—S—, R—O—(CH.sub.2).sub.n—(C═O)—, R—S—(C═S)—, R—O—(C═S)—, R—S—(C═O)—, R—(C═O)—, R—(C═S)—, R—(C═O)—O—, R—(C═S)—S—, R—(C═O)—S—, R—(C═S)—O—, R—SO—, R—SO.sub.2—, R.sub.1R.sub.2N—, R.sub.1R.sub.2N—O—, R.sub.1R.sub.2N—(C═O), R.sub.1R.sub.2N—SO.sub.2—, R.sub.1R.sub.2P(O)—, R.sub.1R.sub.2R.sub.3SiO—, R.sub.1R.sub.2R.sub.3Si—(CH═CH)—, R.sub.1R.sub.2R.sub.3Si—, R.sub.1R.sub.2C═N—(O)—, R.sub.1R.sub.2C═N—, and R.sub.1R.sub.2C═N—NH—; when being substituted, each of said 5- to 14-membered aryl, 5- to 14-membered heteroaryl or 5- to 14-membered aliphatic heterocyclyl is substituted with one or more substituents independently selected from the group consisting of halogen, cyano, nitro, azido, a halogen-containing or not containing group selected from C1˜C6 alkyl, C2˜C6 alkenyl, C2˜C6 alkynyl, C3˜C6 cycloalkyl, C3˜C6 cycloalkenyl, and C3˜C6 cycloalkyl-C1˜C6 alkyl, aryl, aryl-C1˜C6 alkyl, heteroaryl, heteroaryl-C1˜C6 alkyl, aliphatic heterocyclyl, aliphatic heterocyclyl-C1˜C6 alkyl, each of said aryl, aryl-C1˜C6 alkyl, heteroaryl, heteroaryl-C1˜C6 alkyl, aliphatic heterocyclyl, or aliphatic heterocyclyl-C1˜C6 alkyl is unsubstituted or substituted with 1˜5 groups independently selected from halogen, cyano, nitro, hydroxy, carboxyl, sulfhydryl, amino, and a halogen-containing or not containing group selected from C1˜C6 alkyl, C3˜C6 cycloalkyl, C3˜C6 cycloalkenyl, C3˜C6 cycloalkyl-C1˜C6 alkyl, C2˜C6 alkenyl, C2˜C8 alkynyl, C1˜C8 alkoxy, C1˜C6 alkylcarbonyl, C1˜C6 alkoxycarbonyl, C1˜C6 alkylsulfonyl, C1˜C6 alkylamino, and C1˜C6 alkylcarbonyloxy, R—O—(CH.sub.2).sub.n—, R—O—(CH.sub.2).sub.pO—, R—O—(CH.sub.2).sub.p—S—, R—S—(CH.sub.2).sub.n—, R—O—(CH.sub.2).sub.n—(C═O)—(CH.sub.2).sub.q—(O).sub.m—, R—O—(CH.sub.2).sub.n—(C═O)—(CH.sub.2).sub.q—(S).sub.m—, R—S—(CH.sub.2).sub.p—O—, R—S—(CH.sub.2).sub.p—S—, R—S—(C═S)—(S).sub.m—, R—O—(C═S)—(O).sub.m—, R—S—(CH.sub.2).sub.n—(C═O)—(O).sub.m—, R—O—(C═S)—(S).sub.m—, R—S—(C═O)—(S).sub.m—, R—S—(C═S)—(O).sub.m—, R—S—(C═S)—(CH.sub.2).sub.q—, R—O—(C═S)—(CH.sub.2).sub.q—, R—S—(C═O)—(CH.sub.2).sub.q—, R—S—(CH.sub.2).sub.n—(C═S)—, R—O—(CH.sub.2).sub.n—(C═S)—, R—S—(CH.sub.2).sub.n—(C═O)—, R—(C═O)—(CH.sub.2).sub.n—, R—(C═S)—, R—(C═O)—(CH.sub.2).sub.n—O—(CH.sub.2).sub.q—, R—(C═S)—S—, R—(C═O)—S—, R—(C═S)—O—, R—SO—(CH.sub.2).sub.n—, R—SO.sub.2—(CH.sub.2).sub.n—(O).sub.m—, R—SO.sub.2—(CH.sub.2).sub.n—(NR.sub.3).sub.m—, R.sub.1R.sub.2N—(CH.sub.2).sub.n—, R.sub.1R.sub.2N—O—, R.sub.1R.sub.2N—(C═O)—(CH.sub.2).sub.q—(O).sub.m—, R.sub.1R.sub.2N—(C═O)—(S).sub.m—, R.sub.1R.sub.2N—(C═O)—(NR.sub.3).sub.m—, R.sub.1R.sub.2N—(CH.sub.2).sub.n—SO.sub.2—(CH.sub.2).sub.q—(O).sub.m—, R.sub.1R.sub.2N—(CH.sub.2).sub.p—(C═O)—, R.sub.1R.sub.2N—(CH.sub.2).sub.p—O—, R.sub.1R.sub.2N—O—(CH.sub.2).sub.p, R.sub.1R.sub.2P(O)—, R.sub.1R.sub.2R.sub.3SiO—, R.sub.1R.sub.2R.sub.3Si—, R.sub.1R.sub.2R.sub.3Si—CH═CH, R.sub.1R.sub.2C═N—, R.sub.1R.sub.2C═N—O—, and R.sub.1R.sub.2C═N—NH—; m is 0 or 1, n and q are each independently an integer from 0 to 4, p is an integer from 1 to 4; R is hydrogen, a halogen-containing or not containing group selected from C1˜C6 alkyl, C2˜C6 alkenyl, C2˜C6 alkynyl, C3˜C6 cycloalkyl, C3˜C8 cycloalkenyl, and C3˜C6 cycloalkyl-C1˜C6 alkyl, aryl, aryl-C1˜C6 alkyl, heteroaryl, or heteroaryl-C1˜C6 alkyl, each of said aryl, aryl-C.sub.1˜C6 alkyl, heteroaryl, or heteroaryl-C1˜C6 alkyl is unsubstituted or substituted with 1˜3 groups independently selected from halogen, cyano, nitro, hydroxy, carboxyl, sulfhydryl, amino, and a halogen-containing or not containing group selected from C1˜C6 alkyl, C3˜C6 cycloalkyl, C3˜C6 cycloalkenyl, C3˜C6 cycloalkyl-C1˜C6 alkyl, C2˜C6 alkenyl, C2˜C6 alkynyl, C1˜C6 alkoxy, C1˜C6 alkylcarbonyl, C1˜C6 alkoxycarbonyl, C1˜C6 alkylsulfonyl, C1˜C8 alkylamino, and C1˜C6 alkylcarbonyloxy; R.sub.1, R.sub.2, R.sub.3 are each independently is hydrogen, nitro, hydroxy, amino, a halogen-containing or not containing group selected from C1˜C6 alkyl, C2˜C6 alkenyl, C2˜C8 alkynyl, C3˜C6 cycloalkyl, C3˜C6 cycloalkenyl, C3˜C6 cycloalkyl-C1˜C6 alkyl, C1˜C6 alkoxy, C2˜C6 alkenyloxy, C2˜C6 alkynyloxy, C3˜C6 cycloalkyloxy, C1˜C6 alkoxy-C1˜C6 alkyl, C1˜C6 alkoxycarbonyl, C1˜C6 alkylsulfanylcarbonyl, C1˜C6 alkylsulfonyl, C1˜C8 alkylsulfonyl-C1˜C6 alkyl, C1˜C6 alkylcarbonyl, C1˜C6 alkylcarbonyl-C1˜C8 alkyl, C1˜C6 alkylcarbonyloxy, C1˜C8 alkylamino, C1˜C6 alkylaminocarbonyl, C1˜C6 alkoxyaminocarbonyl, C1˜C6 alkoxycarbonyl-C1˜C8 alkyl, C1˜C6 alkylaminocarbonyl-C1˜C6 alkyl, triC1˜C6 alkylsilyl, and diC1˜C6 alkylphosphonyl, aryl, aryl-C1˜C6 alkyl, aryloxy, aryl-C1˜C6 alkyloxy, aryloxy-C1˜C6 alkyl, arylcarbonyl, arylsulfonyl, heteroaryl, heteroaryl-C1˜C8 alkyl, heteroaryloxy, heteroaryl-C1˜C6 alkyloxy, heteroaryloxy-C1˜C6 alkyl, heteroarylcarbonyl, heteroarylsulfonyl, aliphatic heterocyclyl, aliphatic heterocyclyl-C1˜C6 alkyl, aliphatic heterocyclyloxy, aliphatic heterocyclyl-C1˜C6 alkyloxy, aliphatic heterocyclyloxy-C1˜C6 alkyl, aliphatic heterocyclylcarbonyl, or aliphatic heterocyclylsulfonyl, each of said aryl, aryl-C1˜C6 alkyl, aryloxy, aryl-C1˜C6 alkyloxy, aryloxy-C1˜C6 alkyl, arylcarbonyl, arylsulfonyl, heteroaryl, heteroaryl-C1˜C6 alkyl, heteroaryloxy, heteroaryl-C1˜C6 alkyloxy, heteroaryloxy-C1˜C8 alkyl, heteroarylcarbonyl, heteroarylsulfonyl, aliphatic heterocyclyl, aliphatic heterocyclyl-C1˜C6 alkyl, aliphatic heterocyclyloxy, aliphatic heterocyclyl-C1˜C8 alkyloxy, aliphatic heterocyclyloxy-C1˜C6 alkyl, aliphatic heterocyclylcarbonyl, or aliphatic heterocyclylsulfonyl is unsubstituted or substituted with 1˜3 groups independently selected from halogen, cyano, nitro, hydroxy, carboxyl, sulfhydryl, amino, and a halogen-containing or not containing group selected from C1˜CS alkyl, C3˜C6 cycloalkyl, C3˜C6 cycloalkenyl, C3˜C6 cycloalkyl-C1˜C6 alkyl, C2˜C6 alkenyl, C2˜C6 alkynyl, C1˜C6 alkoxy, C1˜C6 alkylcarbonyl, C1˜C6 alkoxycarbonyl, C1˜C6 alkylsulfonyl, C1˜C6 alkylamino, and C1˜C6 alkylcarbonyloxy; or R.sub.1R.sub.2N— is ##STR02158## the aryl is selected from ##STR02159## the heteroaryl is selected from ##STR02160## ##STR02161## ##STR02162## R′ is hydrogen, nitro, hydroxy, amino, a fluoro-, chloro-, or bromo-containing or not containing group selected from C1˜C8 alkyl, C2˜C6 alkenyl, C2˜C6 alkynyl, C3˜C8 cycloalkyl, C3˜C6 cycloalkenyl, C3˜C8 cycloalkyl-C1˜C8 alkyl, C1˜C6 alkoxy, C2˜C8 alkenyloxy, C2˜C6 alkynyloxy, C3˜C8 cycloalkyloxy, C1˜C6 alkoxy-C1˜C8 alkyl, C1˜C6 alkoxycarbonyl, C1˜C6 alkylsulfanylcarbonyl, C1˜C6 alkylsulfonyl, C1˜C6 alkylsulfonyl-C1˜C6 alkyl, C1˜C6 alkylcarbonyl, C1˜C6 alkylcarbonyl-C1˜C6 alkyl, C1˜C6 alkylcarbonyloxy, C1˜C6 alkylamino, C1˜C6 alkylaminocarbonyl, C1˜C6 alkoxyaminocarbonyl, C1˜C8 alkoxycarbonyl-C1˜C6 alkyl, C1˜C8 alkylaminocarbonyl-C1˜C6 alkyl, triC1˜C6 alkylsilyl, and diC1˜C6 alkylphosphonyl, aryl, aryl-C1˜C6 alkyl, aryloxy, aryl-C1˜C6 alkyloxy, aryloxy-C1˜C6 alkyl, arylcarbonyl, arylsulfonyl, heteroaryl, heteroaryl-C1˜C6 alkyl, heteroaryloxy, heteroaryl-C1˜C6 alkyloxy, heteroaryloxy-C1˜C8 alkyl, heteroarylcarbonyl, heteroarylsulfonyl, aliphatic heterocyclyl, aliphatic heterocyclyl-C1˜C6 alkyl, aliphatic heterocyclyloxy, aliphatic heterocyclyl-C1˜C6 alkyloxy, aliphatic heterocyclyloxy-C1˜C6 alkyl, aliphatic heterocyclylcarbonyl, or aliphatic heterocyclylsulfonyl, each of said aryl, aryl-C1˜C6 alkyl, aryloxy, aryl-C1˜C8 alkyloxy, aryloxy-C1˜C6 alkyl, arylcarbonyl, arylsulfonyl, heteroaryl, heteroaryl-C1˜C6 alkyl, heteroaryloxy, heteroaryl-C1˜CS alkyloxy, heteroaryloxy-C1˜C6 alkyl, heteroarylcarbonyl, heteroarylsulfonyl, aliphatic heterocyclyl, aliphatic heterocyclyl-C1˜C6 alkyl, aliphatic heterocyclyloxy, aliphatic heterocyclyl-C1˜C6 alkyloxy, aliphatic heterocyclyloxy-C1˜C6 alkyl, aliphatic heterocyclylcarbonyl, or aliphatic heterocyclylsulfonyl is unsubstituted or substituted with 1-3 groups independently selected from fluorine, chlorine, bromine, cyano, nitro, hydroxy, carboxyl, sulfhydryl, amino, and a fluoro-, chloro-, bromo-containing or not containing group selected from C1˜C6 alkyl, C3˜C8 cycloalkyl, C3˜C6 cycloalkenyl, C3˜C6 cycloalkyl-C1˜C6 alkyl, C2˜C6 alkenyl, C2˜C6 alkynyl, C1˜C6 alkoxy, C1˜C6 alkylcarbonyl, C1˜C6 alkoxycarbonyl, C1˜C6 alkylsulfonyl, C1˜C6 alkylamino, and C1˜C6 alkylcarbonyloxy; the aliphatic heterocyclyl is selected from ##STR02163## wherein the derivative is an agriculturally acceptable salt or a compound derivatized from 4-hydroxy of the pyridazine ring of the Formula I, including an ester, an oxime, a hydroxylamine and an ether thereof.

    4. The pyridazinol compound or a derivative thereof according to claim 1, wherein, X is halogenated C1˜C6 alkyl; A is selected from the group consisting of C1˜C6 alkyl, C2˜C6 alkenyl, C3˜C6 cycloalkyl, C3˜C6 cycloalkenyl, 5- to 14-membered aryl, 5- to 14-membered heteroaryl, and 5- to 14-membered aliphatic heterocyclyl, each of which is unsubstituted or substituted; wherein, when being substituted, said C1˜C6 alkyl, C2˜C6 alkenyl, C3˜C6 cycloalkyl, or C3˜C6 cycloalkenyl is substituted with one or more substituents independently selected from R—O—(CH.sub.2).sub.n—(C═O)— and R.sub.1R.sub.2R.sub.3SiO—; when being substituted, said 5- to 14-membered aryl, 5- to 14-membered heteroaryl or 5- to 14-membered aliphatic heterocyclyl is substituted with one or more substituents independently selected from the group consisting of halogen, cyano, nitro, azido, a halogen-containing or not containing group selected from C1˜C6 alkyl, C2˜C6 alkenyl, C2˜C6 alkynyl, C3˜C8 cycloalkyl, and C3˜C6 cycloalkyl-C1˜C6 alkyl, aryl, aryl-C1˜C6 alkyl, heteroaryl, heteroaryl-C1˜C6 alkyl, aliphatic heterocyclyl, aliphatic heterocyclyl-C1˜C6 alkyl, each of said aryl, aryl-C1˜C8 alkyl, heteroaryl, heteroaryl-C1˜C6 alkyl, aliphatic heterocyclyl, or aliphatic heterocyclyl-C1˜C6 alkyl is unsubstituted or substituted with 1-5 groups independently selected from halogen, cyano, nitro, hydroxy, carboxyl, sulfhydryl, amino, and a halogen-containing or not containing group selected from C1˜C6 alkyl, C3˜C6 cycloalkyl, C3˜C6 cycloalkyl-C1˜C6 alkyl, C2˜C6 alkenyl, C2˜C6 alkynyl, C1˜C8 alkoxy, C1˜C6 alkylcarbonyl, C1˜C6 alkoxycarbonyl, C1˜C6 alkylsulfonyl, C1˜C6 alkylamino, and C1˜C6 alkylcarbonyloxy, R—O—(CH.sub.2).sub.n—, R—O—(CH.sub.2).sub.p—O—, R—S—(CH.sub.2).sub.n—, R—O—(CH.sub.2).sub.n—(C═O)—(CH.sub.2).sub.q—(O).sub.m—, R—O—(CH.sub.2).sub.n—(C═O)—(CH.sub.2).sub.q—(S).sub.m—, R—S—(CH.sub.2).sub.n—(C═O)—, R—(C═O)—(CH.sub.2).sub.n—, R—(C═O)—(CH.sub.2).sub.n—O—(CH.sub.2).sub.q—, R—SO—(CH.sub.2).sub.n—, R—SO.sub.2—(CH.sub.2).sub.n—(O).sub.m—, R—SO.sub.2—(CH.sub.2).sub.n—(NR.sub.3).sub.m—, R.sub.1R.sub.2N—(C═O)—(CH.sub.2).sub.q—(O).sub.m—, R.sub.1R.sub.2N—(C═O)—(NR.sub.3).sub.m—, R.sub.1R.sub.2N—(CH.sub.2).sub.n—, R.sub.1R.sub.2N—(CH.sub.2).sub.n—SO.sub.2—(CH.sub.2).sub.q—, R.sub.1R.sub.2P(O)—, and R.sub.1R.sub.2R.sub.3Si—; m is 0 or 1, n and q are each independently an integer from 0 to 4, p is an integer from 1 to 4; R is hydrogen, a halogen-containing or not containing group selected from C1˜C6 alkyl, C2˜C6 alkenyl, C2˜C6 alkynyl, C3˜C6 cycloalkyl, and C3˜C6 cycloalkyl-C1˜C6 alkyl, 5- to 14-membered aryl, 5- to 14-membered aryl-C1˜C4 alkyl, or 5- to 14-membered heteroaryl, each of said 5- to 14-membered aryl, 5- to 14-membered aryl-C1˜C4 alkyl, or 5- to 14-membered heteroaryl is unsubstituted or substituted with 1˜3 groups independently selected from halogens; R.sub.1, R.sub.2, R.sub.3 are each independently hydrogen, nitro, hydroxy, amino, a halogen-containing or not containing group selected from C1˜C6 alkyl, C2˜C6 alkenyl, C2˜C6 alkynyl, C3˜C6 cycloalkyl, C1˜C6 alkoxy, C1˜C6 alkoxy-C1˜C6 alkyl, C1˜C6 alkoxycarbonyl, C1˜C6 alkylcarbonyl, C1˜C6 alkylcarbonyl-C1˜C6 alkyl, and C1˜C6 alkylcarbonyloxy, 5- to 14-membered aryl, 5- to 14-membered aryl-C1˜C6 alkyl, 5- to 14-membered aryloxy, 5- to 14-membered arylcarbonyl, 5- to 14-membered heteroaryl, 5- to 14-membered heteroaryl-C1˜C6 alkyl, 5- to 14-membered heteroaryloxy, 5- to 14-membered heteroarylcarbonyl, or 5- to 14-membered aliphatic heterocyclylcarbonyl, each of said 5- to 14-membered aryl, 5- to 14-membered aryl-C1˜C6 alkyl, 5- to 14-membered aryloxy, 5- to 14-membered arylcarbonyl, 5- to 14-membered heteroaryl, 5- to 14-membered heteroaryl-C1˜C6 alkyl, 5- to 14-membered heteroaryloxy, 5- to 14-membered heteroarylcarbonyl, or 5- to 14-membered aliphatic heterocyclylcarbonyl is unsubstituted or substituted with 1˜3 groups independently selected from halogen, cyano, nitro, hydroxy, carboxyl, sulfhydryl, amino, and a halogen-containing or not containing group selected from C1˜C6 alkyl, C3˜C6 cycloalkyl, C3˜C6 cycloalkyl-C1˜C6 alkyl, C2˜C6 alkenyl, C2˜C6 alkynyl, C1˜C6 alkoxy, C1˜C6 alkylcarbonyl, C1˜C8 alkoxycarbonyl, C1˜C8 alkylsulfonyl, C1˜C6 alkylamino, and C1˜C8 alkylcarbonyloxy; or R.sub.1R.sub.2N— is ##STR02164## the aryl is selected from ##STR02165## the heteroaryl is selected from ##STR02166## ##STR02167## ##STR02168## R′ is hydrogen, a fluoro-, chloro-, or bromo-containing or not containing group selected from C1˜C6 alkyl, C1˜C6 alkoxy-C1˜C6 alkyl, C1˜C6 alkoxycarbonyl, and C1˜C8 alkylcarbonyl, aliphatic heterocyclyl, phenyl, or benzyl; the aliphatic heterocyclyl is selected from ##STR02169## wherein the derivative is an agriculturally acceptable salt or a compound derivatized from 4-hydroxy of the pyridazine ring of the Formula I, including an ester, an oxime, a hydroxylamine and an ether thereof.

    5. The pyridazinol compound or a derivative thereof according to claim 1, wherein, X is halogenated C1˜C4 alkyl; A is selected from the group consisting of C1˜C4 alkyl, C2˜C4 alkenyl, C3˜C6 cycloalkyl, C3˜C6 cycloalkenyl, 5- to 14-membered aryl, 5- to 14-membered heteroaryl and 5- to 14-membered aliphatic heterocyclyl, each of which is unsubstituted or substituted; wherein, when being substituted, said C1˜C4 alkyl, C2˜C4 alkenyl, C3˜C6 cycloalkyl, or C3˜C6 cycloalkenyl is substituted with one or more substituents independently selected from R—O—(C═O)— and R.sub.1R.sub.2R.sub.3SiO—; when being substituted, said 5- to 14-membered aryl, 5- to 14-membered heteroaryl or 5- to 14-membered aliphatic heterocyclyl is substituted with one or more substituents independently selected from the group consisting of fluorine, chlorine, bromine, iodine, cyano, nitro, azido, a fluoro-, chloro- or bromo-containing or not containing group selected from C1˜C4 alkyl, C2˜C4 alkenyl, C2˜C4 alkynyl, C3˜C6 cycloalkyl, and C3˜C6 cycloalkyl-C1˜C4 alkyl, aryl, aryl-C1˜C4 alkyl, heteroaryl, heteroaryl-C1˜C4 alkyl, aliphatic heterocyclyl, each of said aryl, aryl-C1˜C4 alkyl, heteroaryl, heteroaryl-C1˜C4 alkyl, or aliphatic heterocyclyl is unsubstituted or substituted with 1˜3 groups independently selected from fluorine, chlorine, bromine, cyano, hydroxy, and a fluoro-, chloro- or bromo-containing or not containing group selected from C1˜C4 alkyl, C1˜C4 alkoxy, C1˜C4 alkoxycarbonyl, C1˜C4 alkylsulfonyl, and C1˜C4 alkylamino, R—O—(CH.sub.2).sub.n—, R—O—CH.sub.2—O—, R—S—(CH.sub.2).sub.n—, R—O—(CH.sub.2).sub.n—(C═O)—, R—O—(CH.sub.2).sub.n—(C═O)—O—, R—O—(C═O)—(CH.sub.2).sub.q—O—, R—O—(CH.sub.2).sub.n—(C═O)—(CH.sub.2).sub.q—S—, R—S—(CH.sub.2).sub.n—(C═O)—, R—(C═O)—(CH.sub.2).sub.n—, R—(C═O)—O—(CH.sub.2).sub.q—, R—(C═O)—(CH.sub.2).sub.n—O—, R—SO—(CH.sub.2).sub.n—, R—SO.sub.2—(CH.sub.2).sub.n—(O).sub.m—, R—SO.sub.2—(CH.sub.2).sub.n—NR.sub.3—, R.sub.1R.sub.2N—(C═O)—(CH.sub.2).sub.q—, R.sub.1R.sub.2N—(C═O)—(CH.sub.2).sub.q—O—, R.sub.1R.sub.2N—(C™0)(NR.sub.3).sub.m—, R.sub.1R.sub.2N—(CH.sub.2).sub.n—, R.sub.1R.sub.2N—(CH.sub.2).sub.n—SO.sub.2—(CH.sub.2).sub.q—, R.sub.1R.sub.2P(O), and R.sub.1R.sub.2R.sub.3Si—; m is 0 or 1, n and q are each independently an integer from 0, 1, 2 and 3, p is an integer from 1, 2 and 3; R is hydrogen, a halogen-containing or not containing group selected from C1˜C4 alkyl, C2˜C4 alkenyl, C2˜C6 alkynyl, C3˜C6 cycloalkyl, and C3˜C6 cycloalkyl-C1˜C4 alkyl, 5- to 14-membered aryl, 5- to 14-membered aryl-C1˜C2 alkyl, or 5- to 6-membered heteroaryl, each of said 5- to 14-membered aryl, 5- to 14-membered aryl-C1˜C2 alkyl, or 5- to 6-membered heteroaryl is unsubstituted or substituted with 1˜3 groups independently selected from fluorine, chlorine, and bromine; R.sub.1, R.sub.2, R.sub.3 are each independently hydrogen, a fluoro-, chloro- or bromo-containing or not containing group selected from C1˜C4 alkyl, C2˜C4 alkenyl, C2˜C4 alkynyl, C3˜C6 cycloalkyl, C1˜C4 alkoxy, C1˜C4 alkoxyC1˜C4 alkyl, C1˜C4 alkoxycarbonyl, C1˜C4 alkylcarbonyl, C1˜C4 alkylcarbonyl-C1˜C4 alkyl, and C1˜C4 alkylcarbonyloxy, 5- to 14-membered aryl, 5- to 14-membered aryloxy, 5- to 14-membered arylcarbonyl, 5- to 6-membered heteroaryl, 5- to 6-membered heteroaryl-C1˜C4 alkyl, or 5- to 6-membered heteroarylcarbonyl, each of said 5- to 14-membered aryl, 5- to 14-membered aryloxy, 5- to 14-membered arylcarbonyl, 5- to 6-membered heteroaryl, 5- to 6-membered heteroaryl-C1˜C4 alkyl, or 5- to 6-membered heteroarylcarbonyl is unsubstituted or substituted with 1˜3 groups independently selected from fluorine, chlorine, bromine, C1˜C4 alkyl, C1˜C4 alkoxy, C1˜C4 alkylamino, and C3˜C6 cycloalkyl; or R.sub.1R.sub.2N— is ##STR02170## the aryl is selected from ##STR02171## the heteroaryl is selected from ##STR02172## ##STR02173## ##STR02174## R′ is hydrogen, a fluoro-, chloro-, or bromo-containing or not containing group selected from C1˜C4 alkyl, C1˜C4 alkoxy-C1˜C4 alkyl, C1˜C4 alkoxycarbonyl, and C1˜C4 alkylcarbonyl, ##STR02175## phenyl, or benzyl; the aliphatic heterocyclyl is selected from ##STR02176## wherein the derivative is an agriculturally acceptable salt or a compound derivatized from 4-hydroxy of the pyridazine ring of the Formula I, including an ester, an oxime, a hydroxylamine and an ether thereof.

    6. The pyridazinol compound or a derivative thereof according to claim 1, wherein, X is CH.sub.2F, CHF.sub.2, CF.sub.3, or CF.sub.2CF.sub.3; A is methyl, ethyl, ##STR02177## unsubstituted or substituted 5- to 14-membered aryl, unsubstituted or substituted 5- to 14-membered heteroaryl, or unsubstituted or substituted 5- to 14-membered aliphatic heterocyclyl; wherein, said substituted 5- to 14-membered aryl, substituted 5- to 14-membered heteroaryl or substituted 5- to 14-membered aliphatic heterocyclyl is the 5- to 14-membered aryl, 5- to 14-membered heteroaryl, or 5- to 14-membered aliphatic heterocyclyl, which is substituted with one or more substituents independently selected from the group consisting of fluorine, chlorine, bromine, iodine, cyano, nitro, azido, a fluoro-, chloro- or bromo-containing or not containing group selected from C1˜C4 alkyl, C2˜C4 alkenyl, C2˜C4 alkynyl, C3˜C6 cycloalkyl, and C3˜C6 cycloalkyl-C1˜C2 alkyl, phenyl, pyrrolyl, furyl, imidazolyl, pyrazolyl, oxazolyl, isoxazolyl, thiazolyl, oxadiazolyl, thiadiazolyl, triazolyl, pyridyl, pyrazinyl, pyrimidinyl, benzyl, tetrahydropyranyl, thienylmethyl, each of said phenyl, pyrrolyl, furyl, imidazolyl, pyrazolyl, oxazolyl, isoxazolyl, thiazolyl, oxadiazolyl, thiadiazolyl, triazolyl, pyridyl, pyrazinyl, pyrimidinyl, benzyl, tetrahydropyranyl, tbienylmethyl is unsubstituted or substituted with 1˜3 groups independently selected from fluorine, chlorine, bromine, cyano, hydroxy, and a fluoro-, chloro- or bromo-containing or not containing group selected from C1˜C4 alkyl, C1˜C4 alkoxy, C1˜C4 alkoxycarbonyl, C1˜C4 alkylsulfonyl, and C1˜C4 alkylamino, R—O—, R—O—CH.sub.2—, R—O—CH.sub.2CH.sub.2—, R—O—CH.sub.2—O—, R—O—(C═O)—, R—O—CH.sub.2—(C═O)—, R—O—CH.sub.2—(C═O)—O—, R—O—(C═O)—CH.sub.2—O—, R—O—(C═O)—CH.sub.2CH.sub.2—O—, R—O—(C═O)—CH.sub.2—S—, R—O—CH.sub.2—(C═O)—S—, R—O—CH.sub.2—(C═O)—CH.sub.2—S—, R—S—CH.sub.2—, R—S—, R—S—(C═O)—, R—S—CH.sub.2—(C═O)—, R—(C═O)—CH.sub.2—, R—(C═O)—, R—(C═O)—O—CH.sub.2—, R—(C═O)—CH.sub.2—O—, R—(C═O)—CH.sub.2CH.sub.2—O—, R—(C═O)—O—, R—SO—CH.sub.2—, R—SO—, R—SO.sub.2—CH.sub.2—O—, R—SO.sub.2—CH.sub.2—, R—SO.sub.2—O—, R—SO.sub.2—, R—SO.sub.2—CH.sub.2—NR.sub.3—, R—SO.sub.2—NR.sub.3—, R.sub.1R.sub.2N—CH.sub.2—, R.sub.1R.sub.2N—, R.sub.1R.sub.2N—(C═O)—CH.sub.2—, R.sub.1R.sub.2N—(C═O)—CH.sub.2—O—, R.sub.1R.sub.2N—(C═O)—, R.sub.1R.sub.2N—(C═O)—NR.sub.3—, R.sub.1R.sub.2N—CH.sub.2—SO.sub.2—, R.sub.1R.sub.2N—CH.sub.2—SO.sub.2—CH.sub.2—, R.sub.1R.sub.2N—SO.sub.2—CH.sub.2—, R.sub.1R.sub.2N—SO.sub.2—, R.sub.1R.sub.2P(O)—, and R.sub.1R.sub.2R.sub.3Si—; R is hydrogen, a fluoro-, chloro-, or bromo-containing or not containing group selected from C1˜C4 alkyl, C2˜C4 alkenyl, C2˜C4 alkynyl, C3˜C8 cycloalkyl, and C3˜C6 cycloalkyl-C1˜C2 alkyl, phenyl, benzyl, or thienyl, each of said phenyl, benzyl, or thienyl is unsubstituted or substituted with 1-3 groups independently selected from fluorine, chlorine, and bromine; R.sub.1, R.sub.2, R.sub.3 are each independently is hydrogen, a fluoro-, chloro-, or bromo-containing or not containing group selected from C1˜C4 alkyl, C2˜C4 alkenyl, C2˜C4 alkynyl, C3˜C8 cycloalkyl, C1˜C4 alkoxy, C1˜C4 alkoxy-C1˜C2 alkyl, C1˜C4 alkoxycarbonyl, C1˜C4 alkylcarbonyl, C1˜C4 alkylcarbonyl-C1˜C2 alkyl, and C1˜C4 alkylcarbonyloxy, phenyl, naphthyl, phenoxy, furyl, thienyl, thiadiazolyl, thienylmethyl, pyrazolylmethyl, benzoyl, or pyridinylformyl, each of said phenyl, naphthyl, phenoxy, furyl, thienyl, thiadiazolyl, thienylmethyl, pyrazolylmethyl, benzoyl, or pyridinylformyl is unsubstituted or substituted with 1˜3 groups independently selected from fluorine, chlorine, bromine, C1˜C4 alkyl, C3˜C6 cycloalkyl, C1˜C4 alkoxy, and C1˜C4 alkylamino; or R.sub.1R.sub.2N— is ##STR02178## the 5- to 14-membered aryl is selected from ##STR02179## the heteroaryl is selected from ##STR02180## ##STR02181## ##STR02182## R′ is hydrogen, a fluoro-chloro-, or bromo-containing or not containing group selected from C1˜C4 alkyl, C1˜C4 alkoxy-C1˜C2 alkyl, C1˜C4 alkoxycarbonyl, and C1˜C4 alkylcarbonyl, ##STR02183## phenyl, or benzyl; the aliphatic heterocyclyl is ##STR02184## wherein the derivative is an agriculturally acceptable salt or a compound derivatized from 4-hydroxy of the pyridazine ring of the Formula I, including an ester, an oxime, a hydroxylamine and an ether thereof.

    7. The pyridazinol compound or a derivative thereof according to claim 1, wherein, the compound is selected from those of Formula I, wherein X and A are shown below: TABLE-US-00007 No. X A 1 CF.sub.3 embedded image 2 CF.sub.3 embedded image 3 CF.sub.3 embedded image 4 CF.sub.3 embedded image 5 CF.sub.3 embedded image 6 CF.sub.3 embedded image 7 CF.sub.3 embedded image 8 CF.sub.3 embedded image 9 CF.sub.3 embedded image 10 CF.sub.3 embedded image 11 CF.sub.3 embedded image 12 CF.sub.3 embedded image 13 CF.sub.3 embedded image 14 CF.sub.3 embedded image 15 CF.sub.3 embedded image 16 CF.sub.3 embedded image 17 CF.sub.3 embedded image 18 CF.sub.3 embedded image 19 CF.sub.3 embedded image 20 CF.sub.3 embedded image 21 CF.sub.3 embedded image 22 CF.sub.3 embedded image 23 CF.sub.3 embedded image 24 CF.sub.3 embedded image 25 CF.sub.3 embedded image 26 CF.sub.3 embedded image 27 CF.sub.3 embedded image 28 CF.sub.3 embedded image 29 CF.sub.3 embedded image 30 CF.sub.3 embedded image 31 CF.sub.3 embedded image 32 CF.sub.3 embedded image 33 CF.sub.3 embedded image 34 CF.sub.3 embedded image 35 CF.sub.3 embedded image 36 CF.sub.3 embedded image 37 CF.sub.3 embedded image 38 CF.sub.3 embedded image 39 CF.sub.3 embedded image 40 CF.sub.3 embedded image 41 CF.sub.3 embedded image 42 CF.sub.3 embedded image 43 CF.sub.3 embedded image 44 CF.sub.3 embedded image 45 CF.sub.3 embedded image 46 CF.sub.3 embedded image 47 CF.sub.3 embedded image 48 CF.sub.3 embedded image 49 CF.sub.3 embedded image 50 CF.sub.3 embedded image 51 CF.sub.3 embedded image 52 CF.sub.3 embedded image 53 CF.sub.3 embedded image 54 CF.sub.3 embedded image 55 CF.sub.3 embedded image 56 CF.sub.3 embedded image 57 CF.sub.3 embedded image 58 CF.sub.3 embedded image 59 CF.sub.3 embedded image 60 CF.sub.3 embedded image 61 CF.sub.3 embedded image 62 CF.sub.3 embedded image 63 CF.sub.3 embedded image 64 CF.sub.3 embedded image 65 CF.sub.3 embedded image 66 CF.sub.3 embedded image 67 CF.sub.3 embedded image 68 CF.sub.3 embedded image 69 CF.sub.3 embedded image 70 CF.sub.3 embedded image 71 CF.sub.3 embedded image 72 CF.sub.3 embedded image 73 CF.sub.3 embedded image 74 CF.sub.3 embedded image 75 CF.sub.3 embedded image 76 CF.sub.3 embedded image 77 CF.sub.3 embedded image 78 CF.sub.3 embedded image 79 CF.sub.3 embedded image 80 CF.sub.3 embedded image 81 CF.sub.3 embedded image 82 CF.sub.3 embedded image 83 CF.sub.3 embedded image 84 CF.sub.3 embedded image 85 CF.sub.3 embedded image 86 CF.sub.3 embedded image 87 CF.sub.3 embedded image 88 CF.sub.3 embedded image 89 CF.sub.3 embedded image 90 CF.sub.3 embedded image 91 CF.sub.3 embedded image 92 CF.sub.3 embedded image 93 CF.sub.3 embedded image 94 CF.sub.3 embedded image 95 CF.sub.3 embedded image 96 CF.sub.3 embedded image 97 CF.sub.3 embedded image 98 CF.sub.3 embedded image 99 CF.sub.3 embedded image 100 CF.sub.3 embedded image 101 CF.sub.3 embedded image 102 CF.sub.3 embedded image 103 CF.sub.3 embedded image 104 CF.sub.3 embedded image 105 CF.sub.3 embedded image 106 CF.sub.3 embedded image 107 CF.sub.3 embedded image 108 CF.sub.3 embedded image 109 CF.sub.3 embedded image 110 CF.sub.3 embedded image 111 CF.sub.3 embedded image 112 CF.sub.3 embedded image 113 CF.sub.3 embedded image 114 CF.sub.3 embedded image 115 CF.sub.3 embedded image 116 CF.sub.3 embedded image 117 CF.sub.3 embedded image 118 CF.sub.3 embedded image 119 CF.sub.3 embedded image 120 CF.sub.3 embedded image 121 CF.sub.3 embedded image 122 CF.sub.3 embedded image 123 CF.sub.3 embedded image 124 CF.sub.3 embedded image 125 CF.sub.3 embedded image 126 CF.sub.3 embedded image 127 CF.sub.3 embedded image 128 CF.sub.3 embedded image 129 CF.sub.3 embedded image 130 CF.sub.3 embedded image 131 CF.sub.3 embedded image 132 CF.sub.3 embedded image 133 CF.sub.3 embedded image 134 CF.sub.3 embedded image 135 CF.sub.3 embedded image 136 CF.sub.3 embedded image 137 CF.sub.3 embedded image 138 CF.sub.3 embedded image 139 CF.sub.3 embedded image 140 CF.sub.3 embedded image 141 CF.sub.3 embedded image 142 CF.sub.3 embedded image 143 CF.sub.3 embedded image 144 CF.sub.3 embedded image 145 CF.sub.3 embedded image 146 CF.sub.3 embedded image 147 CF.sub.3 embedded image 148 CF.sub.3 embedded image 149 CF.sub.3 embedded image 150 CF.sub.3 embedded image 151 CF.sub.3 embedded image 152 CF.sub.3 embedded image 153 CF.sub.3 embedded image 154 CF.sub.3 embedded image 155 CF.sub.3 embedded image 156 CF.sub.3 embedded image 157 CF.sub.3 embedded image 158 CF.sub.3 embedded image 159 CF.sub.3 embedded image 160 CF.sub.3 embedded image 161 CF.sub.3 embedded image 162 CF.sub.3 embedded image 163 CF.sub.3 embedded image 164 CF.sub.3 embedded image 165 CF.sub.3 embedded image 166 CF.sub.3 embedded image 167 CF.sub.3 embedded image 168 CF.sub.3 embedded image 169 CF.sub.3 embedded image 170 CF.sub.3 embedded image 171 CF.sub.3 embedded image 172 CF.sub.3 embedded image 173 CF.sub.3 embedded image 174 CF.sub.3 embedded image 175 CF.sub.3 embedded image 176 CF.sub.3 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embedded image 1165 CF.sub.3 embedded image 1166 CF.sub.3 embedded image 1167 CF.sub.3 embedded image 1168 CF.sub.3 embedded image 1169 CF.sub.3 embedded image 1170 CF.sub.3 embedded image 1171 CF.sub.3 embedded image 1172 CF.sub.3 embedded image 1173 CF.sub.3 embedded image 1174 CF.sub.3 embedded image 1175 CF.sub.3 embedded image 1176 CF.sub.3 embedded image 1177 CF.sub.3 embedded image 1178 CF.sub.3 embedded image 1179 CF.sub.3 embedded image 1180 CF.sub.3 embedded image 1181 CF.sub.3 embedded image 1182 CF.sub.3 embedded image 1183 CF.sub.3 embedded image 1184 CF.sub.3 embedded image 1185 CF.sub.3 embedded image 1186 CF.sub.3 embedded image 1187 CF.sub.3 embedded image 1188 CF.sub.3 embedded image 1189 CF.sub.3 embedded image 1190 CF.sub.3 embedded image 1191 CF.sub.3 embedded image 1192 CF.sub.3 embedded image 1193 CF.sub.3 embedded image 1194 CF.sub.3 embedded image 1195 CF.sub.3 embedded image 1196 CF.sub.3 embedded image 1197 CF.sub.3 embedded image 1198 CF.sub.3 embedded image 1199 CF.sub.3 embedded image 1200 CF.sub.3 embedded image 1201 CF.sub.3 embedded image 1202 CF.sub.3 embedded image 1203 CF.sub.3 embedded image 1204 CF.sub.3 embedded image 1205 CF.sub.3 embedded image 1206 CF.sub.3 embedded image 1207 CF.sub.3 embedded image 1208 CF.sub.3 embedded image 1209 CF.sub.3 embedded image 1210 CF.sub.3 embedded image 1211 CF.sub.3 embedded image 1212 CF.sub.3 embedded image 1213 CF.sub.3 embedded image 1214 CF.sub.3 embedded image 1215 CF.sub.3 embedded image 1216 CF.sub.3 embedded image 1217 CF.sub.3 embedded image 1218 CF.sub.3 embedded image 1219 CF.sub.3 embedded image 1220 CF.sub.3 embedded image 1221 CF.sub.3 embedded image 1222 CF.sub.3 embedded image 1223 CF.sub.3 embedded image 1224 CF.sub.3 embedded image 1225 CF.sub.3 embedded image 1226 CF.sub.3 embedded image 1227 CF.sub.3 embedded image 1228 CF.sub.3 embedded image 1229 CF.sub.3 embedded image 1230 CF.sub.3 embedded image 1231 CF.sub.3 embedded image 1232 CF.sub.3 embedded image 1233 CF.sub.3 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embedded image 1303 CF.sub.3 embedded image 1304 CF.sub.3 embedded image 1305 CF.sub.3 embedded image 1306 CF.sub.3 embedded image 1307 CF.sub.3 embedded image 1308 CF.sub.3 embedded image 1309 CF.sub.3 embedded image 1310 CF.sub.3 embedded image 1311 CF.sub.3 embedded image 1312 CF.sub.3 embedded image 1313 CF.sub.3 embedded image 1314 CF.sub.3 embedded image 1315 CF.sub.3 embedded image 1316 CF.sub.3 embedded image 1317 CF.sub.3 embedded image 1318 CF.sub.3 embedded image 1319 CF.sub.3 embedded image 1320 CF.sub.3 embedded image 1321 CF.sub.3 embedded image 1322 CF.sub.3 embedded image 1323 CF.sub.3 embedded image 1324 CF.sub.3 embedded image 1325 CF.sub.3 embedded image 1326 CF.sub.3 embedded image 1327 CF.sub.3 embedded image 1328 CF.sub.3 embedded image 1329 CF.sub.3 embedded image 1330 CF.sub.3 embedded image 1331 CF.sub.3 embedded image 1332 CF.sub.3 embedded image 1333 CF.sub.3 embedded image 1334 CF.sub.3 embedded image 1335 CF.sub.3 embedded image 1336 CF.sub.3 embedded image 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embedded image 1372 CF.sub.3 embedded image 1373 CF.sub.3 embedded image 1374 CF.sub.3 embedded image 1375 CF.sub.3 embedded image 1376 CF.sub.3 embedded image 1377 CF.sub.3 embedded image 1378 CF.sub.3 embedded image 1379 CF.sub.3 embedded image 1380 CF.sub.3 embedded image 1381 CF.sub.3 embedded image 1382 CF.sub.3 embedded image 1383 CF.sub.3 embedded image 1384 CF.sub.3 embedded image 1385 CF.sub.3 embedded image 1386 CF.sub.3 embedded image 1387 CF.sub.3 embedded image 1388 CF.sub.3 embedded image 1389 CF.sub.3 embedded image 1390 CF.sub.3 embedded image 1391 CF.sub.3 embedded image 1392 CF.sub.3 embedded image 1393 CF.sub.3 embedded image 1394 CF.sub.3 embedded image 1395 CF.sub.3 embedded image 1396 CF.sub.3 embedded image 1397 CF.sub.3 embedded image 1398 CF.sub.3 embedded image 1399 CF.sub.3 embedded image 1400 CF.sub.3 embedded image 1401 CF.sub.3 embedded image 1402 CF.sub.3 embedded image 1403 CF.sub.3 embedded image 1404 CF.sub.3 embedded image 1405 CF.sub.3 embedded image 1406 CF.sub.3 embedded image 1407 CF.sub.3 embedded image 1408 CF.sub.3 embedded image 1409 CF.sub.3 embedded image 1410 CF.sub.3 embedded image 1411 CF.sub.3 embedded image 1412 CF.sub.3 embedded image 1413 CF.sub.3 embedded image 1414 CF.sub.3 embedded image 1415 CF.sub.3 embedded image 1416 CF.sub.3 embedded image 1417 CF.sub.3 embedded image 1418 CF.sub.3 embedded image 1419 CF.sub.3 embedded image 1420 CF.sub.3 embedded image 1421 CF.sub.3 embedded image 1422 CF.sub.3 embedded image 1423 CF.sub.3 embedded image 1424 CF.sub.3 embedded image 1425 CF.sub.3 embedded image 1426 CF.sub.3 embedded image 1427 CF.sub.3 embedded image 1428 CF.sub.3 embedded image 1429 CF.sub.3 embedded image 1430 CF.sub.3 embedded image 1431 CF.sub.3 embedded image 1432 CF.sub.3 embedded image 1433 CF.sub.3 embedded image 1434 CF.sub.3 embedded image 1435 CF.sub.3 embedded image 1436 CF.sub.3 embedded image 1437 CF.sub.3 embedded image 1438 CF.sub.3 embedded image 1439 CF.sub.3 embedded image 1440 CF.sub.3 embedded image 1441 CF.sub.3 embedded image 1442 CF.sub.3 embedded image 1443 CF.sub.3 embedded image 1444 CF.sub.3 embedded image 1445 CF.sub.3 embedded image 1446 CF.sub.3 embedded image 1447 CF.sub.3 embedded image 1448 CF.sub.3 embedded image 1449 CF.sub.3 embedded image 1450 CF.sub.3 embedded image 1451 CF.sub.3 embedded image 1452 CF.sub.3 embedded image 1453 CF.sub.3 embedded image 1454 CF.sub.3 embedded image 1455 CF.sub.3 embedded image 1456 CF.sub.3 embedded image 1457 CF.sub.3 embedded image 1458 CF.sub.3 embedded image 1459 CF.sub.3 embedded image 1460 CF.sub.3 embedded image 1461 CF.sub.3 embedded image 1462 CF.sub.3 embedded image 1463 CF.sub.3 embedded image 1464 CF.sub.3 embedded image 1465 CF.sub.3 embedded image 1466 CF.sub.3 embedded image 1467 OCH.sub.3 embedded image 1468 CF.sub.3 embedded image 1469 CF.sub.3 embedded image 1470 CF.sub.2CF.sub.3 embedded image 1471 CH.sub.2F embedded image 1472 CHF.sub.2 embedded image 1473 CF.sub.2CF.sub.3 embedded image 1474 CH.sub.2F embedded image 1475 CHF.sub.2 embedded image 1476 CF.sub.2CF.sub.3 embedded image 1477 CH.sub.2F embedded image 1478 OCHF.sub.2 embedded image 1479 CF.sub.2CF.sub.3 embedded image 1480 CF.sub.2CF.sub.3 embedded image 1481 CF.sub.2CF.sub.3 embedded image 1482 CF.sub.2CF.sub.3 embedded image 1483 Ph embedded image 1484 CF.sub.2CF.sub.3 embedded image 1485 CF.sub.2CF.sub.3 embedded image 1486 CF.sub.2CF.sub.3 embedded image 1487 CN embedded image 1488 CF.sub.2CF.sub.3 embedded image 1489 CF.sub.2CF.sub.3 embedded image 1490 CF.sub.2CF.sub.3 embedded image 1491 CF.sub.2CF.sub.3 embedded image 1492 CF.sub.2CF.sub.3 embedded image 1493 CF.sub.3 embedded image 1494 CF.sub.3 embedded image 1495 CF.sub.3 embedded image 1496 CF.sub.3 embedded image 1497 CF.sub.3 embedded image 1498 CF.sub.3 embedded image 1499 CF.sub.3 embedded image 1500 CF.sub.3 embedded image 1501 OCF.sub.3 embedded image 1502 CF.sub.3 embedded image 1503 CF.sub.3 embedded image 1504 CF.sub.3 embedded image 1505 CF.sub.3 embedded image 1506 CF.sub.3 embedded image 1507 CONH.sub.2 embedded image 1508 CF.sub.3 embedded image 1509 CF.sub.3 embedded image 1510 CF.sub.3 embedded image 1511 CF.sub.3 embedded image 1512 CF.sub.3 embedded image 1513 Ph embedded image 1514 CF.sub.3 embedded image 1515 CF.sub.3 embedded image 1516 NH.sub.2 embedded image 1517 CF.sub.3 embedded image 1518 CF.sub.3 embedded image 1519 CF.sub.3 embedded image 1520 CF.sub.3 embedded image 1521 CF.sub.3 embedded image 1522 CF.sub.3 embedded image 1523 CF.sub.3 embedded image 1524 CF.sub.3 embedded image 1525 CF.sub.3 Me 1526 CF.sub.3 embedded image 1527 OH embedded image 1528 CF.sub.3 embedded image 1529 CF.sub.3 embedded image 1530 CF.sub.3 embedded image 1531 CF.sub.3 embedded image 1532 CF.sub.3 embedded image 1533 CF.sub.3 Et 1534 OCF.sub.3 embedded image 1535 CF.sub.3 embedded image 1536 CN embedded image 1537 CF.sub.3 embedded image 1538 CF.sub.3 embedded image 1539 CF.sub.3 embedded image 1540 CF.sub.3 embedded image 1541 CF.sub.3 embedded image 1542 CF.sub.3 embedded image 1543 CF.sub.2CF.sub.3 embedded image 1544 CF.sub.3 embedded image 1545 CF.sub.3 embedded image 1546 CF.sub.3 embedded image 1547 CHF.sub.2 embedded image 1548 CF.sub.3 embedded image 1549 CF.sub.3 embedded image

    8. The derivative of the pyridazinol compound according to claim 1, which has a structure as shown in Formula I-1: ##STR03732## wherein, M is (thio)formyl, C1˜C18 alkyl(thio)carbonyl, wherein said (thio)formyl or C1˜C18 alkyl(thio)carbonyl is unsubstituted or substituted with a substituent independently selected from the group consisting of: halogen, amino, C3˜C8 cycloalkyl, C1˜C8 alkoxycarbonyl, C1˜C8 alkylcarbonyloxy, C1˜C8 alkylcarbonyl, hydroxy(methyl)phosphinyl, and an unsubstituted or halogenated or C1˜C8 alkoxy substituted group selected from phenyl, phenylsulfanyl, phenyloxy, and benzyloxy; an unsubstituted or phenyl substituted group of C1˜C18 alkoxy(thio)carbonyl or C1˜C18 alkylsulfanyl(thio)carbonyl; C3˜C8 cycloalkylsulfanyl(thio)carbonyl; phenyl-C1˜C8 alkylsulfanyl(thio)carbonyl; C2˜C8 alkenyl(thio)carbonyl, wherein said C2˜C8 alkenyl(thio)carbonyl unsubstituted or substituted with a substituent selected from the group consisting of: C1˜C8 alkoxy, phenyl and halogenated phenyl; (thio)benzoyl, wherein said (thio)benzoyl is unsubstituted or substituted with a substituent selected from the group consisting of: halogen, hydroxy, C1˜C8 alkyl, C1˜C8 alkoxy, cyano, halogenated C1˜C8 alkoxy, C1˜CS alkylcarbonyloxy, C1˜C8 alkylcarbonylamino, amino and amino substituted with 1 or 2˜C1˜C8 alkyl; halogenated sulfanyl formyl; 3- to 8-membered heterocyclyl(thio)carbonyl, wherein said 3- to 8-membered heterocyclyl(thio)carbonyl is unsubstituted or substituted with a substituent selected from C1˜C8 alkyl, halogen, and C1˜C8 alkylsulfanyl; fused 5- to 14-membered bicyclic or tricyclic heterocyclyl(thio)carbonyl; amino(thio)formyl, wherein said amino(thio)formyl is unsubstituted or substituted with a substituent selected from C1˜C8 alkyl and C1˜C8 alkoxy; an unsubstituted or halogen or C1˜C8 alkylsulfanyl substituted group selected from C1˜C8 alkylsulfoxide, C1˜C8 alkylsulfonyl, and C3˜C8 cycloalkylsulfonyl; phenylsulfonyl, benzylsulfonyl, naphthylsulfonyl, wherein each of said phenylsulfonyl, benzylsulfonyl or naphthylsulfonyl is unsubstituted or substituted with a substituent independently selected from the group consisting of: halogen, nitro, C1˜C8 alkyl, halogenated C1˜C8 alkyl, halogenated C1˜C8 alkoxy, C1˜C8 alkylcarbonyl, C1˜C8 alkylsulfonyl, aminoformyl, phenoxy and halogenated phenoxy; 5- to 10-membered heteroarylsulfonyl, wherein said 5- to 10-membered heteroarylsulfonyl is unsubstituted or substituted with C1˜C8 alkyl or phenoxy; C1˜C8 alkylaminosulfonyl that is unsubstituted or substituted with halogen; di(C1˜C8 alkyl) phosphoryl; C.sub.1-18alkyl, wherein said C.sub.1-18alkyl is unsubstituted or substituted with a substituent independently selected from C1˜C8 alkoxycarbonyl and C1˜C8 alkoxycarbonyloxy; an unsubstituted or halogenated or C1˜C8 alkoxy substituted group selected from phenyl, benzyl, and benzoyl-C1˜C8 alkyl; ##STR03733## wherein, R.sub.11 and R.sub.22 are independently selected from hydrogen, C1˜C18 alkyl, wherein said C1˜C18 alkyl is unsubstituted or substituted with a substituent selected from C1˜C8 alkoxy and C1˜C8 alkylsulfanyl, and an unsubstituted or halogenated C1˜C8 alkyl substituted group selected from phenyl and 5- to 6-membered heteroaryl; or R.sub.1-1 and R.sub.12 forms a 5- to 6-membered saturated carbocyclic ring or a 5- to 6-membered saturated heterocyclic ring; R.sub.11′ and R.sub.22′ independently is C1˜C18 alkyl; Het is selected from ##STR03734## Ra and Rb independently are hydrogen or C1˜C6 alkyl; X and A are as defined in claim 1.

    9. The derivative of the pyridazinol compound according to claim 8, wherein the pyridazinol compound is selected from the compounds having a structure of ##STR03735## wherein X, M, and A are shown below: TABLE-US-00008 No. X M A 1-1 CF.sub.3 embedded image embedded image 1-2 CF.sub.3 embedded image embedded image 1-3 CF.sub.3 embedded image embedded image 1-4 CF.sub.3 embedded image embedded image 1-5 CF.sub.3 embedded image embedded image 1-6 CF.sub.3 embedded image embedded image 1-7 CF.sub.3 embedded image embedded image 1-8 CF.sub.3 embedded image embedded image 1-9 CF.sub.3 embedded image embedded image 1-10 CF.sub.3 embedded image embedded image 1-11 CF.sub.3 embedded image embedded image 1-12 CF.sub.3 embedded image embedded image 1-13 CF.sub.3 embedded image embedded image 1-14 CF.sub.3 embedded image embedded image 1-15 CF.sub.3 embedded image embedded image 1-16 CF.sub.3 embedded image embedded image 1-17 CF.sub.3 embedded image embedded image 1-18 CF.sub.3 embedded image embedded image 1-19 CF.sub.3 embedded image embedded image 1-20 CF.sub.3 embedded image embedded image 1-21 CF.sub.3 embedded image embedded image 1-22 CF.sub.3 embedded image embedded image 1-23 CF.sub.3 embedded image embedded image 1-24 CF.sub.3 embedded image embedded image 1-25 CF.sub.3 embedded image embedded image 1-26 CF.sub.3 embedded image embedded image 1-27 CF.sub.3 embedded image embedded image 1-28 CF.sub.3 embedded image embedded image 1-29 CF.sub.3 embedded image embedded image 1-30 CF.sub.3 embedded image embedded image 1-31 CF.sub.3 embedded image embedded image 1-32 CF.sub.3 embedded image embedded image 1-33 CF.sub.3 embedded image embedded image 1-34 CF.sub.3 embedded image embedded image 1-35 CF.sub.3 embedded image embedded image 1-36 CF.sub.3 embedded image embedded image 1-37 CF.sub.3 embedded image embedded image 1-38 CF.sub.3 embedded image embedded image 1-39 CF.sub.3 embedded image embedded image 1-40 CF.sub.3 embedded image embedded image 1-41 CF.sub.3 embedded image embedded image 1-42 CF.sub.3 embedded image embedded image 1-43 CF.sub.3 embedded image embedded image 1-44 CF.sub.3 embedded image embedded image 1-45 CF.sub.3 embedded image embedded image 1-46 CF.sub.3 embedded image embedded image 1-47 CF.sub.3 embedded image embedded image 1-48 CF.sub.3 embedded image embedded image 1-49 CF.sub.3 embedded image embedded image 1-50 CF.sub.3 embedded image embedded image 1-51 CF.sub.3 embedded image embedded image 1-52 CF.sub.3 embedded image embedded image 1-53 CF.sub.3 embedded image embedded image 1-54 CF.sub.3 embedded image embedded image 1-55 CF.sub.3 embedded image embedded image 1-56 CF.sub.3 embedded image embedded image 1-57 CF.sub.3 embedded image embedded image 1-58 CF.sub.3 embedded image embedded image 1-59 CF.sub.3 embedded image embedded image 1-60 CF.sub.3 embedded image embedded image 1-61 CF.sub.3 embedded image embedded image 1-62 CF.sub.3 embedded image embedded image 1-63 CF.sub.3 embedded image embedded image 1-64 CF.sub.3 embedded image embedded image 1-65 CF.sub.3 embedded image embedded image 1-66 CF.sub.3 embedded image embedded image 1-67 CF.sub.3 embedded image embedded image 1-68 CF.sub.3 embedded image embedded image 1-69 CF.sub.3 embedded image embedded image 1-70 CF.sub.3 embedded image embedded image 1-71 CF.sub.3 embedded image embedded image 1-72 CF.sub.3 embedded image embedded image 1-73 CF.sub.3 embedded image embedded image 1-74 CF.sub.3 embedded image embedded image 1-75 CF.sub.3 embedded image embedded image 1-76 CF.sub.3 embedded image embedded image 1-77 CF.sub.3 embedded image embedded image 1-78 CF.sub.3 embedded image embedded image 1-79 CF.sub.3 embedded image embedded image 1-80 CF.sub.3 embedded image embedded image 1-81 CF.sub.3 embedded image embedded image 1-82 CF.sub.3 embedded image embedded image 1-83 CF.sub.3 embedded image embedded image 1-84 CF.sub.3 embedded image embedded image 1-85 CF.sub.3 embedded image embedded image 1-86 CF.sub.3 embedded image embedded image 1-87 CF.sub.3 embedded image embedded image 1-88 CF.sub.3 embedded image embedded image 1-89 CF.sub.3 embedded image embedded image 1-90 CF.sub.3 embedded image embedded image 1-91 CF.sub.3 embedded image embedded image 1-92 CF.sub.3 embedded image embedded image 1-93 CF.sub.3 embedded image embedded image 1-94 CF.sub.3 embedded image embedded image 1-95 CF.sub.3 embedded image embedded image 1-96 CF.sub.3 embedded image embedded image 1-97 CF.sub.3 embedded image embedded image 1-98 CF.sub.3 embedded image embedded image 1-99 CF.sub.3 embedded image embedded image 1-100 CF.sub.3 embedded image embedded image 1-101 CF.sub.3 embedded image embedded image 1-102 CF.sub.3 embedded image embedded image 1-103 CF.sub.3 embedded image embedded image 1-104 CF.sub.3 embedded image embedded image 1-105 CF.sub.3 embedded image embedded image 1-106 CF.sub.3 embedded image embedded image 1-107 CF.sub.3 embedded image embedded image 1-108 CF.sub.3 embedded image embedded image 1-109 CF.sub.3 embedded image embedded image 1-110 CF.sub.3 embedded image embedded image 1-111 CF.sub.3 embedded image embedded image 1-112 CF.sub.3 embedded image embedded image 1-113 CF.sub.3 embedded image embedded image 1-114 CF.sub.3 embedded image embedded image 1-115 CF.sub.3 embedded image embedded image 1-116 CF.sub.3 embedded image embedded image 1-117 CF.sub.3 embedded image embedded image 1-118 CF.sub.3 embedded image embedded image 1-119 CF.sub.3 embedded image embedded image 1-120 CF.sub.3 embedded image embedded image 1-121 CF.sub.3 embedded image embedded image 1-122 CF.sub.3 embedded image embedded image 1-123 CF.sub.3 embedded image embedded image 1-124 CF.sub.3 embedded image embedded image 1-125 CF.sub.3 embedded image embedded image 1-126 CF.sub.3 embedded image embedded image 1-127 CF.sub.3 embedded image embedded image 1-128 CF.sub.3 embedded image embedded image 1-129 CF.sub.3 embedded image embedded image 1-130 CF.sub.3 embedded image embedded image 1-131 CF.sub.3 embedded image embedded image 1-132 CF.sub.3 embedded image embedded image 1-133 CF.sub.3 embedded image embedded image 1-134 CF.sub.3 embedded image embedded image 1-135 CF.sub.3 embedded image embedded image 1-136 CF.sub.3 embedded image embedded image 1-137 CF.sub.3 embedded image embedded image 1-138 CF.sub.3 embedded image embedded image 1-139 CF.sub.3 embedded image embedded image 1-140 CF.sub.3 embedded image embedded image 1-141 CF.sub.3 embedded image embedded image 1-142 CF.sub.3 embedded image embedded image 1-143 CF.sub.3 embedded image embedded image 1-144 CF.sub.3 embedded image embedded image 1-145 CF.sub.3 embedded image embedded image 1-146 CF.sub.3 embedded image embedded image 1-147 CF.sub.3 embedded image embedded image 1-148 CF.sub.3 embedded image embedded image 1-149 CF.sub.3 embedded image embedded image 1-150 CF.sub.3 embedded image embedded image 1-151 CF.sub.3 embedded image embedded image 1-152 CF.sub.3 embedded image embedded image 1-153 CF.sub.3 embedded image embedded image 1-154 CF.sub.3 embedded image embedded image 1-155 CF.sub.3 embedded image embedded image 1-156 CF.sub.3 embedded image embedded image 1-157 CF.sub.3 embedded image embedded image 1-158 CF.sub.3 embedded image embedded image 1-159 CF.sub.3 embedded image embedded image 1-160 CF.sub.3 embedded image embedded image 1-161 CF.sub.3 embedded image embedded image 1-162 CF.sub.3 embedded image embedded image 1-163 CF.sub.3 embedded image embedded image 1-164 CF.sub.3 embedded image embedded image 1-165 CF.sub.3 embedded image embedded image 1-166 CF.sub.3 embedded image embedded image 1-167 CF.sub.3 embedded image embedded image 1-168 CF.sub.3 embedded image embedded image 1-169 CF.sub.3 embedded image embedded image 1-170 CF.sub.3 embedded image embedded image 1-171 CF.sub.3 embedded image embedded image 1-172 CF.sub.3 embedded image embedded image 1-173 CF.sub.3 embedded image embedded image 1-174 CF.sub.3 embedded image embedded image 1-175 CF.sub.3 embedded image embedded image 1-176 CF.sub.3 embedded image embedded image 1-177 CF.sub.3 embedded image embedded image 1-178 CF.sub.3 embedded image embedded image 1-179 CF.sub.3 embedded image embedded image 1-180 CF.sub.3 embedded image embedded image 1-181 CF.sub.3 embedded image embedded image 1-182 CF.sub.3 embedded image embedded image 1-183 CF.sub.3 embedded image embedded image 1-184 CF.sub.3 embedded image embedded image 1-185 CF.sub.3 embedded image embedded image 1-186 CF.sub.3 embedded image embedded image 1-187 CF.sub.3 embedded image embedded image 1-188 CF.sub.3 embedded image embedded image 1-189 CF.sub.3 embedded image embedded image 1-190 CF.sub.3 embedded image embedded image 1-191 CF.sub.3 embedded image embedded image 1-192 CF.sub.3 embedded image embedded image 1-193 CF.sub.3 embedded image embedded image 1-194 CF.sub.3 embedded image embedded image 1-195 CF.sub.3 embedded image embedded image 1-196 CF.sub.3 embedded image embedded image 1-197 CF.sub.3 embedded image embedded image 1-198 CF.sub.3 embedded image embedded image 1-199 CF.sub.3 embedded image embedded image 1-200 CF.sub.3 embedded image embedded image 1-201 CF.sub.3 embedded image embedded image 1-202 CF.sub.3 OEt embedded image 1-203 CF.sub.3 embedded image embedded image 1-204 CF.sub.3 embedded image embedded image 1-205 CF.sub.3 embedded image embedded image 1-206 CF.sub.3 embedded image embedded image 1-207 CF.sub.3 embedded image embedded image 1-208 CF.sub.3 embedded image embedded image 1-209 CF.sub.3 embedded image embedded image 1-210 CF.sub.3 embedded image embedded image 1-211 CF.sub.3 embedded image embedded image 1-212 CF.sub.3 embedded image embedded image 1-213 CF.sub.3 embedded image embedded image 1-214 CF.sub.3 embedded image embedded image 1-215 CF.sub.3 embedded image embedded image 1-216 CF.sub.3 embedded image embedded image 1-217 CF.sub.3 embedded image embedded image 1-218 CH.sub.2F embedded image embedded image 1-219 CH.sub.2F embedded image embedded image 1-220 CH.sub.2F embedded image embedded image 1-221 CHF.sub.2 embedded image embedded image 1-222 CHF.sub.2 embedded image embedded image 1-223 CF.sub.2CF.sub.3 embedded image embedded image 1-224 CF.sub.2CF.sub.3 embedded image embedded image 1-225 CF.sub.2CF.sub.3 embedded image embedded image 1-226 CF.sub.3 embedded image embedded image 1-227 CF.sub.3 embedded image embedded image 1-228 CF.sub.3 embedded image embedded image 1-229 CF.sub.3 embedded image embedded image 1-230 CF.sub.3 embedded image embedded image 1-231 CF.sub.3 embedded image embedded image 1-232 CF.sub.3 embedded image embedded image 1-233 CF.sub.3 embedded image embedded image 1-234 CF.sub.3 embedded image embedded image 1-235 CF.sub.3 embedded image embedded image 1-236 CF.sub.3 embedded image embedded image 1-237 CF.sub.3 embedded image embedded image 1-238 CF.sub.3 embedded image embedded image 1-239 CF.sub.3 embedded image embedded image 1-240 CF.sub.3 embedded image embedded image 1-241 CF.sub.3 CN embedded image 1-242 CF.sub.3 embedded image embedded image 1-243 CF.sub.3 embedded image embedded image 1-244 CF.sub.3 embedded image embedded image 1-245 CF.sub.3 embedded image embedded image 1-246 CF.sub.3 embedded image embedded image 1-247 CF.sub.3 embedded image embedded image 1-248 CF.sub.3 embedded image embedded image 1-249 CF.sub.3 embedded image embedded image 1-250 CF.sub.3 embedded image embedded image 1-251 CF.sub.3 embedded image Me text missing or illegible when filed

    10. A method for preparing a pyridazinol compound or a derivative thereof according to claim 1, comprising: (1) subjecting a compound of Formula II and a compound of Formula III to Suzuki reaction to obtain a compound of Formula IV; (2) hydrolyzing the compound of Formula IV to obtain a compound of Formula I; wherein the reaction route is as follows: ##STR04236## or comprising: (a) hydrolyzing a compound of Formula II to give a compound of Formula V; (b) subjecting the compound of Formula V and a compound of Formula III to Suzuki reaction to obtain a compound of Formula I; wherein the reaction route is as follows: ##STR04237## wherein L is halogen, and other groups are as defined in claim 1.

    11. The method according to claim 10, wherein, each of the steps independently is carried out at a temperature in the range from 20 to 150° C.; wherein steps (1) and (b) are carried out in the presence of a catalyst, a base and a solvent, wherein the catalyst is Pd(dppf)Cl.sub.2CH.sub.2Cl.sub.2, Pd(dba).sub.2, Pd.sub.2(dba).sub.3, Pd(PPh.sub.3).sub.4, PdCl.sub.2, Pd(OAc).sub.2, Pd(dppf)Cl.sub.2, Pd(PPh.sub.3).sub.2Cl.sub.1, or Ni(dppf)Cl.sub.2, the base is one or more selected from Et.sub.3N, NaHCO.sub.3, KOAc, K.sub.2CO.sub.3, K.sub.3PO.sub.4, Na.sub.2CO.sub.3, CsF, Cs.sub.2CO.sub.3, t-BuONa, EtONa, KOH, and NaOH, and the solvent is THF/water, toluene/water, DMF/water, 1,4-dioxane/water, toluene/ethanol/water, acetonitrile/water, THF, toluene, 1,4-dioxane, acetonitrile, or DMF system; steps (2) and (a) are carried out in the presence of a base and a solvent or in the presence of a solution of boron tribromide, a solution of hydrobromic acid in acetic acid, a solution of hydrochloric acid in methanol or a solution of hydrochloric acid in ethyl acetate, wherein the base is selected from NaOH, KOH, potassium acetate, and sodium acetate, and the solvent is water or DMSO.

    12. A method for preparing a derivative of a pyridazinol compound according to claim 8, wherein, when the derivative is an ester or ether derivative, the reaction route is as follows: ##STR04238## wherein, Y.sub.1 is a halogen; when the derivative is an oxime or hydroxylamine derivative, the reaction route is as follows: ##STR04239## wherein, Y.sub.2 is a halogen; other groups are as defined in claim 8.

    13. The method according to claim 11, wherein the reactions for preparing the ester and ether derivatives and the second step for preparing the oxime and hydroxylamine derivatives are carried out in the presence of a base and a solvent, wherein the base is one or more selected from the group consisting of sodium hydroxide, potassium hydroxide, sodium carbonate, potassium carbonate, sodium hydrogen carbonate, cesium carbonate, triethylamine and diisopropylethylamine; the solvent is THF, 1,4-dioxane, toluene, 1,2-dichloroethane, ethyl acetate, acetonitrile, DMF, acetone, dichloromethane, or chloroform; the first step for preparing the oxime and hydroxylamine derivative is carried out in the presence of a halogenation reagent and a solvent, wherein the halogenation reagent is phenofluor/cesium fluoride or POCl.sub.3, and the solvent is one or more selected from the group consisting of toluene, 1,2-dichloroethane, and DMF; and the reaction temperature is in the range of 0 to 120° C.

    14. A herbicidal composition, comprising at least one compound chosen from the pyridazinol compound of Formula I and the derivative thereof according to claim 1.

    15-18. (canceled)

    19. A herbicidal composition, comprising at least one compound chosen from the derivative of the pyridazinol of Formula I-1 according to claim 8.

    20. The herbicidal composition according to claim 14, further comprising at least one additional herbicide.

    21. The herbicidal composition according to claim 19, further comprising at least one additional herbicide

    22. The herbicidal composition according to claim 20, wherein the at least one additional herbicide is selected from an HPPD inhibitor, a hormone herbicide, and a PDS inhibitor.

    23. A method for controlling a harmful plant, comprising applying a herbicidally effective amount of at least one compound selected from the pyridazinol compound and the derivative thereof according to claim 1 to the harmful plant or an area with the harmful plant.

    24. A method for controlling a harmful plant, comprising applying a herbicidally effective amount of at least one compound selected from the derivative of pyridazinol compound according to claim 8 to the harmful plant or an area with the harmful plant.

    25. A method for controlling a harmful plant in a useful crop, comprising applying a herbicidally effective amount of at least one compound selected from the pyridazinol compound and the derivative thereof according to claim 1 to the harmful plant, wherein the useful crop is selected from wheat, corn, rice, soybean, cotton, oilseed rape, millet and sorghum.

    26. A method for controlling a harmful plant in a useful crop, comprising applying a herbicidally effective amount of at least one compound selected from the derivative of pyridazinol compound according to claim 8 to the harmful plant, wherein the useful crop is selected from wheat, corn, rice, soybean, cotton, oilseed rape, millet and sorghum.

    27. The method according to claim 24, wherein the harmful plant is a monocotyledonous or dicotyledonous harmful plant, selected from Amaranthus retroflexus, Rorippa indica, Veronica polita, Chenopodiaceae, Echinochloa crus-galli, Setaria viridis, Galium aparine, Abutilon mill, Sisymbrium sophia and Galinsoga parviflora.

    28. The method according to claim 25, wherein the harmful plant is a monocotyledonous or dicotyledonous harmful plant, selected from Amaranthus retroflexus, Rorippa indica, Veronica polita, Chenopodiaceae, Echinochloa crus-galli, Setaria viridis, Galium aparine, Abutilon mill, Sisymbrium sophia and Galinsoga parviflora.

    Description

    SPECIFIC MODE FOR CARRYING OUT THE INVENTION

    [0188] The following embodiments are used to illustrate the present invention in detail and should not be taken as any limit to the present invention. The scope of the invention would be explained through the Claims.

    [0189] In view of economics, variety and biological activity of a compound, we preferably synthesized several compounds, part of which are listed in the following table 1-2. The structure and information of a certain compound are shown in Table 1-2. The compounds in Table 1-2 are listed for further explication of the present invention, other than any limit therefor. The subject of the present invention should not be interpreted by those skilled in the art as being limited to the following compounds.

    TABLE-US-00001 TABLE 1 Structure and .sup.1HNMR data of Compound I I [00076]embedded image No. X A .sup.1H NMR 1 CF.sub.3 [00077]embedded image (500 MHz, Chloroform-d) δ 7.55-7.47 (m, 2H), 7.41-7.27 (m, 3H), 7.06 (s, 1H), 5.58 (s, 1H). 2 CF.sub.3 [00078]embedded image (500 MHz, Chloroform-d) δ 7.46-7.40 (m, 1H), 7.39-7.30 (m, 2H), 7.32- 7.26 (m, 1H), 7.03 (s, 1H), 5.68 (s, 1H), 2.50 (s, 3H). 3 CF.sub.3 [00079]embedded image (500 MHz, Chloroform-d) δ 7.45-7.41 (m, 1H), 7.40-7.30 (m, 2H), 7.29- 7.23 (m, 1H), 7.06 (s, 1H), 5.58 (s, 1H), 2.50 (s, 3H). 4 CF.sub.3 [00080]embedded image (500 MHz, Chloroform-d) δ 7.44 (d, J = 7.5 Hz, 2H), 7.22 (d, J = 7.5 Hz, 2H), 7.06 (s, 1H), 5.57 (s, 1H), 2.33 (s, 3H). 5 CF.sub.3 [00081]embedded image (500 MHz, Chloroform-d) δ 7.47-7.44 (m, 1H), 7.43-7.34 (m, 2H), 7.34- 7.27 (m, 1H), 7.06 (s, 1H), 5.60 (s, 1H), 2.61 (q, J = 8.0 Hz, 2H), 1.21 (t, J = 8.0 Hz, 3H). 6 CF.sub.3 [00082]embedded image (500 MHz, Chloroform-d) δ 7.46 (d, J = 7.5 Hz, 2H), 7.11 (d, J = 7.5 Hz, 2H), 7.06 (s, 1H), 5.57 (s, 1H), 2.67 (q, J = 8.0 Hz, 2H), 1.19 (t, J = 8.0 Hz, 3H). 7 CF.sub.3 [00083]embedded image (500 MHz, Chloroform-d) δ 7.50-7.42 (m, 1H), 7.45-7.34 (m, 3H), 7.01 (s, 1H), 5.60 (s, 1H), 2.66 (q, J = 8.0, Hz, 2H), 1.20 (t, J = 8.0 Hz, 3H). 8 CF.sub.3 [00084]embedded image (500 MHz, Chloroform-d) δ 7.56 (d, J = 7.5 Hz, 2H), 7.43 (d, J = 7.5 Hz, 2H), 7.00 (s, 1H), 5.77 (s, 1H), 2.94 (hept, J = 8.0 Hz, 1H), 1.20 (d, J = 8.0 Hz, 6H). 9 CF.sub.3 [00085]embedded image (500 MHz, Chloroform-d) δ 7.55-7.50 (m, 1H), 7.45-7.33 (m, 3H), 7.06 (s, 1H), 5.61 (s, 1H), 2.90 (hept, J = 8.0 Hz, 1H), 1.24 (d, J = 8.0 Hz, 6H). 10 CF.sub.3 [00086]embedded image (500 MHz, Chloroform-d) δ 7.50-7.40 (m, 2H), 7.37-7.30 (m, 2H), 7.01 (s, 1H), 5.58 (s, 1H), 3.12 (hept, J = 8.0 Hz, 1H), 1.27 (d, J = 8.0 Hz, 6H). 11 CF.sub.3 [00087]embedded image (500 MHz, Chloroform-d) δ 7.56 (d, J = 7.5 Hz, 2H), 7.43 (d, J = 7.5 Hz, 2H), 7.00 (s, 1H), 5.77 (s, 1H), 2.61-2.46 (m, 1H), 1.80-1.61 (m, 2H), 1.16 (d, J = 7.0 Hz, 3H), 0.76 (t, J = 8.0 Hz, 3H). 12 CF.sub.3 [00088]embedded image (500 MHz, Chloroform-d) δ 7.57-7.39 (m, 2H), 7.42-7.33 (m, 2H), 7.06 (s, 1H), 5.58 (s, 1H), 2.65-2.49 (m, 1H), 1.84-1.65 (m, 2H), 1.18 (d, J = 7.0 Hz, 3H), 0.79 (t, J = 8.0 Hz, 3H). 13 CF.sub.3 [00089]embedded image (500 MHz, Chloroform-d) δ 7.50-7.35 (m, 4H), 7.04 (s, 1H), 5.67 (s, 1H), 2.79-2.68 (m, 1H), 1.94-1.75 (m, 2H), 1.28 (d, J = 7.0 Hz, 3H), 0.83 (t, J = 8.0 Hz, 3H). 14 CF.sub.3 [00090]embedded image (500 MHz, Chloroform-d) δ 7.46 (d, J = 7.5 Hz, 2H), 7.12 (d, J = 7.5 Hz, 2H), 7.06 (s, 1H), 5.56 (s, 1H), 2.59 (t, J = 7.5 Hz, 2H), 1.56-1.32 (m, 4H), 0.89 (t, J = 8.0 Hz, 3H). 15 CF.sub.3 [00091]embedded image (500 MHz, Chloroform-d) δ 7.47-7.33 (m, 3H), 7.34-7.28 (m, 1H), 7.06 (s, 1H), 5.59 (s, 1H), 2.61 (t, J = 7.5 Hz, 2H), 1.59-1.37 (m, 4H), 0.95 (t, J = 8.0 Hz, 3H). 16 CF.sub.3 [00092]embedded image (500 MHz, Chloroform-d) δ 7.49-7.37 (m, 4H), 7.01 (s, 1H), 5.62 (s, 1H), 2.58 (t, J = 7.5 Hz, 2H), 1.53-1.33 (m, 4H), 0.85 (t, J = 8.0 Hz, 3H). 17 CF.sub.3 [00093]embedded image (500 MHz, Chloroform-d) δ 7.54 (d, J = 7.5 Hz, 2H), 7.43 (d, J = 7.5 Hz, 2H), 7.06 (s, 1H), 5.56 (s, 1H), 1.28 (s, 9H). 18 CF.sub.3 [00094]embedded image (500 MHz, Chloroform-d) δ 7.60 (dd, J = 2.0, 1.5 Hz, 1H), 7.53-7.45 (m, 1H), 7.39-7.30 (m, 2H), 7.06 (s, 1H), 5.60 (s, 1H), 1.33 (s, 9H). 19 CF.sub.3 [00095]embedded image (500 MHz, Chloroform-d) δ 7.47 (dd, J = 7.0, 2.5 Hz, 1H), 7.40-7.31 (m, 2H), 7.29 (dd, J = 6.5, 3.0 Hz, 1H), 7.03 (s, 1H), 5.64 (s, 1H), 1.24 (s, 9H). 20 CF.sub.3 [00096]embedded image (500 MHz, Chloroform-d) δ 7.58-7.52 (m, 2H), 7.45-7.38 (m, 2H), 7.01 (s, 1H), 6.40-6.33 (m, 1H), 6.15-6.01 (m, 1H), 5.78 (s, 1H), 1.72 (d, J = 6.5 Hz, 3H). 21 CF.sub.3 [00097]embedded image (500 MHz, Chloroform-d) δ 7.82-7.42 (m, 4H), 7.02 (s, 1H), 6.91-6.70 (m, 1H), 5.92 (s, 1H), 5.70-5.49 (m, 2H). 22 CF.sub.3 [00098]embedded image (500 MHz, Chloroform-d) δ 7.73 (d, J = 7.5 Hz, 2H), 7.67 (d, J = 7.5 Hz, 2H), 7.05 (s, 1H), 5.51 (s, 1H), 1.86 (s, 3H). 23 CF.sub.3 [00099]embedded image (500 MHz, Chloroform-d) δ 7.79 (dd, J = 2.0, 1.5 Hz, 1H), 7.57-7.35 (m, 3H), 7.06 (s, 1H), 5.53 (s, 1H), 3.14 (s, 1H). 24 CF.sub.3 [00100]embedded image (500 MHz, Chloroform-d) δ 7.47 (d, J = 7.5 Hz, 2H), 7.34 (d, J = 7.5 Hz, 2H), 7.06 (s, 1H), 5.53 (s, 1H), 1.93-1.84 (m, 1H), 1.20-1.11 (m, 2H), 0.92- 0.83 (m, 2H). 25 CF.sub.3 [00101]embedded image (500 MHz, Chloroform-d) δ 7.56 (d, J = 7.5 Hz, 2H), 7.44 (d, J = 7.5 Hz, 2H), 7.00 (s, 1H), 5.76 (s, 1H), 2.60-2.51 (m, 1H), 1.94-1.81 (m, 8H), 1.81- 1.71 (m, 2H). 26 CF.sub.3 [00102]embedded image (500 MHz, Chloroform-d) δ 7.60-7.51 (m, 1H), 7.39-7.16 m, 3H), 7.09 (s, 1H), 5.81 (s, 1H). 27 CF.sub.3 [00103]embedded image (500 MHz, Chloroform-d) δ 7.82-7.68 (m, 1H), 7.73 (dd, J = 2.0, 1.5 Hz, 1H), 7.42-7.37 (m, 2H), 7.07 (s, 1H), 5.51 (s, 1H). 28 CF.sub.3 [00104]embedded image (500 MHz, Chloroform-d) δ 7.70 (d, J = 7.5 Hz, 2H), 7.57 (d, J = 7.5 Hz, 2H), 7.00 (s, 1H), 5.78 (s, 1H). 29 CF.sub.3 [00105]embedded image (500 MHz, Chloroform-d) δ 7.99 (dd, J = 2.0, 1.5 Hz, 1H), 7.83-7.47 (m, 2H), 7.16-7.03 (m, 1H), 7.06 (s, 1H), 5.49 (s, 1H). 30 CF.sub.3 [00106]embedded image (500 MHz, Chloroform-d) δ 7.49-7.39 (m, 3H), 7.29-7.17 (m, 1H), 7.04 (s, 1H), 5.94 (s, 1H). 31 CF.sub.3 [00107]embedded image (500 MHz, Chloroform-d) δ 7.84 (dd, J = 2.0, 1.5 Hz, 1H), 7.64-7.31 (m, 1H), 7.01 (s, 1H), 5.80 (s, 1H). 32 CF.sub.3 [00108]embedded image (500 MHz, Chloroform-d) δ 7.44-7.16 (m, 2H), 7.11-6.95 (m, 2H), 7.07 (s, 2H), 5.48 (s, 1H). 33 CF.sub.3 [00109]embedded image (500 MHz, Chloroform-d) δ 7.89 (d, J = 7.5 Hz, 2H), 7.34 (d, J = 7.5 Hz, 2H), 7.06 (s, 1H), 5.47 (s, 1H). 34 CF.sub.3 [00110]embedded image (500 MHz, Chloroform-d) δ 7.45-7.38 (m, 2H), 7.30-7.14 (m, 1H), 7.01 (s, 1H), 5.68 (s, 1H). 35 CF.sub.3 [00111]embedded image (500 MHz, Chloroform-d) δ 7.41-7.35 (m, 2H), 7.02 (s, 1H), 6.95-6.76 (m, 1H), 5.82 (s, 1H). 36 CF.sub.3 [00112]embedded image (500 MHz, Chloroform-d) δ 7.71-7.57 (m, 1H), 7.22-7.06 (m, 2H), 7.11 (s, 1H), 5.20 (s, 1H). 37 CF.sub.3 [00113]embedded image (500 MHz, Chloroform-d) δ 7.52-7.44 (m, 3H), 7.04 (s, 1H), 5.94 (s, 1H). 38 CF.sub.3 [00114]embedded image (500 MHz, Chloroform-d) δ 7.69 (d, J = 2.0 Hz, 1H), 7.35 (dd, J = 7.5, 2.0 Hz, 1H), 7.26 (d, J = 7.5 Hz, 1H), 7.01 (s, 1H), 5.79 (s, 1H). 39 CF.sub.3 [00115]embedded image (500 MHz, Chloroform-d) δ 7.53 (d, J = 2.0 Hz, 1H), 7.48 (d, J = 7.5 Hz, 1H), 7.33 (dd, J = 7.5, 2.0 Hz, 1H), 7.04 (s, 1H), 5.93 (s, 1H). 40 CF.sub.3 [00116]embedded image (500 MHz, Chloroform-d) δ 7.71-7.45 (m, 3H), 7.01 (s, 1H), 5.81 (s, 1H). 41 CF.sub.3 [00117]embedded image (500 MHz, Chloroform-d) δ 7.48-7.41 (m, 3H), 7.03 (s, 1H), 5.58 (s, 1H). 42 CF.sub.3 [00118]embedded image (500 MHz, Chloroform-d) δ 7.70 (dd, J = 7.5, 2.0 Hz, 1H), 7.36 (dd, J = 8.0, 2.0 Hz, 1H), 7.28 (dd, J = 8.0, 7.5 Hz, 1H), 7.04 (s, 1H), 5.92 (s, 1H). 43 CF.sub.3 [00119]embedded image (500 MHz, Chloroform-d) δ 7.54-7.40 (m, 2H), 7.15-7.09 (m, 1H), 7.11 (s, 1H), 5.61 (s, 1H). 44 CF.sub.3 [00120]embedded image (500 MHz, Chloroform-d) δ 7.48-7.40 (m, 2H), 7.06-6.99 (m, 2H), 5.92 (s, 1H). 45 CF.sub.3 [00121]embedded image (500 MHz, Chloroform-d) δ 7.49-7.43 (m, 2H), 7.14-7.02 (m, 1H), 7.02 (s, 1H), 5.47 (s, 1H). 46 CF.sub.3 [00122]embedded image (500 MHz, Chloroform-d) δ 7.59-7.49 (m, 1H), 7.36-7.21 (m, 1H), 7.02 (s, 1H), 5.82 (s, 1H). 47 CF.sub.3 [00123]embedded image (500 MHz, Chloroform-d) δ 7.41-7.18 (m, 3H), 7.04 (s, 1H), 5.51 (s, 1H). 48 CF.sub.3 [00124]embedded image (500 MHz, Chloroform-d) δ 7.57-7.41 (m, 2H), 7.12 (s, 1H), 7.07-6.93 (m, 1H), 5.48 (s, 1H). 49 CF.sub.3 [00125]embedded image (500 MHz, Chloroform-d) δ 7.62-7.53 (m, 2H), 7.40-7.22 (m, 1H), 7.01 (s, 1H), 5.81 (s, 1H). 50 CF.sub.3 [00126]embedded image (500 MHz, Chloroform-d) δ 7.83-7.58 (m, 2H), 7.25-7.11 (m, 1H), 7.02 (s, 1H), 5.52 (s, 1H). 51 CF.sub.3 [00127]embedded image (500 MHz, Chloroform-d) δ 7.59-7.46 (m, 2H), 7.41-7.35 (m, 1H), 7.01 (s, 1H), 5.68 (s, 1H). 52 CF.sub.3 [00128]embedded image (500 MHz, Chloroform-d) δ 7.00 (s, 1H), 6.75-6.52 (m, 2H), 5.64 (s, 1H). 53 CF.sub.3 [00129]embedded image (500 MHz, Chloroform-d) δ 7.28-7.20 (m, 2H), 7.02 (s, 1H), 5.84 (s, 1H). 54 CF.sub.3 [00130]embedded image (500 MHz, Chloroform-d) δ 7.17-7.03 (m, 3H), 6.98-6.77 (m, 1H), 4.92 (s, 1H). 55 CF.sub.3 [00131]embedded image (500 MHz, Chloroform-d) δ 7.03 (s, 1H), 5.57 (s, 1H). 56 CF.sub.3 [00132]embedded image (500 MHz, Chloroform-d) δ 7.34 (dd, J = 9.0, 1.5 Hz, 1H), 7.24-7.07 (m, 1H), 7.17 (dd, J = 7.5, 2.5 Hz, 1H), 7.07 (s, 1H), 5.45 (s, 1H), 2.31 (s, 3H). 57 CF.sub.3 [00133]embedded image (500 MHz, Chloroform-d) δ 7.48-7.42 (m, 1H), 7.25-7.10 (m, 2H), 7.02 (s, 1H), 5.46 (s, 1H), 2.50 (s, 3H). 58 CF.sub.3 [00134]embedded image (500 MHz, Chloroform-d) δ 7.22-7.08 (m, 3H), 7.01 (s, 1H), 5.66 (s, 1H), 2.44 (s, 3H). 59 CF.sub.3 [00135]embedded image (500 MHz, Chloroform-d) δ 7.55-7.40 (m, 1H), 7.09 (s, 1H), 7.03-6.95 (m, 2H), 5.79 (s, 1H), 2.35 (s, 3H). 60 CF.sub.3 [00136]embedded image (500 MHz, Chloroform-d) δ 8.74-8.55 (m, 1H), 7.44-7.17 (m, 2H), 7.09 (s, 1H), 5.89 (s, 1H), 3.90 (s, 3H). 61 CF.sub.3 [00137]embedded image (500 MHz, Chloroform-d) δ 8.54 (dd, J = 5.5, 2.0 Hz, 1H), 8.27-8.03 (m, 1H), 7.44 (dd, J = 10.5, 7.5 Hz, 1H), 7.13 (s, 1H), 5.37 (s, 1H). 62 CF.sub.3 [00138]embedded image (500 MHz, Chloroform-d) δ 7.46-7.22 (m, 1H), 7.09-6.96 (m, 2H), 6.92- 6.76 (m, 1H), 5.58 (s, 1H), 3.90 (s, 3H). 63 CF.sub.3 [00139]embedded image (500 MHz, Chloroform-d) δ 7.74-7.64 (m, 2H), 7.39-7.22 (m, 2H), 6.51 (s, 1H). 64 CF.sub.3 [00140]embedded image (500 MHz, Chloroform-d) δ 7.71-7.64 (m, 2H), 7.61-7.46 (m, 1H), 7.11 (s, 1H), 5.86 (s, 1H), 5.60 (s, 1H). 65 CF.sub.3 [00141]embedded image (500 MHz, Chloroform-d) δ 7.93-7.78 (m, 1H), 7.60-7.39 (m, 2H), 7.07 (s, 1H), 5.84 (s, 1H), 5.41 (s, 1H). 66 CF.sub.3 [00142]embedded image (500 MHz, Chloroform-d) δ 8.27 (dd, J = 5.5, 2.0 Hz, 1H), 7.76-7.61 (m, 1H), 7.42 (dd, J = 10.5, 7.5 Hz, 1H), 7.06 (s, 1H), 5.47 (s, 1H). 67 CF.sub.3 [00143]embedded image (500 MHz, Chloroform-d) δ 7.73-7.56 (m, 1H), 7.51 (dd, J = 11.0, 2.0 Hz, 1H), 7.31 (s, 1H), 7.25-7.10 (m, 1H), 6.57 (s, 1H). 68 CF.sub.3 [00144]embedded image (500 MHz, Chloroform-d) δ 7.30-7.22 (m, 1H), 7.11-7.00 (m, 3H), 5.74 (s, 1H), 3.90 (s, 3H). 69 CF.sub.3 [00145]embedded image (500 MHz, Chloroform-d) δ 8.42 (d, J = 2.0 Hz, 1H), 8.19 (dd, J = 7.5, 2.0 Hz, 1H), 7.76 (d, J = 7.5 Hz, 1H), 7.06 (s, 1H), 5.75 (s, 1H). 70 CF.sub.3 [00146]embedded image (500 MHz, Chloroform-d) δ 7.54 (d, J = 7.5 Hz, 1H), 7.15 (d, J = 2.0 Hz, 1H), 7.00 (s, 1H), 6.90 (dd, J = 7.5, 2.0 Hz, 1H), 5.62 (s, 1H), 3.87 (s, 3H). 71 CF.sub.3 [00147]embedded image (500 MHz, Chloroform-d) δ 7.39-7.32 (m, 2H), 7.21 (dd, J = 7.5, 2.0 Hz, 1H), 7.04 (s, 1H), 5.66 (s, 1H), 2.34 (s, 3H). 72 CF.sub.3 [00148]embedded image (500 MHz, Chloroform-d) δ 7.48-7.42 (m, 2H), 7.25 (dd, J = 7.5, 2.0 Hz, 1H), 7.07 (s, 1H), 5.47 (s, 1H), 2.32 (s, 3H). 73 CF.sub.3 [00149]embedded image (500 MHz, Chloroform-d) δ 7.60 (d, J = 7.5 Hz, 1H), 7.07 (d, J = 2.0 Hz, 1H), 7.00 (s, 1H), 6.84 (dd, J = 7.5, 2.0 Hz, 1H), 5.63 (s, 1H), 3.81 (s, 3H). 74 CF.sub.3 [00150]embedded image (500 MHz, Chloroform-d) δ 7.60 (dd, J = 2.0, 1.5 Hz, 1H), 7.38-7.28 (m, 2H), 7.07 (s, 1H), 5.47 (s, 1H), 2.34 (s, 3H). 75 CF.sub.3 [00151]embedded image (500 MHz, Chloroform-d) δ 7.50 (d, J = 2.0 Hz, 1H), 7.29 (dd, J = 7.5, 2.0 Hz, 1H), 7.23 (d, J = 7.5 Hz, 1H), 7.07 (s, 1H), 5.48 (s, 1H), 2.28 (s, 3H). 76 CF.sub.3 [00152]embedded image (500 MHz, Chloroform-d) δ 7.38 (d, J = 7.5 Hz, 1H), 7.00 (s, 1H), 6.88-6.80 (m, 2H), 5.61 (s, 1H), 3.71 (s, 3H), 2.34 (s, 3H). 77 CF.sub.3 [00153]embedded image (500 MHz, Chloroform-d) δ 7.37 (d, J = 7.5 Hz, 1H), 7.10-7.02 (m, 2H), 7.04 (s, 1H), 5.68 (s, 1H), 2.36-2.29 (m, 6H). 78 CF.sub.3 [00154]embedded image (500 MHz, Chloroform-d) δ 7.33-7.16 (m, 3H), 7.03 (s, 1H), 5.60 (s, 1H), 2.30 (s, 6H). 79 CF.sub.3 [00155]embedded image (500 MHz, Chloroform-d) δ 7.52-7.38 (m, 3H), 7.01 (s, 1H), 5.78 (s, 1H), 1.33 (s, 6H). 80 CF.sub.3 [00156]embedded image (500 MHz, Chloroform-d) δ 8.97 (s, 1H), 7.09 (s, 1H), 7.03-6.95 (m, 2H), 3.82 (s, 3H), 3.76 (s, 3H), 3.72 (s, 3H). 81 CF.sub.3 [00157]embedded image (500 MHz, Chloroform-d) δ 7.02-6.91 (m, 3H), 5.63 (s, 1H), 4.34 (q, J = 8.0 Hz, 2H), 1.61 (t, J = 8.0 Hz, 3H). 82 CF.sub.3 [00158]embedded image (500 MHz, Chloroform-d) δ 7.25 (d, J = 7.5 Hz, 1H), 7.20-7.13 (m, 1H), 7.00 (s, 1H), 5.60 (s, 1H), 2.30 (s, 3H). 83 CF.sub.3 [00159]embedded image (500 MHz, Chloroform-d) δ 7.57 (d, J = 7.5 Hz, 2H), 7.09 (d, J = 7.5 Hz, 2H), 7.00 (s, 1H), 5.76 (s, 1H), 3.99 (t, J = 7.5 Hz, 2H), 1.75-1.61 (m, 2H), 1.14 (t, J = 8.0 Hz, 3H). 84 CF.sub.3 [00160]embedded image (500 MHz, Chloroform-d) δ 7.57-7.50 (m, 2H), 7.09-7.03 (m, 2H), 7.00 (s, 1H), 5.76 (s, 1H). 85 CF.sub.3 [00161]embedded image (500 MHz, Chloroform-d) δ 7.47-7.41 (m, 2H), 7.41-7.35 (m, 2H), 7.06 (s, 1H). 86 CF.sub.3 [00162]embedded image (500 MHz, Chloroform-d) δ 7.19 (dd, J = 8.0, 7.5 Hz, 1H), 7.13-7.02 (m, 3H), 6.93-6.78 (m, 1H). 87 CF.sub.3 [00163]embedded image (500 MHz, Chloroform-d) δ 7.38 (d, J = 7.5 Hz, 2H), 7.06 (s, 1H), 6.84 (d, J = 7.5 Hz, 2H), 5.57 (s, 1H), 4.92 (s, 1H). 88 CF.sub.3 [00164]embedded image (500 MHz, Chloroform-d) δ 7.15-7.01 (m, 2H), 7.03-6.97 (m, 1H), 6.72- 6.57 (m, 2H), 5.77 (s, 1H), 4.14 (s, 2H). 89 CF.sub.3 [00165]embedded image (500 MHz, Chloroform-d) δ 8.28 (d, J = 7.5 Hz, 2H), 7.87 (d, J = 7.5 Hz, 2H), 7.02 (s, 1H), 5.84 (s, 1H). 90 CF.sub.3 [00166]embedded image (500 MHz, Chloroform-d) δ 8.28-8.22 (m, 2H), 7.87-7.80 (m, 2H), 7.02 (s, 1H), 5.84 (s, 1H). 91 CF.sub.3 [00167]embedded image (500 MHz, Chloroform-d) δ 8.02 (d, J = 7.5 Hz, 2H), 7.77 (d, J = 7.5 Hz, 2H), 7.02 (s, 1H), 5.82 (s, 1H). 92 CF.sub.3 [00168]embedded image (500 MHz, Chloroform-d) δ 7.99-7.91 (m, 2H), 7.75-7.60 (m, 2H), 7.07 (s, 1H), 5.52 (s, 1H). 93 CF.sub.3 [00169]embedded image (500 MHz, Chloroform-d) δ 7.48 (d, J = 7.5 Hz, 2H), 7.06 (s, 1H), 6.80 (d, J = 7.5 Hz, 2H), 5.56 (s, 1H), 3.80 (s, 3H). 94 CF.sub.3 [00170]embedded image (500 MHz, Chloroform-d) δ 7.66-7.40 (m, 4H), 7.08 (s, 1H), 5.87 (s, 1H), 3.90 (s, 3H). 95 CF.sub.3 [00171]embedded image (500 MHz, Chloroform-d) δ 7.68 (dd, J = 2.0, 1.5 Hz, 1H), 7.46-7.35 (m, 3H), 7.01 (s, 1H), 5.80 (s, 1H), 2.50 (s, 3H). 96 CF.sub.3 [00172]embedded image (500 MHz, Chloroform-d) δ 7.61 (d, J = 7.5 Hz, 2H), 7.44 (d, J = 7.5 Hz, 2H), 7.01 (s, 1H), 5.77 (s, 1H), 3.25 (hept, J = 7.0 Hz, 1H), 1.40 (d, J = 7.0 Hz, 6H). 97 CF.sub.3 [00173]embedded image (500 MHz, Chloroform-d) δ 7.59 (d, J = 7.5 Hz, 2H), 7.05 (s, 1H), 6.70 (d, J = 7.5 Hz, 2H), 5.56 (s, 1H), 3.02 (s, 6H). 98 CF.sub.3 [00174]embedded image (500 MHz, Chloroform-d) δ 7.49 (d, J = 7.5 Hz, 2H), 7.16 (d, J = 7.5 Hz, 2H), 7.07 (s, 1H), 5.53 (s, 1H), 4.47-4.37 (m, 2H), 2.76-2.69 (m, 2H). 99 CF.sub.3 [00175]embedded image (500 MHz, Chloroform-d) δ 7.33-7.25 (m, 2H), 7.20-6.96 (m, 2H), 5.61 (s, 1H), 4.46 (q, J = 9.5 Hz, 2H). 100 CF.sub.3 [00176]embedded image 101 CF.sub.3 [00177]embedded image (500 MHz, Chloroform-d) δ 7.35-7.23 (m, 3H), 7.02-6.94 (m, 2H), 5.76 (s, 1H), 4.41 (hept, J = 7.0 Hz, 1H), 1.29 (d, J = 7.0 Hz, 6H). 102 CF.sub.3 [00178]embedded image (500 MHz, Chloroform-d) δ 7.53 (d, J = 7.0 Hz, 2H), 7.41 (d, J = 7.0 Hz, 2H), 7.06 (s, 1H), 5.54 (s, 1H), 2.83 (q, J = 8.0 Hz, 2H), 1.38 (t, J = 8.0 Hz, 3H). 103 CF.sub.3 [00179]embedded image (500 MHz, Chloroform-d) δ 7.19 (dd, J = 7.5, 7.0 Hz, 1H), 7.06 (s, 1H), 6.92- 6.70 (m, 2H), 6.63 (dd, J = 2.0, 1.5 Hz, 1H), 5.62 (s, 1H), 4.09 (s, 1H), 3.36 (q, J = 8.0 Hz, 2H), 1.23 (t, J = 8.0 Hz, 3H). 104 CF.sub.3 [00180]embedded image (500 MHz, Chloroform-d) δ 7.49 (d, J = 7.0 Hz, 2H), 7.19-7.03 (m, 3H), 5.47 (s, 1H), 5.14-4.91 (m, 1H), 4.04-3.91 (m, 2H). 105 CF.sub.3 [00181]embedded image (500 MHz, Chloroform-d) δ 8.85 (s, 1H), 7.58 (dd, J = 7.5, 2.0 Hz, 1H), 7.40-7.18 (m, 2H), 7.11 (dd, J = 7.0, 2.0 Hz, 1H), 7.08 (s, 1H), 4.38 (q, J = 8.0 Hz, 2H), 1.45 (t, J = 8.0 Hz, 3H). 106 CF.sub.3 [00182]embedded image (500 MHz, Chloroform-d) δ 7.96 (d, J = 8.0 Hz, 2H), 7.73 (s, 1H), 7.69 (d, J = 8.0 Hz, 2H), 7.01 (s, 1H), 5.78 (s, 1H), 2.10 (s, 3H). 107 CF.sub.3 [00183]embedded image (500 MHz, Chloroform-d) δ 8.08 (d, J = 7.0 Hz, 2H), 7.61 (d, J = 7.0 Hz, 2H), 7.07 (s, 1H), 5.49 (s, 1H), 3.95 (s, 3H). 108 CF.sub.3 [00184]embedded image (500 MHz, Chloroform-d) δ 7.51 (d, J = 7.5 Hz, 2H), 7.06 (d, J = 7.5 Hz, 2H), 7.00 (s, 1H), 5.61 (s, 1H), 2.29 (s, 3H). 109 CF.sub.3 [00185]embedded image (500 MHz, Chloroform-d) δ 7.71 (dd, J = 2.0, 1.5 Hz, 1H), 7.62-7.55 (m, 2H), 7.43 (dd, J = 8.0, 7.5 Hz, 1H), 7.01 (s, 1H), 5.77 (s, 1H), 4.47 (s, 2H), 3.58 (q, J = 8.0 Hz, 2H), 1.18 (t, J = 8.0 Hz, 3H). 110 CF.sub.3 [00186]embedded image (500 MHz, Chloroform-d) δ 7.84 (dd, J = 2.5, 1.5 Hz, 1H), 7.47-7.38 (m, 3H), 7.01 (s, 1H), 5.84 (s, 1H), 5.69 (s, 2H), 3.52 (s, 2H). 111 CF.sub.3 [00187]embedded image (500 MHz, Chloroform-d) δ 7.49 (d, J = 7.5 Hz, 2H), 7.39 (d, J = 7.5 Hz, 2H), 7.06 (s, 1H), 5.54 (s, 1H), 3.48-3.33 (m, 1H), 2.43-2.29 (m, 1H), 1.51- 1.33 (m, 1H). 112 CF.sub.3 [00188]embedded image (500 MHz, Chloroform-d) δ 7.58 (d, J = 7.5 Hz, 2H), 7.51 (d, J = 7.5 Hz, 2H), 7.06 (s, 1H), 5.53 (s, 1H), 3.71 (s, 2H), 2.47 (q, J = 8.0 Hz, 2H), 1.16 (t, J = 8.0 Hz, 3H). 113 CF.sub.3 [00189]embedded image (500 MHz, Chloroform-d) δ 7.99 (d, J = 7.5 Hz, 2H), 7.61 (d, J = 7.5 Hz, 2H), 7.07 (s, 1H), 5.58 (s, 1H), 2.51 (s, 3H). 114 CF.sub.3 [00190]embedded image (500 MHz, Chloroform-d) δ 7.98 (d, J = 7.5 Hz, 2H), 7.85 (d, J = 7.5 Hz, 2H), 7.07 (s, 1H), 5.53 (s, 1H), 3.30 (s, 3H). 115 CF.sub.3 [00191]embedded image (500 MHz, Chloroform-d) δ 8.19 (dd, J = 2.0, 1.5 Hz, 1H), 8.04-7.80 (m, 2H), 7.66 (dd, J = 8.0, 7.5 Hz, 1H), 7.07 (s, 1H), 5.43 (s, 1H), 3.25 (s, 3H). 116 CF.sub.3 [00192]embedded image (500 MHz, Chloroform-d) δ 7.95 (d, J = 7.5 Hz, 2H), 7.71 (d, J = 7.5 Hz, 2H), 7.07 (s, 1H), 5.53 (s, 1H), 4.07 (q, J = 6.5 Hz, 4H), 1.17 (t, J = 6.5 Hz, 6H). 117 CF.sub.3 [00193]embedded image (500 MHz, Chloroform-d) δ 7.86-7.79 (m, 4H), 7.62-7.56 (m, 2H), 7.37- 7.29 (m, 3H), 7.07 (s, 1H), 5.62 (s, 1H). 118 CF.sub.3 [00194]embedded image (500 MHz, Chloroform-d) δ 8.09-7.96 (m, 3H), 7.62-7.56 (m, 4H), 7.44- 7.28 (m, 4H), 7.37-7.29 (m, 2H), 7.02 (s, 1H), 5.84 (s, 1H). 119 CF.sub.3 [00195]embedded image (500 MHz, Chloroform-d) δ 7.49-7.38 (m, 3H), 7.28 (dd, J = 2.0, 1.5 Hz, 1H), 7.02 (s, 1H), 6.56 (s, 1H), 5.87 (s, 1H), 3.67 (s, 3H). 120 CF.sub.3 [00196]embedded image (500 MHz, Chloroform-d) δ 7.29 (s, 2H), 7.00 (s, 1H), 6.00-5.88 (m, 1H), 5.77 (s, 1H), 5.30-5.21 (m, 1H), 5.15- 5.04 (m, 1H), 4.05-3.99 (m, 2H), 3.29 (q, J = 8.0 Hz, 2H), 2.27 (s, 6H), 1.09 (t, J = 8.0 Hz, 3H). 121 CF.sub.3 [00197]embedded image (500 MHz, Chloroform-d) δ 7.23 (dd, J = 7.5, 7.0 Hz, 1H), 7.17-7.11 (m, 1H), 7.07 (s, 1H), 6.92-6.81 (m, 1H), 6.69 (dd, J = 2.0, 1.5 Hz, 1H), 5.54 (s, 1H), 5.18 (s, 2H), 4.22 (s, 1H), 2.97 (s, 3H). 122 CF.sub.3 [00198]embedded image (500 MHz, Chloroform-d) δ 7.56-7.37 (m, 3H), 7.20 (dd, J = 2.0, 1.5 Hz, 1H), 7.02 (s, 1H), 5.84 (s, 1H), 5.46 (s, 2H), 3.68 (s, 2H), 3.20 (s, 3H). 123 CF.sub.3 [00199]embedded image (500 MHz, Chloroform-d) δ 7.42-7.14 (m, 4H), 7.06 (s, 1H), 6.56 (s, 1H), 5.97 (s, 1H), 4.15 (q, J = 8.0 Hz, 2H), 1.26 (t, J = 8.1 Hz, 3H). 124 CF.sub.3 [00200]embedded image (500 MHz, Chloroform-d) δ 7.17 (dd, J = 7.5, 7.0 Hz, 1H), 7.05 (s, 1H), 6.94- 6.88 (m, 2H), 6.63 (dd, J = 2.0, 1.5 Hz, 1H), 5.61 (s, 1H), 4.09 (s, 2H), 3.00 (s, 3H), 2.76 (s, 1H). 125 CF.sub.3 [00201]embedded image (500 MHz, Chloroform-d) δ 7.36-7.29 (m, 1H), 7.25-7.17 (m, 5H), 7.10- 7.03 (m, 1H), 7.00 (s, 1H), 6.87-6.80 (m, 2H), 5.74 (s, 1H), 3.35 (s, 3H). 126 CF.sub.3 [00202]embedded image (500 MHz, Chloroform-d) δ 7.40-7.23 (m, 3H), 7.05 (s, 1H), 6.52 (dd, J = 2.0, 1.5 Hz, 1H), 6.39 (s, 1H), 6.01 (s, 1H), 2.99 (s, 3H). 127 CF.sub.3 [00203]embedded image (500 MHz, Chloroform-d) δ 7.20-7.21 (m, 3H), 7.08 (s, 1H), 6.55 (dd, J = 2.0, 1.5 Hz, 1H), 6.38 (s, 1H), 6.05 (s, 1H), 3.45 (q, J = 8.0 Hz, 2H), 1.59 (t, J = 8.0 Hz, 3H). 128 CF.sub.3 [00204]embedded image (500 MHz, Chloroform-d) δ 7.59 (d, J = 7.5 Hz, 2H), 7.27 (d, J = 7.5 Hz, 2H), 7.00 (s, 1H), 5.78 (s, 1H). 129 CF.sub.3 [00205]embedded image (500 MHz, Chloroform-d) δ 7.38 (dd, J = 7.5, 7.0 Hz, 1H), 7.13 (dd, J = 7.5, 2.0 Hz, 1H), 7.09 (s, 1H), 7.07 (dd, J = 7.0, 2.0 Hz, 1H), 6.02 (s, 1H), 5.77 (s, 2H), 3.13 (s, 3H), 2.33 (s, 3H). 130 CF.sub.3 [00206]embedded image (500 MHz, Chloroform-d) δ 7.42-7.37 (m, 1H), 7.33-7.24 (m, 2H), 7.01 (s, 1H), 7.04-6.97 (m, 1H), 5.81 (s, 1H), 4.71 (s, 2H). 131 CF.sub.3 [00207]embedded image (500 MHz, Chloroform-d) δ 7.41 (dd, J = 2.0, 1.5 Hz, 1H), 7.11 (dd, J = 2.5, 2.0 Hz, 1H), 7.06 (d, J = 2.5, 1.5 Hz, 1H), 7.00 (s, 1H), 5.48 (s, 1H), 4.68 (s, 2H), 3.00 (s, 1H). 132 CF.sub.3 [00208]embedded image (500 MHz, Chloroform-d) δ 7.33-7.23 (m, 3H), 7.03-6.96 (m, 2H), 5.77 (s, 1H), 3.92 (d, J = 6.5 Hz, 2H), 1.84- 1.73 (m, 2H), 1.77-1.61 (m, 3H), 1.65- 1.51 (m, 2H), 1.25-1.14 (m, 2H). 133 CF.sub.3 [00209]embedded image (500 MHz, Chloroform-d) δ 7.07-6.99 (m, 4H), 6.47 (dd, J = 2.0, 1.5 Hz, 1H), 5.77 (s, 1H), 4.99 (s, 2H), 4.21 (q, J = 8.0 Hz, 2H), 3.85 (s, 3H), 1.22 (t, J = 8.0 Hz, 3H). 134 CF.sub.3 [00210]embedded image (500 MHz, Chloroform-d) δ 7.38-7.30 (m, 4H), 7.20-7.08 (m, 3H), 7.05- 6.96 (m, 3H), 5.54 (s, 1H). 135 CF.sub.3 [00211]embedded image (500 MHz, Chloroform-d) δ 7.44-7.27 (m, 8H), 7.07 (s, 1H), 5.54 (s, 1H), 5.12 (s, 2H), 2.24 (s, 3H). 136 CF.sub.3 [00212]embedded image (500 MHz, Chloroform-d) δ 7.66 (d, J = 2.0 Hz, 1H), 7.49-7.27 (m, 6H), 7.17 (d, J = 7.5 Hz, 1H), 7.01 (s, 1H), 5.81 (s, 1H), 5.11 (s, 2H). 137 CF.sub.3 [00213]embedded image (500 MHz, Chloroform-d) δ 7.56 (d, J = 7.0 Hz, 2H), 7.50 (d, J = 7.0 Hz, 2H), 7.06 (s, 1H), 5.56 (s, 1H), 3.53 (s, 3H). 138 CF.sub.3 [00214]embedded image 139 CF.sub.3 [00215]embedded image (500 MHz, Chloroform-d) δ 8.03 (d, J = 7.5 Hz, 2H), 7.91 (d, J = 7.5 Hz, 2H), 7.01 (s, 1H), 5.79 (s, 1H), 3.51 (d, J = 7.0 Hz, 2H), 1.41-1.31 (m, 1H), 0.51- 0.39 (m, 2H), 0.36-0.26 (m, 2H). 140 CF.sub.3 [00216]embedded image (500 MHz, Chloroform-d) δ 7.33-7.23 (m, 3H), 7.08-7.00 (m, 2H), 5.60 (s, 1H), 4.88 (s, 2H), 4.02 (hept, J = 7.0 Hz, 1H), 3.72 (q, J = 8.0 Hz, 2H), 1.29 (d, J = 7.0 Hz, 6H), 1.23 (t, J = 8.0 Hz, 3H). 141 CF.sub.3 [00217]embedded image (500 MHz, Chloroform-d) δ 7.04 (s, 1H), 6.97-6.88 (m, 2H), 5.73 (s, 1H), 3.70 (s, 2H), 2.87 (hept, J = 6.5 Hz, 1H), 2.36 (s, 3H), 1.39 (d, J = 6.5 Hz, 6H). 142 CF.sub.3 [00218]embedded image (500 MHz, Chloroform-d) δ 7.52-7.44 (m, 2H), 7.48-7.40 (m, 2H), 7.07 (s, 1H), 6.57-6.48 (m, 2H), 6.40-6.34 (m, 2H), 5.63 (s, 1H), 4.43 (s, 1H), 4.32 (s, 2H), 2.19 (s, 3H). 143 CF.sub.3 [00219]embedded image (500 MHz, Chloroform-d) δ 8.12-8.04 (m, 3H), 7.02 (s, 1H), 5.83 (s, 1H). 144 CF.sub.3 [00220]embedded image (500 MHz, Chloroform-d) δ 8.04 (dd, J = 2.0, 1.5 Hz, 1H), 7.60-7.49 (m, 3H), 7.04 (s, 1H), 6.49-6.21 (m, 1H), 5.73 (s, 1H), 3.14-3.05 (m, 2H). 145 CF.sub.3 [00221]embedded image (500 MHz, Chloroform-d) δ 7.99 (d, J = 7.5 Hz, 2H), 7.91 (d, J = 7.5 Hz, 2H), 7.01 (s, 1H), 5.80 (s, 1H), 4.67 (s, 2H), 2.92 (hept, J = 6.5 Hz, 1H), 1.20-1.15 (m, 7H). 146 CF.sub.3 [00222]embedded image 147 CF.sub.3 [00223]embedded image (500 MHz, Chloroform-d) δ 8.20-8.08 (m, 1H), 7.89 (d, J = 7.5 Hz, 2H), 7.76 (d, J = 7.5 Hz, 2H), 7.49 (dd, J = 7.5, 7.0 Hz, 1H), 7.25-7.14 (m, 2H), 7.05 (s, 1H), 5.63 (s, 1H), 3.40 (s, 3H). 148 CF.sub.3 [00224]embedded image (500 MHz, Chloroform-d) δ 8.18 (dd, J = 2.0, 1.5 Hz, 1H), 7.82-7.77 (m, 2H), 7.65-7.54 (m, 2H), 7.01 (s, 1H), 6.87 (d, J = 1.5 Hz, 1H), 6.48 (d, J = 1.5 Hz, 1H), 5.82 (s, 1H), 3.25 (s, 3H). 149 CF.sub.3 [00225]embedded image 150 CF.sub.3 [00226]embedded image (500 MHz, Chloroform-d) δ 7.52 (d, J = 7.5 Hz, 2H), 7.46 (d, J = 7.5 Hz, 2H), 7.06 (s, 1H), 5.52 (s, 1H), 3.24-3.16 (m, 1H), 2.13-2.01 (m, 2H), 1.75- 1.63 (m, 4H), 1.55-1.38 (m, 2H). 151 CF.sub.3 [00227]embedded image (500 MHz, Chloroform-d) δ 8.06 (d, J = 7.5 Hz, 2H), 7.79 (d, J = 7.5 Hz, 2H), 7.07 (s, 1H), 5.46 (s, 1H), 4.40 (s, 2H). 152 CF.sub.3 [00228]embedded image (500 MHz, Chloroform-d) δ 8.06 (d, J = 7.5 Hz, 2H), 7.87 (d, J = 7.5 Hz, 2H), 7.01 (s, 1H), 5.80 (s, 1H), 4.45 (s, 1H), 2.53 (s, 3H). 153 CF.sub.3 [00229]embedded image (500 MHz, Chloroform-d) δ 7.90-7.78 (m, 2H), 7.67-7.56 (m, 4H), 7.37- 7.29 (m, 3H), 7.06 (s, 1H), 5.66 (s, 1H). 154 CF.sub.3 [00230]embedded image (500 MHz, Chloroform-d) δ 7.68-7.50 (m, 6H), 7.37-7.29 (m, 3H), 6.94 (s, 1H), 5.70 (s, 1H). 155 CF.sub.3 [00231]embedded image (500 MHz, Chloroform-d) δ 8.73 (d, J = 1.5 Hz, 1H), 8.63 (dd, J = 5.0, 1.0 Hz, 1H), 7.94-7.81 (m, 2H), 7.65-7.56 (m, 3H), 7.38-7.29 (m, 1H), 7.07 (s, 1H), 5.62 (s, 1H). 156 CF.sub.3 [00232]embedded image (500 MHz, Chloroform-d) δ 7.87-7.55 (m, 5H), 7.42-7.37 (m, 2H), 7.08 (s, 1H), 5.60 (s, 1H), 2.35 (s, 3H). 157 CF.sub.3 [00233]embedded image 158 CF.sub.3 [00234]embedded image 159 CF.sub.3 [00235]embedded image (500 MHz, Chloroform-d) δ 8.09 (d, J = 7.5 Hz, 2H), 7.87 (d, J = 7.5 Hz, 2H), 7.01 (s, 1H), 5.80 (s, 1H), 3.64-3.51 (m, 4H), 2.96-2.83 (m, 4H). 160 CF.sub.3 [00236]embedded image (500 MHz, Chloroform-d) δ 7.04 (s, 1H), 6.84 (s, 1H), 6.68 (s, 1H), 5.70 (s, 1H), 3.94 (s, 3H), 2.94 (s, 6H), 2.30 (s, 3H). 161 CF.sub.3 [00237]embedded image (500 MHz, Chloroform-d) δ 7.20 (s, 2H), 7.01 (s, 1H), 5.56 (s, 1H), 2.32 (s, 6H). 162 CF.sub.3 [00238]embedded image (500 MHz, Chloroform-d) δ 7.42 (d, J = 7.5 Hz, 1H), 7.36 (d, J = 7.5 Hz, 1H), 7.01 (s, 1H), 5.62 (s, 1H), 2.32 (s, 3H). 163 CF.sub.3 [00239]embedded image (500 MHz, Chloroform-d) δ 7.83 (d, J = 2.5 Hz, 1H), 7.66 (d, J = 2.5 Hz, 1H), 7.06 (s, 1H), 5.38 (s, 1H), 2.88 (q, J = 8.0 Hz, 2H), 1.27 (t, J = 8.0 Hz, 3H). 164 CF.sub.3 [00240]embedded image (500 MHz, Chloroform-d) δ 8.12 (d, J = 2.0 Hz, 1H), 7.63 (d, J = 2.0 Hz, 1H), 7.07 (s, 1H), 5.65 (s, 1H), 2.51 (s, 3H), 1.92-1.83 (m, 1H), 1.20-1.11 (m, 2H), 0.93-0.8l (m, 2H). 165 CF.sub.3 [00241]embedded image (500 MHz, Chloroform-d) δ 7.49 (s, 1H), 7.19 (t, J = 73.5 Hz, 1H), 7.07 (s, 1H), 7.01 (s, 1H), 5.64 (s, 1H). 166 CF.sub.3 [00242]embedded image (500 MHz, Chloroform-d) δ 7.68 (d, J = 10.5 Hz, 1H), 7.41 (d, J = 6.0 Hz, 1H), 7.13-7.09 (m, 2H), 5.58-5.29 (m, 3H). 167 CF.sub.3 [00243]embedded image (500 MHz, Chloroform-d) δ 7.45-7.33 (m, 2H), 7.13 (s, 1H), 6.75 (s, 1H), 5.07 (s, 1H), 3.24 (q, J = 8.0 Hz, 2H), 1.09 (t, J = 8.0 Hz, 3H). 168 CF.sub.3 [00244]embedded image (500 MHz, Chloroform-d) δ 7.62 (s, 2H), 7.54-7.48 (m, 2H), 7.44-7.36 (m, 3H), 7.08 (s, 1H), 5.54 (s, 1H). 169 CF.sub.3 [00245]embedded image .sup.1H NMR (500 MHz, Chloroform-d) δ 7.48-7.38 (m, 1H), 7.22-7.16 (m, 2H), 7.08 (s, 1H), 6.79-6.74 (m, 2H), 5.42 (s, 1H). 170 CF.sub.3 [00246]embedded image (500 MHz, Chloroform-d) δ 8.28 (d, J = 2.0 Hz, 1H), 7.93 (s, 1H), 7.79 (dd, J = 7.5, 2.0 Hz, 1H), 7.20-7.10 (m, 2H), 3.45 (q, J = 6.8 Hz, 2H), 2.83 (s, 6H), 1.40 (t, J = 6.8 Hz, 3H). 171 CF.sub.3 [00247]embedded image (500 MHz, Chloroform-d) δ 7.39 (d, J = 7.5 Hz, 1H), 7.22-7.15 (m, 2H), 7.03 (s, 1H), 5.67 (s, 1H), 3.70 (s, 2H), 2.48 (q, J = 8.0 Hz, 2H), 2.30 (s, 3H), 1.24 (t, J = 8.0 Hz, 3H). 172 CF.sub.3 [00248]embedded image (500 MHz, Chloroform-d) δ 8.01 (d, J = 7.5 Hz, 1H), 7.58 (d, J = 7.5 Hz, 1H), 7.00 (s, 1H), 5.69 (s, 1H), 3.24-3.17 (m, 1H), 3.14 (s, 3H), 2.11-2.00 (m, 2H), 1.77-1.64 (m, 2H), 1.59-1.48 (m, 4H). 173 CF.sub.3 [00249]embedded image (500 MHz, Chloroform-d) δ 7.60 (dd, J = 7.5, 2.0 Hz, 1H), 7.54 (d, J = 7.5 Hz, 1H), 7.36 (d, J = 2.0 Hz, 1H), 6.99 (s, 1H), 5.68 (s, 1H), 3.07 (s, 1H), 2.67 (s, 1H). 174 CF.sub.3 [00250]embedded image (500 MHz, Chloroform-d) δ 7.50-7.40 (m, 2H), 7.26-7.11 (m, 1H), 7.03 (s, 1H), 5.66 (s, 1H), 5.34 (s, 1H), 2.61- 2.51 (m, 1H), 2.19-2.10 (m, 2H), 1.82- 1.71 (m, 4H), 1.54-1.34 (m, 4H). 175 CF.sub.3 [00251]embedded image (500 MHz, Chloroform-d) δ 8.25 (d, J = 2.0 Hz, 1H), 7.92 (d, J = 2.0 Hz, 1H), 7.02 (s, 1H), 5.64 (s, 1H), 3.12 (hept, J = 6.5 Hz, 1H), 1.30 (d, J = 6.5 Hz, 6H). 176 CF.sub.3 [00252]embedded image (500 MHz, Chloroform-d) δ 7.99 (d, J = 1.5 Hz, 1H), 7.66-7.43 (m, 2H), 7.01 (s, 1H), 5.80 (s, 1H), 4.19 (q, J = 8.0 Hz, 2H), 1.34 (t, J = 8.0 Hz, 3H). 177 CF.sub.3 [00253]embedded image (500 MHz, Chloroform-d) δ 7.35-7.29 (m, 2H), 7.06 (s, 1H), 6.96-6.89 (m, 1H), 6.57 (s, 1H), 5.62 (s, 1H). 178 CF.sub.3 [00254]embedded image (500 MHz, Chloroform-d) δ 7.21-7.10 (m, 1H), 7.06 (s, 1H), 6.81-6.62 (m, 2H), 5.39 (s, 1H), 4.39 (s, 1H), 3.87- 3.77 (m, 2H), 3.51-3.34 (m, 2H), 2.99- 2.89 (m, 1H), 1.92-1.71 (m, 2H), 1.27 (d, J = 6.5 Hz, 3H), 0.91 (t, J = 8.0 Hz, 3H). 179 CF.sub.3 [00255]embedded image (500 MHz, Chloroform-d) δ 8.78 (d, J = 11.0 Hz, 1H), 8.08 (d, J = 6.5 Hz, 1H), 7.12 (s, 1H), 5.49 (s, 1H), 2.66 (q, J = 8.0, Hz, 2H), 1.17 (t, J = 8.0 Hz, 3H). 180 CF.sub.3 [00256]embedded image (500 MHz, Chloroform-d) δ 7.10-7.01 (m, 3H), 6.64-6.56 (m, 3H), 5.83- 5.76 (m, 1H), 5.79 (s, 1H), 2.91-2.76 (m, 2H). 181 CF.sub.3 [00257]embedded image (500 MHz, Chloroform-d) δ 7.65 (s, 1H), 7.59 (d, J = 2.0 Hz, 1H), 7.53 (d, J = 7.5 Hz, 1H), 7.45 (dd, J = 7.5, 2.0 Hz, 1H), 7.29 (s, 1H), 6.15 (s, 1H). 182 CF.sub.3 [00258]embedded image (500 MHz, Chloroform-d) δ 8.25-8.17 (m, 3H), 7.33 (s, 1H), 7.10 (s, 1H), 5.54- 5.31 (m, 3H), 4.31 (q, J = 7.5 Hz, 2H), 1.34 (t, J = 7.5 Hz, 3H). 183 CF.sub.3 [00259]embedded image (500 MHz, Chloroform-d) δ 8.27 (s, 1H), 7.85 (dd, J = 7.5, 2.0 Hz, 1H), 7.62 (d, J = 7.5 Hz, 1H), 7.24 (d, J = 2.0 Hz, 1H), 7.02 (s, 1H), 5.72 (s, 1H), 2.10 (s, 3H). 184 CF.sub.3 [00260]embedded image (500 MHz, Chloroform-d) δ 8.33 (d, J = 2.0 Hz, 1H), 7.88 (dd, J = 7.5, 2.0 Hz, 1H), 7.80 (d, J = 7.5 Hz, 1H), 7.57 (d, J = 2.0 Hz, 2H), 7.45-7.37 (m, 1H), 7.08 (s, 1H), 6.46 (s, 2H), 5.62 (s, 1H). 185 CF.sub.3 [00261]embedded image 186 CF.sub.3 [00262]embedded image (500 MHz, Chloroform-d) δ 7.84-7.74 (m, 2H), 7.56 (d, J = 7.5 Hz, 1H), 7.04 (s, 1H), 5.63 (s, 1H), 3.39 (s, 6H), 2.34 (s, 3H). 187 CF.sub.3 [00263]embedded image (500 MHz, Chloroform-d) δ 8.67 (s, 1H), 7.87 (s, 1H), 7.63 (d, J = 7.5 Hz, 1H), 7.42 (dd, J = 7.5, 2.0 Hz, 1H), 7.16 (d, J = 2.0 Hz, 1H), 7.00 (s, 1H), 5.80 (s, 1H). 188 CF.sub.3 [00264]embedded image (500 MHz, Chloroform-d) δ 9.31 (s, 1H), 8.85 (d, J = 5.5 Hz, 1H), 8.75 (d, J = 5.5 Hz, 1H), 8.42-8.38 (m, 1H), 8.32 (dd, J = 7.5, 2.0 Hz, 1H), 7.72 (d, J = 7.5 Hz, 1H), 7.06 (s, 1H), 5.55 (s, 1H). 189 CF.sub.3 [00265]embedded image (500 MHz, Chloroform-d) δ 8.15-8.09 (m, 2H), 7.97-7.81 (m, 1H), 7.35- 7.21 (m, 2H), 7.03 (s, 1H), 6.34-6.20 (m, 2H), 5.84 (s, 1H). 190 CF.sub.3 [00266]embedded image (500 MHz, Chloroform-d) δ 7.63 (d, J = 7.5 Hz, 2H), 7.06 (s, 1H), 6.94 (d, J = 7.5 Hz, 2H), 5.58 (s, 1H), 3.49-3.43 (m, 4H), 1.67-1.57 (m, 6H). 191 CF.sub.3 [00267]embedded image (500 MHz, Chloroform-d) δ 7.23-7.06 (m, 2H), 6.95-6.72 (m, 3H), 5.51 (s, 1H), 3.74-3.55 (m, 4H), 3.33-3, 16 (m, 4H). 192 CF.sub.3 [00268]embedded image (500 MHz, Chloroform-d) δ 8.69 (d, J = 5.0 Hz, 2H), 7.96 (d, J = 5.0 Hz, 2H), 7.86-7.74 (m, 4H), 7.02 (s, 1H), 5.82 (s, 1H). 193 CF.sub.3 [00269]embedded image (500 MHz, Chloroform-d) δ 9.17 (s, 1H), 9.08 (s, 2H), 7.98-7.82 (m, 1H), 7.65-7.38 (m, 3H), 7.12 (s, 1H), 5.67 (s, 1H). 194 CF.sub.3 [00270]embedded image (500 MHz, Chloroform-d) δ 7.64-7.57 (m, 2H), 7.37 (d, J = 2.0 Hz, 1H), 7.06- 7.00 (m, 2H), 6.68-6.54 (m, 2H), 6.14 (s, 1H), 3.87 (s, 3H). 195 CF.sub.3 [00271]embedded image (500 MHz, Chloroform-d) δ 7.61 (d, J = 2.0 Hz, 1H), 7.50 (d, J = 2.0 Hz, 1H), 7.30 (d, J = 2.5 Hz, 1H), 7.05 (s, 1H), 6.71 (d, J = 2.5 Hz, 1H), 2.36 (s, 3H). 196 CF.sub.3 [00272]embedded image (500 MHz, Chloroform-d) δ 7.78 (s, 1H), 7.47-7.41 (m, 2H), 7.32-7.25 (m, 2H), 7.09 (s, 1H), 6.34-6.23 (m, 1H), 5.60 (s, 1H). 197 CF.sub.3 [00273]embedded image 198 CF.sub.3 [00274]embedded image (500 MHz, Chloroform-d) δ 8.97 (s, 1H), 7.96 (d, J = 7.5 Hz, 2H), 7.85 (s, 1H), 7.83 (d, J = 7.5 Hz, 2H), 7.02 (s, 1H), 5.82 (s, 1H). 199 CF.sub.3 [00275]embedded image (500 MHz, Chloroform-d) δ 8.53 (s, 1H), 8.43 (s, 1H), 7.64 (s, 2H), 7.04 (s, 1H), 5.64 (s, 1H). 200 CF.sub.3 [00276]embedded image (500 MHz, Chloroform-d) δ 8.32 (s, 1H), 7.89 (d, J = 2.0 Hz, 1H), 7.64 (dd, J = 7.5, 2.0 Hz, 1H), 7.31 (d, J = 7.5 Hz, 1H), 7.04 (s, 1H), 2.67 (s, 3H). 201 CF.sub.3 [00277]embedded image (500 MHz, Chloroform-d) δ 7.64-7.57 (m, 2H), 7.37 (d, J = 2.0 Hz, 1H), 7.06- 6.99 (m, 2H), 6.69-6.54 (m, 2H), 6.14 (s, 1H), 3.87 (s, 3H). 202 CF.sub.3 [00278]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 12.37 (s, 1H), 9.18 (d, J = 2.5 Hz, 1H), 8.68- 8.56 (m, 2H), 7.56-7.41 (m, 1H), 7.28 (s, 1H). 203 CF.sub.3 [00279]embedded image (500 MHz, Chloroform-d) δ 8.68 (d, J = 5.0 Hz, 1H), 7.56-7.50 (m, 2H), 7.24 (s, 1H), 5.80 (s, 1H), 2.69 (s, 3H). 204 CF.sub.3 [00280]embedded image .sup.1H NMR (500 MHz, DMSO-d6) δ 12.66 (s, 1H), 8.79 (s, 1H), 8.55 (d, J = 5.0 Hz, 1H), 7.46 (dd, J = 5.0 Hz, 1H), 7.26 (s, 1H). 205 CF.sub.3 [00281]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.09 (s, 1H), 8.55-8.43 (m 1H), 8.02-7.89 (m, 1H), 7.59-7.40 (m, 1H), 7.36 (s, 1H). 206 CF.sub.3 [00282]embedded image (500 MHz, Chloroform-d) δ 8.45 (dd, J = 5.5, 5.0 Hz, 1H), 7.63-7.52 (m, 1H), 7.42 (dd, J = 8.0, 1.0 Hz, 1H), 7.30 (s, 1H), 5.34 (s, 1H). 207 CF.sub.3 [00283]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.65 (s, 1H), 8.80-8.57 (m, 2H), 7.36-7.34 (m, 2H). 208 CF.sub.3 [00284]embedded image (500 MHz, Chloroform-d) δ 9.20 (d, J = 1.5 Hz, 1H), 9.07 (d, J = 2.0 Hz, 1H), 8.40 (dd, J = 2.0, 1.5 Hz, 1H), 8.40 (s, 1H), 7.31 (s, 1H), 5.41 (s, 1H). 209 CF.sub.3 [00285]embedded image (500 MHz, Chloroform-d) δ 9.09 (d, J = 1.5 Hz, 1H), 8.02 (dd, J = 8.0, 1.5 Hz, 1H), 7.47 (d, J = 8.0 Hz, 1H), 7.30 (s, 1H), 5.34 (s, 1H), 3.26 (t, J = 8.0 Hz, 2H), 1.86-1.67 (m, 2H), 1.01 (t, J = 8.0 Hz, 3H). 210 CF.sub.3 [00286]embedded image (500 MHz, Chloroform-d) δ 8.61 (dd, J = 5.0, 1.5 Hz, 1H), 7.85 (dd, J = 8.0, 1.5 Hz, 1H), 7.49 (dd, J = 8.0, 5.0 Hz, 1H), 7.25 (s, 1H), 6.72 (dd, J = 16.5, 10.0 Hz, 1H), 6.19 (dd, J = 13.5, 10.0 Hz, 1H), 5.67 (dd, J = 16.5, 13.5 Hz, 1H), 5.60 (s, 1H). 211 CF.sub.3 [00287]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.41 (s, 1H), 8.97 (s, 1H), 8.52 (s, 1H), 8.20 (s, 1H), 7.29 (s, 1H), 2.38 (s, 3H). 212 CF.sub.3 [00288]embedded image (500 MHz, Chloroform-d) δ 9.18 (d, J = 1.5 Hz, 1H), 8.24 (dd, J = 8.0, 1.5 Hz, 1H), 8.02 (d, J = 8.0 Hz, 1H), 7.32 (s, 1H), 5.20 (s, 1H). 213 CF.sub.3 [00289]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 12.45 (s, 1H), 8.32 (dd, J = 5.0, 1.5 Hz, 1H), 7.79 (dd, J = 6.5, 1.5 Hz, 1H), 7.36 (s, 1H), 7.11 (dd, J = 6.5, 5.0 Hz, 1H), 4.32 (q, J = 7.0 Hz, 2H), 1.19 (t, J = 7.0 Hz, 3H). 214 CF.sub.3 [00290]embedded image (500 MHz, Chloroform-d) δ 8.91 (s, 1H), 8.53 (s, 1H), 7.80 (s, 1H), 7.24 (s, 1H), 5.81 (s, 1H), 1.71-1.60 (m, 1H), 1.07-0.98 (m, 2H), 0.79-0.70 (m, 2H). 215 CF.sub.3 [00291]embedded image (500 MHz, Chloroform-d) δ 9.19 (d, J = 1.5 Hz, 1H), 8.11 (dd, J = 7.0, 1.5 Hz, 1H), 7.52 (d, J = 7.0 Hz, 1H), 7.30 (s, 1H), 5.36 (s, 1H), 2.61-2.42 (m, 2H), 1.85-1.73 (m, 7H), 1.28-1.20 (m, 2H). 216 CF.sub.3 [00292]embedded image 217 CF.sub.3 [00293]embedded image (500 MHz, Chloroform-d) δ 8.80 (d, J = 1.5 Hz, 1H), 8.48 (d, J = 2.0 Hz, 1H), 7.87 (dd, J = 2.0, 1.5 Hz, 1H), 7.28 (s, 1H), 5.51 (s, 1H), 4.72-4.16 (m, 3H), 3.00-2.76 (m, 2H). 218 CF.sub.3 [00294]embedded image (500 MHz, Chloroform-d) δ 7.93 (s, 2H), 7.26 (s, 1H), 5.74 (s, 1H). 219 CF.sub.3 [00295]embedded image (500 MHz, Chloroform-d) δ 8.75 (dd, J = 4.5, 1.5 Hz, 1H), 7.76 (dd, J = 6.0, 1.5 Hz, 1H), 7.24 (s, 1H), 5.81 (s, 1H), 2.33 (s, 3H). 220 CF.sub.3 [00296]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.36 (s, 1H), 7.52 (s, 1H), 7.45-7.25 (m, 2H). 221 CF.sub.3 [00297]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.40 (s, 1H), 8.20 (d, J = 4.5 Hz, 1H), 7.34 (d, J = 10.5 Hz, 1H), 7.22 (s, 1H), 2.22 (s, 3H). 222 CF.sub.3 [00298]embedded image (500 MHz, Chloroform-d) δ 8.48 (d, J = 5.0 Hz, 1H), 7.74 (d, J = 5.0 Hz, 1H), 7.24 (s, 1H), 5.68 (s, 1H). 223 CF.sub.3 [00299]embedded image (500 MHz, Chloroform-d) δ 8.11 (dd, J = 8.0, 5.0 Hz, 1H), 7.24 (s, 1H), 6.84 (dd, J = 8.0, 7.5 Hz, 1H), 5.67 (s, 1H), 2.83 (s, 3H). 224 CF.sub.3 [00300]embedded image (500 MHz, Chloroform-d) δ 8.11 (s, 1H), 7.24 (s, 1H), 6.84 (s, 1H), 5.67 (s, 1H). 225 CF.sub.3 [00301]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.59 (s, 1H), 8.87 (s, 1H), 8.42 (s, 1H), 7.33 (s, 1H), 2.43 (s, 3H). 226 CF.sub.3 [00302]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.16 (s, 1H), 8.88 (d, J = 2.5 Hz, 1H), 8.35 (dd, J = 8.5, 2.5 Hz, 1H), 7.29 (s, 1H), 6.98 (d, J = 8.5 Hz, 1H), 3.93 (s, 3H). 227 CF.sub.3 [00303]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 12.61 (s, 1H), 8.33 (d, J = 5.0 Hz, 1H), 7.82 (d, J = 7.5 Hz, 1H), 7.33 (s, 1H), 7.16 (dd, J = 7.5, 5.0 Hz, 1H), 3.84 (s, 3H). 228 CF.sub.3 [00304]embedded image (500 MHz, Chloroform-d) δ 8.02 (s, 1H), 7.30 (s, 1H), 5.42 (s, 1H), 4.76- 4.38 (m, 2H), 3.19-3.02 (m, 1H), 2.08- 1.94 (m, 2H), 1.39 (d, J = 7.0 Hz, 3H). 229 CF.sub.3 [00305]embedded image (500 MHz, Chloroform-d) δ 8.96 (s, 1H), 7.53 (s, 1H), 7.23 (s, 1H), 6.89 (s, 1H), 5.80 (s, 1H), 4.47-4.37 (m, 2H), 3.08-2.91 (m, 2H). 230 CF.sub.3 [00306]embedded image 231 CF.sub.3 [00307]embedded image (500 MHz, Chloroform-d) δ 8.56 (s, 1H), 7.41 (s, 1H), 7.35 (s, 1H), 4.45 (s, 1H), 3.50 (s, 1H), 3.11-3.01 (m, 1H), 0.65-0.55 (m, 2H), 0.43-0.31 (m, 2H). 232 CF.sub.3 [00308]embedded image (500 MHz, Chloroform-d) δ 8.42 (s, 1H), 7.25 (s, 1H), 7.11 (s, 1H), 5.68 (s, 1H), 4.90 (hept, J = 7.0 Hz, 1H), 1.29 (d, J = 7.0 Hz, 6H). 233 CF.sub.3 [00309]embedded image (500 MHz, Chloroform-d) δ 8.00 (d, J = 1.5 Hz, 1H), 7.52 (d, J = 1.5 Hz, 1H), 7.29 (s, 1H), 5.17 (s, 1H), 5.03 (q, J = 7.0 Hz, 2H), 2.98 (hept, J = 7.5 Hz, 1H), 1.30 (d, J = 7.5 Hz, 6H). 234 CF.sub.3 [00310]embedded image (500 MHz, Chloroform-d) δ 7.92 (d, J = 8.0 Hz, 1H), 7.24 (s, 1H), 6.92 (d, J = 8.0 Hz, 1H), 5.68 (s, 1H), 4.68 (s, 2H), 2.99 (s, 1H). 235 CF.sub.3 [00311]embedded image (500 MHz, Chloroform-d) δ 8.66 (d, J = 1.0 Hz, 1H), 8.61 (d, J = 1.5 Hz, 1H), 7.90 (dd, J = 1.5, 1.0 Hz, 1H), 7.32 (s, 1H), 5.20 (s, 1H), 2.39-2.26 (m, 1H), 1.05-0.95 (m, 2H), 0.53-0.44 (m, 2H). 236 CF.sub.3 [00312]embedded image (500 MHz, Chloroform-d) δ 8.88 (d, J = 1.5 Hz, 1H), 7.94 (dd, J = 8.0, 1.5 Hz, 1H), 7.38 (d, J = 8.0 Hz, 1H), 7.23 (s, 1H), 5.78 (s, 1H), 2.97 (q, J = 8.0 Hz, 2H), 1.36 (t, J = 8.0 Hz, 3H). 237 CF.sub.3 [00313]embedded image 238 CF.sub.3 [00314]embedded image (500 MHz, Chloroform-d) δ 8.89 (d, J = 1.0 Hz, 1H), 7.94 (dd, J = 8.0, 1.0 Hz, 1H), 7.39 (d, J = 8.0 Hz, 1H), 7.23 (s, 1H), 5.79 (s, 1H), 3.78 (t, J = 7.5 Hz, 2H), 3.21 (t, J = 7.5 Hz, 2H). 239 CF.sub.3 [00315]embedded image (500 MHz, Chloroform-d) δ 9.14 (d, J = 1.0 Hz, 1H), 8.04-7.96 (m, 2H), 7.77- 7.71 (m, 2H), 7.31-7.22 (m, 3H), 5.59 (s, 1H), 2.33 (s, 3H). 240 CF.sub.3 [00316]embedded image (500 MHz, Chloroform-d) δ 8.66 (d, J = 1.0 Hz, 1H), 7.87 (dd, J = 8.0, 1.0 Hz, 1H), 7.47-7.39 (m, 2H), 7.31 (s, 1H), 7.18-7.12 (m, 2H), 7.09 (d, J = 8.0 Hz, 1H), 6.96-6.83 (m, 1H), 5.37 (s, 1H). 241 CF.sub.3 [00317]embedded image (500 MHz, Chloroform-d) δ 9.22 (d, J = 1.0 Hz, 1H), 8.11 (dd, J = 8.0, 1.0 Hz, 1H), 7.54 (d, J = 8.0 Hz, 1H), 7.32- 7.23 (m, 3H), 7.19-7.11 (m, 1H), 7.14- 7.06 (m, 2H), 5.32 (s, 1H), 4.21 (s, 2H). 242 CF.sub.3 [00318]embedded image (500 MHz, Chloroform-d) δ 8.69 (d, J = 1.0 Hz, 1H), 7.85 (dd, J = 8.0, 1.0 Hz, 1H), 7.48-7.40 (m, 3H), 7.33-7.27 (m, 2H), 6.97 (d, J = 8.0 Hz, 1H), 5.31 (s, 1H). 243 CF.sub.3 [00319]embedded image (500 MHz, Chloroform-d) δ 9.07 (s, 1H), 7.23 (s, 1H), 7.06 (s, 1H), 5.75 (s, 1H), 4.04 (s, 2H), 3.50 (s, 2H), 2.47 (q, J = 8.0 Hz, 2H), 1.22 (t, J = 8.0 Hz, 3H). 244 CF.sub.3 [00320]embedded image (500 MHz, Chloroform-d) δ 8.23 (d, J = 8.0 Hz, 1H), 7.71 (d, J = 8.0 Hz, 1H), 7.36 (s, 1H), 6.70 (s, 1H), 3.98 (s, 3H), 3.28 (s, 6H). 245 CF.sub.3 [00321]embedded image (500 MHz, Chloroform-d) δ 9.26 (s, 1H), 8.62 (s, 1H), 7.54 (s, 1H), 7.42 (s, 1H), 7.36-7.25 (m, 2H), 7.22-7.11 (m, 2H), 3.18 (s, 3H). 246 CF.sub.3 [00322]embedded image (500 MHz, Chloroform-d) δ 9.13 (d, J = 1.0 Hz, 1H), 8.44 (d, J = 8.0 Hz, 1H), 8.15 (dd, J = 8.0, 1.0 Hz, 1H), 7.83 (s, 1H), 7.30 (s, 1H), 5.42 (s, 1H), 2.16 (s, 3H). 247 CF.sub.3 [00323]embedded image (500 MHz, Chloroform-d) δ 8.92 (d, J = 1.0 Hz, 1H), 8.61 (d, J = 1.5 Hz, 1H), 7.98 (dd, J = 1.5, 1.0 Hz, 1H), 7.24 (s, 1H), 5.83 (s, 1H), 5.72 (s, 2H), 3.52 (s, 2H). 248 CF.sub.3 [00324]embedded image (500 MHz, Chloroform-d) δ 9.08 (d, J = 1.0 Hz, 1H), 8.05 (dd, J = 8.0, 1.0 Hz, 1H), 7.37-7.18 (m, 5H), 7.03-6.92 (m, 1H), 6.78 (d, J = 8.0 Hz, 1H), 5.83 (s, 1H), 3.70 (s, 3H). 249 CF.sub.3 [00325]embedded image (500 MHz, Chloroform-d) δ 9.29 (d, J = 1.0 Hz, 1H), 8.22 (dd, J = 8.0, 1.0 Hz, 1H), 7.56-7.46 (m, 3H), 7.33-7.20 (m, 1H), 7.24 (s, 2H), 5.79 (s, 1H), 4.21 (s, 2H). 250 CF.sub.3 [00326]embedded image (500 MHz, Chloroform-d) δ 8.71 (d, J = 1.0 Hz, 1H), 7.84 (dd, J = 8.0, 1.0 Hz, 1H), 7.48-7.40 (m, 4H), 7.31 (s, 1H), 6.98 (d, J = 8.0 Hz, 1H), 5.38 (s, 1H), 5.31 (s, 2H). 251 CF.sub.3 [00327]embedded image (500 MHz, Chloroform-d) δ 9.15 (d, J = 1.0 Hz, 1H), 8.10 (dd, J = 8.0, 1.0 Hz, 1H), 7.24 (s, 1H), 7.23-7.15 (m, 2H), 6.95-6.88 (m, 2H), 6.82-6.74 (m, 2H), 5.89 (s, 1H), 2.86 (s, 3H). 252 CF.sub.3 [00328]embedded image (500 MHz, Chloroform-d) δ 8.94 (d, J = 1.0 Hz, 1H), 7.90 (dd, J = 8.0, 1.0 Hz, 1H), 7.28 (s, 1H), 6.58 (d, J = 8.0 Hz, 1H), 5.51 (s, 1H), 4.48 (s, 2H), 3.26 (q, J = 8.0 Hz, 2H), 2.13 (s, 3H), 0.93 (t, J = 8.0 Hz, 3H). 253 CF.sub.3 [00329]embedded image (500 MHz, Chloroform-d) δ 8.61 (d, J = 1.0 Hz, 1H), 7.88 (dd, J = 8.0, 1.0 Hz, 1H), 7.23 (s, 1H), 6.92 (d, J = 8.0 Hz, 1H), 5.78 (s, 1H), 5.08 (d, J = 63.5 Hz, 2H). 254 CF.sub.3 [00330]embedded image (500 MHz, Chloroform-d) δ 9.23 (d, J = 1.0 Hz, 1H), 8.25 (dd, J = 8.0, 1.0 Hz, 1H), 8.19 (d, J = 8.0 Hz, 1H), 7.26 (s, 1H), 5.70 (s, 1H), 4.65 (s, 2H). 255 CF.sub.3 [00331]embedded image (500 MHz, Chloroform-d) δ 9.23 (d, J = 1.0 Hz, 1H), 8.18 (dd, J = 8.0, 1.0 Hz, 1H), 7.31 (d, J = 8.0 Hz, 1H), 7.23 (s, 1H), 5.78 (s, 1H), 4.04 (s, 2H), 3.58 (t, J = 8.0 Hz, 2H), 2.95 (t, J = 8.0 Hz, 2H). 256 CF.sub.3 [00332]embedded image (500 MHz, Chloroform-d) δ 8.96 (d, J = 1.5 Hz, 1H), 7.97 (dd, J = 8.0, 1.5 Hz, 1H), 7.24 (s, 1H), 6.58 (d, J = 8.0 Hz, 1H), 5.80 (s, 1H), 5.44 (s, 2H), 3.45 (q, J = 8.0 Hz, 2H), 3.24 (s, 3H), 1.33 (t, J = 8.0 Hz, 3H). 257 CF.sub.3 [00333]embedded image (500 MHz, Chloroform-d) δ 8.91 (d, J = 1.0 Hz, 1H), 7.89 (dd, J = 7.5, 1.0 Hz, 1H), 7.23 (s, 1H), 6.78 (d, J = 7.5 Hz, 1H), 5.66 (s, 1H), 2.86 (s, 3H), 2.27 (q, J = 8.0 Hz, 2H), 1.07 (t, J = 8.0 Hz, 3H). 258 CF.sub.3 [00334]embedded image 259 CF.sub.3 [00335]embedded image 260 CF.sub.3 [00336]embedded image 261 CF.sub.3 [00337]embedded image (500 MHz, Chloroform-d) δ 8.86 (d, J = 1.0 Hz, 1H), 8.63 (d, J = 1.5 Hz, 1H), 8.00 (dd, J = 1.5, 1.0 Hz, 1H), 7.31 (s, 1H), 5.22 (s, 1H), 4.54 (s, 2H), 4.31- 3.54 (m, 4H). 262 CF.sub.3 [00338]embedded image (500 MHz, Chloroform-d) δ 8.41 (d, J = 1.0 Hz, 1H), 8.09 (d, J = 1.5 Hz, 1H), 7.29-7.21 (m, 2H), 6.00-5.78 (m, 1H), 5.29-5.10 (m, 2H), 4.26 (s, 1H), 3.99-3.77 (m, 2H). 263 CF.sub.3 [00339]embedded image (500 MHz, Chloroform-d) δ 8.41 (dd, J = 5.5, 1.0 Hz, 1H), 8.09-8.00 (m, 2H), 7.29-7.21 (m, 2H), 5.78 (s, 1H). 264 CF.sub.3 [00340]embedded image (500 MHz, Chloroform-d) δ 8.26 (dd, J = 8.0, 1.0 Hz, 1H), 8.04 (dd, J = 7.5, 1.0 Hz, 1H), 7.92 (dd, J = 8.0, 7.5 Hz, 1H), 7.14 (s, 1H), 5.76 (s, 1H). 265 CF.sub.3 [00341]embedded image (500 MHz, Chloroform-d) δ 8.75 (dd, J = 5.0, 1.0 Hz, 1H), 7.85 (dd, J = 8.0, 1.0 Hz, 1H), 7.49 (dd, J = 8.0, 5.0 Hz, 1H), 7.14 (s, 1H), 5.46 (s, 1H). 266 CF.sub.3 [00342]embedded image (500 MHz, Chloroform-d) δ 8.67 (d, J = 5.0 Hz, 1H), 7.45 (dd, J = 5.0, 1.0 Hz, 1H), 7.28 (d, J = 1.0 Hz, 1H), 7.12 (s, 1H), 5.66 (s, 1H), 2.38 (s, 3H). 267 CF.sub.3 [00343]embedded image 268 CF.sub.3 [00344]embedded image (500 MHz, Chloroform-d) δ 8.60 (dd, J = 5.0, 1.0 Hz, 1H), 7.54 (dd, J = 8.0, 1.0 Hz, 1H), 7.37 (dd, J = 8.0, 5.0 Hz, 1H), 7.14 (s, 1H), 5.36 (s, 1H), 3.38-3.29 (m, 1H), 2.04-1.92 (m, 4H), 1.74- 1.57 (m, 4H). 269 CF.sub.3 [00345]embedded image (500 MHz, Chloroform-d) δ 8.52 (d, J = 1.0 Hz, 1H), 7.82 (d, J = 8.0 Hz, 1H), 7.56 (dd, J = 8.0, 1.0 Hz, 1H), 7.08 (s, 1H), 5.73 (s, 1H), 2.47 (d, J = 7.5 Hz, 2H), 1.94-1.82 (m, 1H), 0.92 (d, J = 7.0 Hz, 6H). 270 CF.sub.3 [00346]embedded image (500 MHz, Chloroform-d) δ 7.61 (dd, J = 8.0, 7.5 Hz, 1H), 7.23 (dd, J = 8.0, 1.0 Hz, 1H), 7.13 (s, 1H), 6.87 (dd, J = 8.0, 1.0 Hz, 1H), 5.75 (s, 1H), 5.03 (q, J = 9.0 Hz, 2H). 271 CF.sub.3 [00347]embedded image (500 MHz, Chloroform-d) δ 7.65 (dd, J = 8.0, 7.5 Hz, 1H), 7.26 (dd, J = 8.0, 1.0 Hz, 1H), 7.17 (s, 1H), 6.89 (dd, J = 8.0, 1.0 Hz, 1H), 5.98 (s, 1H), 5.86-5.66 (m, 1H), 4.32-4.26 (m, 2H). 272 CF.sub.3 [00348]embedded image 273 CF.sub.3 [00349]embedded image 274 CF.sub.3 [00350]embedded image (500 MHz, Chloroform-d) δ 7.11 (s, 1H), 6.58 (s, 1H), 6.15 (s, 1H), 4.71 (s, 1H), 2.84 (s, 3H), 2.28 (s, 3H). 275 CF.sub.3 [00351]embedded image (500 MHz, Chloroform-d) δ 7.11 (s, 1H), 6.58 (dd, J = 10.5, 7.5 Hz, 1H), 6.15 (dd, J = 7.5, 5.5 Hz, 1H), 5.71 (s, 1H), 2.28 (s, 3H). 276 CF.sub.3 [00352]embedded image (500 MHz, Chloroform-d) δ 8.23 (d, J = 1.0 Hz, 1H), 8.05 (d, J = 1.0 Hz, 1H), 7.10 (s, 1H), 5.82 (s, 1H), 4.04 (s, 2H), 3.12 (s, 3H), 2.47 (q, J = 8.0 Hz, 2H), 1.24 (t, J = 8.0 Hz, 3H). 277 CF.sub.3 [00353]embedded image (500 MHz, Chloroform-d) δ 8.72 (d, J = 1.0 Hz, 1H), 8.01 (d, J = 8.0 Hz, 1H), 7.81 (dd, J = 8.0, 1.0 Hz, 1H), 7.12 (s, 1H), 5.62 (s, 1H), 4.54 (s, 2H), 4.31- 4.21 (m, 2H), 3.60-3.54 (m, 2H). 278 CF.sub.3 [00354]embedded image (500 MHz, Chloroform-d) δ 8.54 (d, J = 5.1 Hz, 2H), 7.68 (d, J = 5.1 Hz, 2H), 7.31 (s, 1H), 5.31 (s, 1H). 279 CF.sub.3 [00355]embedded image (500 MHz, Chloroform-d) δ 8.58-8.49 (m, 2H), 7.61 (d, J = 5.0 Hz, 1H), 7.27 (s, 1H), 5.82 (s, 1H). 280 CF.sub.3 [00356]embedded image (500 MHz, Chloroform-d) δ 8.65 (d, J = 5.0 Hz, 1H), 7.58 (d, J = 1.0 Hz, 1H), 7.46 (dd, J = 5.0, 1.0 Hz, 1H), 7.30 (s, 1H), 5.35 (s, 1H), 1.33 (s, 9H). 281 CF.sub.3 [00357]embedded image (500 MHz, Chloroform-d) δ 8.12 (d, J = 5.0 Hz, 1H), 7.24 (s, 1H), 7.13 (d, J = 1.0 Hz, 1H), 7.01 (dd, J = 5.0, 1.0 Hz, 1H), 5.81 (s, 1H), 4.90 (hept, J = 7.0 Hz, 1H), 1.29 (d, J = 7.0 Hz, 6H). 282 CF.sub.3 [00358]embedded image (500 MHz, Chloroform-d) δ 8.67 (d, J = 8.0 Hz, 1H), 7.41 (d, J = 5.0 Hz, 1H), 7.26 (s, 1H), 6.31 (s, 1H), 4.12-4.02 (m, 2H), 3.43-3.31 (m, 1H), 1.79- 1.73 (m, 2H), 1.33 (d, J = 7.0 Hz, 3H). 283 CF.sub.3 [00359]embedded image 284 CF.sub.3 [00360]embedded image (500 MHz, Chloroform-d) δ 8.05 (d, J = 1.0 Hz, 1H), 7.67 (d, J = 1.0 Hz, 1H), 7.26 (s, 1H), 5.96-5.86 (m, 1H), 5.84 (s, 1H), 4.30-4.20 (m, 2H). 285 CF.sub.3 [00361]embedded image (500 MHz, Chloroform-d) δ 8.73 (d, J = 5.0 Hz, 1H), 7.76 (d, J = 5.0 Hz, 1H), 7.24 (s, 1H), 5.62 (s, 1H), 2.66 (q, J = 8.0 Hz, 2H), 2.45 (s, 3H), 1.22 (t, J = 8.0 Hz, 3H). 286 CF.sub.3 [00362]embedded image (500 MHz, Chloroform-d) δ 8.61 (s, 1H), 8.34 (s, 1H), 7.36 (s, 1H), 6.36 (s, 1H), 4.52 (s, 2H), 3.58 (q, J = 8.0 Hz, 2H), 3.26 (q, J = 8.0 Hz, 2H), 2.95 (s, 3H), 1.15 (d, J = 8.0 Hz, 3H), 1.10 (d, J = 8.0 Hz, 3H). 287 CF.sub.3 [00363]embedded image (500 MHz, Chloroform-d) δ 8.37 (s, 1H), 7.46-7.40 (m, 2H), 7.44-7.34 (m, 2H), 7.37-7.27 (m, 1H), 7.31 (s, 1H), 7.18 (s, 1H), 5.66 (s, 1H), 5.28 (s, 2H), 2.32 (s, 3H). 288 CF.sub.3 [00364]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.15 (s, 1H), 8.89 (d, J = 2.0 Hz, 1H), 8.25 (dd, J = 7.0, 2.0 Hz, 1H), 7.19 (s, 1H), 6.94 (d, J = 7.0 Hz, 1H), 3.69-3.57 (m, 4H), 3.55-3.38 (m, 4H). 289 CF.sub.3 [00365]embedded image (500 MHz, Chloroform-d) δ 8.31 (s, 1H), 7.26 (s, 1H), 6.96 (s, 1H), 6.80- 6.61 (m, 1H), 5.85 (s, 1H), 5.72-5.43 (m, 2H), 2.32 (s, 3H). 290 CF.sub.3 [00366]embedded image (500 MHz, Chloroform-d) δ 8.29 (s, 1H), 7.25 (s, 1H), 5.75 (s, 1H), 4.07 (q, J = 8.0 Hz, 4H), 2.48 (s, 3H), 1.20 (t, J = 8.0 Hz, 6H). 291 CF.sub.3 [00367]embedded image (500 MHz, Chloroform-d) δ 8.38 (d, J = 5.0 Hz, 1H), 8.31 (s, 1H), 7.62 (d, J = 5.0 Hz, 1H), 7.29 (t, J = 73.5 Hz, 1H), 7.25 (s, 2H), 7.02 (s, 1H), 5.70 (s, 1H). 292 CF.sub.3 [00368]embedded image (500 MHz, Chloroform-d) δ 8.87 (d, J = 1.0 Hz, 1H), 8.55 (d, J = 1.5 Hz, 1H), 7.98 (dd, J = 1.5, 1.0 Hz, 1H), 7.28 (s, 1H), 5.72 (s, 1H), 4.52 (s, 2H), 3.36 (s, 3H). 293 CF.sub.3 [00369]embedded image 294 CF.sub.3 [00370]embedded image (500 MHz, Chloroform-d) δ 8.83 (d, J = 5.0 Hz, 1H), 8.42 (d, J = 1.0 Hz, 1H), 7.98 (dd, J = 5.0, 1.0 Hz, 1H), 7.24 (s, 1H), 5.79 (s, 1H), 3.55 (s, 2H), 2.20 (s, 3H). 295 CF.sub.3 [00371]embedded image (500 MHz, Chloroform-d) δ 9.11 (d, J = 1.0 Hz, 1H), 8.05 (dd, J = 8.0, 1.0 Hz, 1H), 7.32-7.23 (m, 2H), 5.38 (s, 1H), 4.03 (s, 2H), 2.48 (q, J = 8.0 Hz, 2H), 1.27 (t, J = 8.0 Hz, 3H). 296 CF.sub.3 [00372]embedded image (500 MHz, Chloroform-d) δ 7.73 (d, J = 1.0 Hz, 1H), 7.53 (d, J = 1.0 Hz, 1H), 7.11 (s, 1H), 3.77 (s, 2H), 2.91 (s, 3H). 297 CF.sub.3 [00373]embedded image 298 CF.sub.3 [00374]embedded image 299 CF.sub.3 [00375]embedded image 300 CF.sub.3 [00376]embedded image (500 MHz, Chloroform-d) δ 9.06 (s, 1H), 8.82 (d, J = 5.0 Hz, 1H), 7.94 (dd, J = 2.0, 1.5 Hz, 1H), 7.75 (d, J = 5.0 Hz, 1H), 7.55 (dd, J = 2.5, 1.5 Hz, 1H), 7.44 (dd, J = 2.5, 2.0 Hz, 1H), 7.28 (s, 1H), 5.63 (s, 1H), 3.81 (s, 3H), 3.12 (s, 3H). 301 CF.sub.3 [00377]embedded image (500 MHz, Chloroform-d) δ 9.11 (d, J = 1.0 Hz, 1H), 8.96 (d, J = 1.5 Hz, 1H), 8.36 (dd, J = 1.5, 1.0 Hz, 1H), 7.68- 7.63 (m, 1H), 7.25 (s, 1H), 7.09-6.92 (m, 2H), 5.89 (s, 1H), 4.33 (s, 1H), 3.95 (s, 3H), 2.83 (s, 3H). 302 CF.sub.3 [00378]embedded image (500 MHz, Chloroform-d) δ 7.90 (d, J = 1.0 Hz, 1H), 7.76 (d, J = 2.5 Hz, 1H), 7.48 (d, J = 1.0 Hz, 1H), 7.13 (s, 1H), 6.75 (d, J = 2.5 Hz, 1H), 2.69 (s, 3H). 303 CF.sub.3 [00379]embedded image (500 MHz, Chloroform-d) δ 8.76 (d, J = 5.0 Hz, 1H), 7.77 (d, J = 1.0 Hz, 1H), 7.64 (dd, J = 5.0, 1.0 Hz, 1H), 7.27 (d, J = 2.5 Hz, 1H), 7.24 (s, 1H), 7.00 (dd, J = 2.5, 2.0 Hz, 1H), 6.88 (d, J = 2.0 Hz, 1H), 5.80 (s, 1H), 4.41 (s, 2H). 304 CF.sub.3 [00380]embedded image 305 CF.sub.3 [00381]embedded image (500 MHz, Chloroform-d) δ 8.66 (d, J = 1.5 Hz, 1H), 7.83 (d, J = 8.0 Hz, 1H), 7.66 (dd, J = 8.0, 1.5 Hz, 1H), 7.10 (s, 1H), 5.44 (s, 1H), 4.67 (s, 2H), 2.59 (q, J = 8.0 Hz, 4H), 1.17 (t, J = 8.0 Hz, 6H). 306 CF.sub.3 [00382]embedded image (500 MHz, Chloroform-d) δ 8.66 (s, 1H), 8.51 (d, J = 5.0 Hz, 1H), 7.48 (d, J = 5.0 Hz, 1H), 7.42 (s, 1H), 6.07 (s, 1H), 3.28 (s, 2H), 2.34 (s, 6H). 307 CF.sub.3 [00383]embedded image (500 MHz, Chloroform-d) δ 8.72 (d, J = 1.5 Hz, 1H), 8.66 (d, J = 1.0 Hz, 1H), 8.12 (dd, J = 1.5, 1.0 Hz, 1H), 7.29 (s, 1H), 5.54 (s, 1H), 3.84 (s, 3H), 3.70 (s, 2H). 308 CF.sub.3 [00384]embedded image (500 MHz, Chloroform-d) δ 8.63 (d, J = 5.0 Hz, 1H), 7.79 (d, J = 1.0 Hz, 1H), 7.38 (dd, J = 5.0, 1.0 Hz, 1H), 7.12 (s, 1H), 3.69 (s, 3H), 3.59 (s, 2H). 309 CF.sub.3 [00385]embedded image (500 MHz, Chloroform-d) δ 8.67 (d, J = 5.0 Hz, 1H), 7.88 (d, J = 1.0 Hz, 1H), 7.64 (dd, J = 5.0, 1.0 Hz, 1H), 7.30 (s, 1H), 5.67 (s, 2H), 5.33 (s, 1H), 2.69 (hept, J = 6.5 Hz, 1H), 1.24 (d, J = 6.5 Hz, 6H). 310 CF.sub.3 [00386]embedded image 311 CF.sub.3 [00387]embedded image (500 MHz, Chloroform-d) δ 8.60 (d, J = 5.0 Hz, 1H), 7.99 (d, J = 1.0 Hz, 1H), 7.28 (dd, J = 5.0, 1.0 Hz, 1H), 7.14 (s, 1H), 6.87 (dd, J = 2.0, 1.0 Hz, 1H), 6.72- 6.56 (m, 3H), 4.48 (s, 1H), 3.95 (q, J = 8.0 Hz, 2H), 2.78 (s, 3H), 1.91-1.81 (m, 1H), 1.20 (t, J = 8.0 Hz, 3H), 1.14- 1.05 (m, 2H), 0.78-0.69 (m, 2H). 312 CF.sub.3 [00388]embedded image (500 MHz, Chloroform-d) δ 8.41 (d, J = 5.0 Hz, 1H), 8.23 (s, 1H), 7.59 (d, J = 5.0 Hz, 1H), 7.29 (s, 1H), 6.11 (s, 1H), 4.31 (s, 2H), 3.39 (s, 3H). 313 CF.sub.3 [00389]embedded image (500 MHz, Chloroform-d) δ 8.60 (d, J = 1.5 Hz, 1H), 8.12 (d, J = 1.0 Hz, 1H), 7.53 (dd, J = 1.5, 1.0 Hz, 1H), 7.24 (s, 1H), 5.81 (s, 1H), 4.22 (t, J = 6.5 Hz, 2H), 2.87 (t, J = 6.5 Hz, 2H), 2.12 (s, 3H). 314 CF.sub.3 [00390]embedded image 315 CF.sub.3 [00391]embedded image (500 MHz, Chloroform-d) δ 8.42 (s, 1H), 7.29 (s, 1H), 6.94 (s, 1H), 5.78 (s, 1H), 4.21 (t, J = 7.0 Hz, 2H), 2.65 (t, J = 7.0 Hz, 2H). 316 CF.sub.3 [00392]embedded image (500 MHz, Chloroform-d) δ 9.74 (d, J = 1.0 Hz, 1H), 7.93-7.84 (m, 2H), 7.22 (d, J = 2.5 Hz, 1H), 7.13 (s, 1H), 6.63 (d, J = 2.5 Hz, 1H), 4.91 (s, 2H), 3.85 (s, 3H), 3.63 (s, 2H). 317 CF.sub.3 [00393]embedded image (500 MHz, Chloroform-d) δ 7.25 (s, 1H), 7.13 (s, 1H), 5.46 (s, 2H), 3.89 (hept, J = 6.5 Hz, 1H), 3.63 (s, 2H), 3.42 (q, J = 8.0 Hz, 2H), 2.66 (s, 3H), 1.20 (t, J = 8.0 Hz, 3H), 1.15 (d, J = 6.5 Hz, 6H). 318 CF.sub.3 [00394]embedded image (500 MHz, Chloroform-d) δ 9.26 (s, 1H), 8.37 (d, J = 8.0 Hz, 1H), 8.12 (d, J = 8.0 Hz, 1H), 7.31 (s, 1H), 5.33 (s, 1H), 3.48 (q, J = 8.0 Hz, 2H), 3.21-3.13 (m, 1H), 1.97-1.87 (m, 2H), 1.84-1.72 (m, 1H), 1.75-1.57 (m, 4H), 1.54- 1.42 (m, 2H), 1.45-1.37 (m, 1H), 1.23 (t, J = 8.0 Hz, 3H). 319 CF.sub.3 [00395]embedded image (500 MHz, Chloroform-d) δ 8.01 (s, 1H), 7.33 (s, 1H), 7.34-7.23 (m, 6H), 7.07 (s, 1H), 5.83 (s, 1H), 4.88 (s, 2H). 320 CF.sub.3 [00396]embedded image (500 MHz, Chloroform-d) δ 9.45 (d, J = 1.5 Hz, 1H), 8.59 (s, 1H), 8.52 (d, J = 1.5 Hz, 1H), 7.96-7.80 (m, 2H), 7.41- 7.34 (m, 4H), 7.31-7.26 (m, 2H), 4.59 (s, 1H). 321 CF.sub.3 [00397]embedded image (500 MHz, Chloroform-d) δ 7.68 (dd, J = 2.0, 1.5 Hz, 1H), 7.17 (s, 1H), 7.07 (s, 1H), 7.01 (dd, J = 1.5, 1.0 Hz, 1H), 6.94 (dd, J = 2.0, 1.0 Hz, 1H), 4.67 (s, 1H), 3.81 (s, 3H), 3.74 (s, 3H), 2.84 (s, 3H). 322 CF.sub.3 [00398]embedded image (500 MHz, Chloroform-d) δ 9.41 (d, J = 1.0 Hz, 1H), 8.68 (d, J = 1.0 Hz, 1H), 8.03 (s, 1H), 7.44 (d, J = 2.5 Hz, 1H), 7.36-7.30 (m, 2H), 6.61 (dd, J = 2.5, 2.0 Hz, 1H), 5.82 (s, 2H), 5.17 (s, 1H), 3.63 (s, 2H). 323 CF.sub.3 [00399]embedded image (500 MHz, Chloroform-d) δ 9.07 (d, J = 1.5 Hz, 1H), 8.38 (d, J = 8.0 Hz, 1H), 8.16 (dd, J = 8.0, 1.5 Hz, 1H), 7.30 (s, 1H), 6.64 (s, 1H), 5.29 (s, 1H), 5.32- 5.20 (hept, J = 6.5 Hz, 1H), 1.29 (d, J = 6.5 Hz, 6H). 324 CF.sub.3 [00400]embedded image (500 MHz, Chloroform-d) δ 8.74 (d, J = 1.0 Hz, 1H), 8.00 (d, J = 8.0 Hz, 1H), 7.92 (dd, J = 8.0, 1.0 Hz, 1H), 7.12 (s, 1H), 5.39 (s, 1H), 3.53 (s, 3H). 325 CF.sub.3 [00401]embedded image (500 MHz, Chloroform-d) δ 8.27 (d, J = 1.0 Hz, 1H), 7.87 (d, J = 1.0 Hz, 1H), 7.31 (s, 1H), 5.43 (s, 1H), 2.68 (s, 3H), 2.32-2.21 (m, 1H), 1.37-1.27 (m, 2H), 1.08-0.99 (m, 2H). 326 CF.sub.3 [00402]embedded image (500 MHz, Chloroform-d) δ 8.07 (s, 1H), 7.84 (s, 1H), 7.13 (s, 1H), 5.33 (s, 1H), 3.58 (s, 3H), 2.70 (s, 3H). 327 CF.sub.3 [00403]embedded image (500 MHz, Chloroform-d) δ 9.32 (s, 1H), 8.82 (d, J = 5.5 Hz, 1H), 8.76 (d, J = 5.5 Hz, 1H), 7.10 (s, 1H), 5.13 (s, 1H). 328 CF.sub.3 [00404]embedded image (500 MHz, Chloroform-d) δ 9.24 (s, 1H), 8.72 (s, 1H), 7.29 (s, 1H), 5.18 (s, 1H). 329 CF.sub.3 [00405]embedded image (500 MHz, Chloroform-d) δ 9.42 (s, 1H), 9.11 (s, 1H), 7.30 (s, 1H), 5.23 (s, 1H). 330 CF.sub.3 [00406]embedded image (500 MHz, Chloroform-d) δ 8.62 (d, J = 5.5 Hz, 1H), 8.34 (d, J = 5.5 Hz, 1H), 7.28 (s, 1H), 5.19 (s, 1H), 2.80 (s, 3H). 331 CF.sub.3 [00407]embedded image (500 MHz, Chloroform-d) δ 9.18 (s, 1H), 7.31 (s, 1H), 6.93 (s, 1H), 5.43 (s, 1H), 1.99-1.83 (m, 1H), 0.91-0.81 (m, 2H), 0.70-0.60 (m, 2H). 332 CF.sub.3 [00408]embedded image (500 MHz, Chloroform-d) δ 9.91 (s, 1H), 7.35 (s, 1H), 6.96-6.82 (m, 1H), 6.01-5.83 (m, 1H), 5.35 (s, 1H). 333 CF.sub.3 [00409]embedded image (500 MHz, Chloroform-d) δ 8.12 (s, 1H), 7.99 (s, 1H), 7.28 (s, 1H), 5.29 (s, 1H). 334 CF.sub.3 [00410]embedded image (500 MHz, Chloroform-d) δ 9.13 (s, 1H), 8.40 (s, 1H), 7.28 (s, 1H), 5.39 (s, 1H), 4.89 (hept, J = 6.5 Hz, 1H), 1.30 (d, J = 6.5 Hz, 6H). 335 CF.sub.3 [00411]embedded image (500 MHz, Chloroform-d) δ 8.35 (s, 1H), 7.25 (s, 1H), 5.91-5.80 (m, 1H), 5.70 (s, 1H), 4.34-4.28 (m, 2H). 336 CF.sub.3 [00412]embedded image 337 CF.sub.3 [00413]embedded image (500 MHz, Chloroform-d) δ 7.26 (s, 1H), 5.71 (s, 1H), 3.35 (s, 3H). 338 CF.sub.3 [00414]embedded image (500 MHz, Chloroform-d) δ 9.21 (s, 1H), 8.55 (s, 1H), 7.33 (s, 1H), 5.07 (s, 1H), 3.53 (q, J = 8.0 Hz, 2H), 2.97 (q, J = 8.0 Hz, 2H), 1.37 (t, J = 8.0 Hz, 3H), 1.20 (t, J = 8.0 Hz, 3H). 339 CF.sub.3 [00415]embedded image (500 MHz, Chloroform-d) δ 9.34 (s, 1H), 8.75 (s, 1H), 7.30-7.23 (m, 2H), 7.02-6.96 (m, 3H), 5.41 (s, 1H), 3.88 (s, 2H), 3.71 (s, 3H). 340 CF.sub.3 [00416]embedded image 341 CF.sub.3 [00417]embedded image (500 MHz, Chloroform-d) δ 9.50 (dd, J = 5.5, 1.5 Hz, 1H), 8.01 (dd, J = 7.5, 1.5 Hz, 1H), 7.82 (dd, J = 7.5, 5.5 Hz, 1H), 7.23 (s, 1H), 5.77 (s, 1H). 342 CF.sub.3 [00418]embedded image (500 MHz, Chloroform-d) δ 9.49 (d, J = 5.5 Hz, 1H), 7.88 (d, J = 5.5 Hz, 1H), 7.29 (s, 1H), 5.37 (s, 1H). 343 CF.sub.3 [00419]embedded image (500 MHz, Chloroform-d) δ 8.78 (d, J = 7.5 Hz, 1H), 8.38 (d, J = 7.5 Hz, 1H), 7.24 (s, 1H), 5.82 (s, 1H). 344 CF.sub.3 [00420]embedded image (500 MHz, Chloroform-d) δ 9.40 (d, J = 1.5 Hz, 1H), 7.94 (d, J = 1.5 Hz, 1H), 7.27 (s, 1H), 5.62 (s, 1H), 2.60 (t, J = 8.0 Hz, 2H), 1.54-1.31 (m, 4H), 0.89 (t, J = 7.5 Hz, 3H). 345 CF.sub.3 [00421]embedded image (500 MHz, Chloroform-d) δ 7.96 (d, J = 7.5 Hz, 1H), 7.77 (d, J = 7.5 Hz, 1H), 7.23 (s, 1H), 5.79 (s, 1H), 4.33-4.12 (m, 2H), 3.17-3.01 (m, 1H), 2.12- 1.88 (m, 2H), 1.39 (d, J = 6.5 Hz, 3H). 346 CF.sub.3 [00422]embedded image (500 MHz, Chloroform-d) δ 8.02 (d, J = 7.5 Hz, 1H), 7.69 (d, J = 7.5 Hz, 1H), 7.27 (s, 1H), 5.39 (s, 1H), 4.46-4.23 (m, 1H), 2.53-2.34 (m, 1H), 1.53- 1.29 (m, 1H). 347 CF.sub.3 [00423]embedded image (500 MHz, Chloroform-d) δ 9.31 (d, J = 1.5 Hz, 1H), 7.46 (d, J = 1.5 Hz, 1H), 7.25 (s, 1H), 5.93 (s, 1H), 5.49 (s, 1H). 348 CF.sub.3 [00424]embedded image (500 MHz, Chloroform-d) δ 7.99 (d, J = 7.5 Hz, 1H), 7.86 (d, J = 7.5 Hz, 1H), 7.27 (s, 1H), 5.63 (s, 1H), 5.17 (s, 1H). 349 CF.sub.3 [00425]embedded image (500 MHz, Chloroform-d) δ 8.04 (d, J = 7.5 Hz, 1H), 7.98 (d, J = 7.3 Hz, 1H), 7.26 (s, 1H), 5.44 (s, 1H), 3.35 (s, 1H). 350 CF.sub.3 [00426]embedded image 351 CF.sub.3 [00427]embedded image (500 MHz, Chloroform-d) δ 8.30 (s, 1H), 7.84 (s, 1H), 7.31 (s, 1H), 5.53 (s, 1H). 352 CF.sub.3 [00428]embedded image (500 MHz, Chloroform-d) δ 9.58 (s, 1H), 7.07 (s, 1H), 5.31 (s, 1H), 3.73 (s, 3H). 353 CF.sub.3 [00429]embedded image (500 MHz, Chloroform-d) δ 7.23 (s, 1H), 7.07 (s, 1H), 5.98-5.81 (m, 1H), 5.77 (s, 1H), 5.29-5.20 (m, 1H), 5.14- 5.03 (m, 1H), 4.90 (s, 1H), 3.99-3.83 (m, 2H), 3.76 (s, 3H). 354 CF.sub.3 [00430]embedded image 355 CF.sub.3 [00431]embedded image (500 MHz, Chloroform-d) δ 8.12 (d, J = 7.5 Hz, 1H), 7.48 (d, J = 7.5 Hz, 1H), 7.30-7.17 (m, 4H), 7.33 (s, 1H), 5.41 (s, 1H). 356 CF.sub.3 [00432]embedded image (500 MHz, Chloroform-d) δ 7.86 (d, J = 7.5 Hz, 1H), 7.28 (s, 1H), 7.06 (d, J = 7.5 Hz, 1H), 5.21 (s, 1H), 2.86 (s, 3H), 2.27 (q, J = 8.0 Hz, 2H), 1.12 (t, J = 8.0 Hz, 3H). 357 CF.sub.3 [00433]embedded image (500 MHz, Chloroform-d) δ 8.02 (d, J = 7.5 Hz, 1H), 7.85 (d, J = 7.5 Hz, 1H), 7.27 (s, 1H), 5.46 (s, 1H), 2.97 (q, J = 8.1 Hz, 2H), 1.37 (t, J = 8.0 Hz, 3H). 358 CF.sub.3 [00434]embedded image (500 MHz, Chloroform-d) δ 9.72 (d, J = 1.5 Hz, 1H), 9.43 (d, J = 5.5 Hz, 1H), 8.04 (dd, J = 5.5, 1.5 Hz, 1H), 7.24 (s, 1H), 5.86 (s, 1H). 359 CF.sub.3 [00435]embedded image (500 MHz, Chloroform-d) δ 8.61 (d, J = 1.5 Hz, 1H), 8.21 (d, J = 1.5 Hz, 1H), 7.26 (s, 1H), 5.87 (s, 1H). 360 CF.sub.3 [00436]embedded image (500 MHz, Chloroform-d) δ 9.48 (s, 1H), 9.42 (s, 1H), 7.27 (s, 1H), 5.60 (s, 1H), 2.36 (s, 3H). 361 CF.sub.3 [00437]embedded image (500 MHz, Chloroform-d) δ 9.58 (d, J = 1.5 Hz, 1H), 7.94 (d, J = 1.5 Hz, 1H), 7.28 (s, 1H), 5.54 (s, 1H), 4.47-4.37 (m, 2H), 2.75-2.34 (m, 2H). 362 CF.sub.3 [00438]embedded image (500 MHz, Chloroform-d) δ 9.35 (d, J = 6.0 Hz, 1H), 7.84 (d, J = 6.0 Hz, 1H), 7.27 (s, 1H), 5.73 (s, 1H), 2.38-2.22 (m, 1H), 0.85-0.74 (m, 2H), 0.73- 0.61 (m, 2H). 363 CF.sub.3 [00439]embedded image (500 MHz, Chloroform-d) δ 7.90 (s, 1H), 7.27 (s, 1H), 6.39-6.29 (m, 2H), 5.61 (s, 1H), 2.76 (s, 3H), 2.16 (d, J = 6.0 Hz, 3H). 364 CF.sub.3 [00440]embedded image (500 MHz, Chloroform-d) δ 7.99 (s, 1H), 7.72 (s, 1H), 7.37 (s, 1H), 5.37 (s, 1H). 365 CF.sub.3 [00441]embedded image (500 MHz, Chloroform-d) δ 7.57 (s, 1H), 6.95 (s, 1H). 366 CF.sub.3 [00442]embedded image (500 MHz, Chloroform-d) δ 9.53 (d, J = 1.5 Hz, 1H), 8.08 (d, J = 1.5 Hz, 1H), 7.24 (s, 1H), 5.86 (s, 1H), 3.78 (t, J = 7.5 Hz, 2H), 3.21 (t, J = 7.5 Hz, 2H). 367 CF.sub.3 [00443]embedded image (500 MHz, Chloroform-d) δ 9.63 (d, J = 1.5 Hz, 1H), 8.02 (d, J = 1.5 Hz, 1H), 7.46-7.29 (m, 3H), 7.23 (s, 1H), 5.80 (s, 1H), 3.88 (s, 2H). 368 CF.sub.3 [00444]embedded image (500 MHz, Chloroform-d) δ 8.03 (s, 1H), 7.37 (s, 1H), 6.50 (s, 1H), 3.27 (s, 6H), 2.97 (q, J = 8.0 Hz, 2H), 1.36 (t, J = 8.0 Hz, 3H). 369 CF.sub.3 [00445]embedded image (500 MHz, Chloroform-d) δ 9.95 (s, 1H), 7.26 (s, 1H), 5.43 (s, 1H), 4.34 (q, J = 8.0 Hz, 2H), 3.39 (s, 3H), 1.61 (t, J = 8.0 Hz, 3H). 370 CF.sub.3 [00446]embedded image (500 MHz, Chloroform-d) δ 8.27-8.06 (m, 2H), 8.04-7.94 (m, 2H), 7.84- 7.70 (m, 1H), 7.55-7.50 (m, 2H), 7.09 (s, 1H), 5.52 (s, 1H). 371 CF.sub.3 [00447]embedded image (500 MHz, Chloroform-d) δ 8.23-7.96 (m, 2H), 7.82-7.71 (m, 3H), 7.62- 6.51 (m, 1H), 7.09 (s, 1H), 5.47 (s, 1H). 372 CF.sub.3 [00448]embedded image (500 MHz, Chloroform-d) δ 8.18-7.93 (m, 2H), 7.69-7.55 (m, 2H), 7.23- 7.16 (m, 1H), 7.10 (s, 1H), 6.98-6.91 (m, 1H), 5.47 (s, 1H), 3.87 (s, 3H). 373 CF.sub.3 [00449]embedded image (500 MHz, Chloroform-d) δ 8.04-7.80 (m, 2H), 7.64-7.55 (m, 1H), 7.31- 7.26 (m, 2H), 7.14-7.09 (m, 2H), 5.52 (s, 1H), 3.87 (s, 3H). 374 CF.sub.3 [00450]embedded image (500 MHz, Chloroform-d) δ 8.76 (d, J = 1.5 Hz, 1H), 8.34-8.25 (m, 2H), 8.10- 7.90 (m, 2H), 7.05 (s, 1H), 6.77-6.51 (m, 1H), 5.76-5.65 (m, 2H), 5.25- 5.11 (m, 1H), 3.16 (s, 3H). 375 CF.sub.3 [00451]embedded image (500 MHz, Chloroform-d) δ 8.24-8.19 (m, 2H), 8.12 (d, J = 1.5 Hz, 1H), 7.87- 7.63 (m, 2H), 7.11 (s, 1H), 5.33 (s, 1H), 3.95 (s, 3H). 376 CF.sub.3 [00452]embedded image (500 MHz, Chloroform-d) δ 8.21-8.16 (m, 1H), 7.94-7.85 (m, 1H), 7.77- 7.55 (m, 2H), 7.42-7.31 (m, 2H), 7.09 (s, 1H), 5.52 (s, 1H), 1.94-1.82 (m, 1H), 1.23-1.14 (m, 2H), 0.96-0.87 (m, 2H). 377 CF.sub.3 [00453]embedded image (500 MHz, Chloroform-d) δ 8.63-8.51 (m, 1H), 8.06-7.99 (m, 2H), 7.90- 7.84 (m, 1H), 7.81-7.76 (m, 2H), 7.07 (s, 1H), 6.11 (s, 1H), 2.65 (s, 3H). 378 CF.sub.3 [00454]embedded image (500 MHz, Chloroform-d) δ 9.50 (s, 1H), 7.99-7.90 (m, 2H), 7.89-7.81 (m, 1H), 7.67-7.47 (m, 3H), 7.03 (s, 1H), 5.43 (s, 1H), 2.22 (s, 3H). 379 CF.sub.3 [00455]embedded image (500 MHz, Chloroform-d) δ 8.20-7.95 (m, 2H), 7.87-7.81 (m, 1H), 7.78- 7.64 (m, 3H), 7.10 (s, 1H), 5.48 (s, 1H), 3.78 (t, J = 7.5 Hz, 2H), 3.07 (t, J = 7.5 Hz, 2H). 380 CF.sub.3 [00456]embedded image (500 MHz, Chloroform-d) δ 8.11-8.01 (m, 2H), 7.99-7.87 (m, 1H), 7.92- 7.78 (m, 2H), 7.53-7.47 (m, 2H), 7.09 (s, 1H), 5.63 (s, 1H). 381 CF.sub.3 [00457]embedded image (500 MHz, Chloroform-d) δ 7.79-7.57 (m, 3H), 7.56 (d, J = 1.5 Hz, 1H), 7.20- 7.13 (m, 2H), 7.08 (s, 1H), 5.55 (s, 1H), 5.00 (s, 1H), 2.82 (s, 3H). 382 CF.sub.3 [00458]embedded image (500 MHz, Chloroform-d) δ 8.11-8.02 (m, 2H), 8.00-7.90 (m, 2H), 7.78- 7.65 (m, 2H), 7.50 (t, J = 73.5 Hz, 2H), 7.09 (s, 1H), 5.55 (s, 1H). 383 CF.sub.3 [00459]embedded image (500 MHz, Chloroform-d) δ 8.03-7.93 (m, 2H), 7.92-7.83 (m, 2H), 7.46- 7.38 (m, 2H), 7.09 (s, 1H), 5.61 (s, 1H), 2.50 (s, 3H). 384 CF.sub.3 [00460]embedded image (500 MHz, Chloroform-d) δ 8.13-8.02 (m, 2H), 7.89-7.77 (m, 2H), 7.65- 7.52 (m, 2H), 7.10 (s, 1H), 5.51 (s, 1H). 385 CF.sub.3 [00461]embedded image (500 MHz, Chloroform-d) δ 8.12-8.04 (m, 2H), 7.87-7.62 (d, J = 8.0 Hz, 4H), 7.07 (s, 1H), 5.26 (s, 1H). 386 CF.sub.3 [00462]embedded image (500 MHz, Chloroform-d) δ 8.57 (d, J = 1.5 Hz, 1H), 8.10-8.02 (m, 3H), 7.99- 7.81 (m, 2H), 7.09 (s, 1H), 6.26 (d, J = 72.5 Hz 1H), 5.53 (s, 1H). 387 CF.sub.3 [00463]embedded image (500 MHz, Chloroform-d) δ 8.33-8.23 (m, 2H), 8.09-7.98 (m, 2H), 7.10 (s, 1H), 6.34-6.22 (m, 1H), 5.50 (s, 1H), 3.95 (s, 3H), 3.90 (s, 3H). 388 CF.sub.3 [00464]embedded image (500 MHz, Chloroform-d) δ 8.11-8.00 (m, 2H), 7.91-7.78 (m, 2H), 7.47- 7.37 (m, 2H), 7.05 (s, 1H), 5.51 (s, 1H), 3.51 (t, J = 7.5 Hz, 2H), 3.23 (s, 3H), 2.43 (t, J = 7.5 Hz, 2H). 389 CF.sub.3 [00465]embedded image (500 MHz, Chloroform-d) δ 8.15-8.03 (m, 1H), 7.87-7.78 (m, 2H), 7.61- 7.44 (m, 2H), 7.10-7.01 (m, 2H), 6.12 (s, 2H), 5.52 (s, 1H), 3.29 (s, 3H). 390 CF.sub.3 [00466]embedded image (500 MHz, Chloroform-d) δ 8.42 (s, 1H), 8.27 (d, J = 1.5 Hz, 1H), 7.92 (d, J = 7.5 Hz, 1H), 7.50 (dd, J = 7.5, 1.5 Hz, 1H), 7.04 (s, 1H), 5.63 (s, 1H), 3.18 (s, 3H), 3.03-2.98 (m, 2H), 2.68 (s, 3H), 2.16-2.06 (m, 1H), 1.44-1.33 (m, 1H), 0.99-0.84 (m, 2H). 391 CF.sub.3 [00467]embedded image 392 CF.sub.3 [00468]embedded image (500 MHz, Chloroform-d) δ 8.31 (d, J = 7.5 Hz, 1H), 8.10 (d, J = 7.5 Hz, 1H), 7.84-7.70 (m, 3H), 7.54-7.42 (m, 1H), 7.09 (s, 1H), 5.63 (s, 1H), 3.70 (s, 2H), 2.27 (s, 3H). 393 CF.sub.3 [00469]embedded image (500 MHz, Chloroform-d) δ 7.82-7.73 (m, 1H), 7.67-7.60 (m, 2H), 7.19 (d, J = 1.5 Hz, 1H), 7.07 (s, 1H), 5.40 (s, 1H), 3.81 (s, 2H), 2.52 (s, 3H), 2.35 (s, 3H), 2.27 (s, 3H). 394 CF.sub.3 [00470]embedded image (500 MHz, Chloroform-d) δ 8.30-8.13 (m, 2H), 7.85-7.76 (m, 2H), 7.69- 7.62 (m, 2H), 7.09 (s, 1H), 5.43 (s, 1H), 4.53 (s, 2H), 3.95 (s, 2H), 3.28 (s, 3H). 395 CF.sub.3 [00471]embedded image (500 MHz, Chloroform-d) δ 8.42-8.37 (m, 1H), 7.54 (d, J = 1.5 Hz, 1H), 7.47- 7.36 (m, 2H), 7.04 (s, 1H), 6.88-6.69 (m, 1H), 5.71 (s, 1H), 4.96 (s, 2H), 3.90 (s, 3H). 396 CF.sub.3 [00472]embedded image (500 MHz, Chloroform-d) δ 8.38 (d, J = 1.5 Hz, 1H), 8.18 (dd, J = 7.5, 1.5 Hz, 1H), 8.12-8.01 (m, 2H), 7.88-7.62 (m, 2H), 7.07 (s, 1H), 5.55 (s, 1H), 2.42 (s, 3H). 397 CF.sub.3 [00473]embedded image (500 MHz, Chloroform-d) δ 8.05-7.97 (m, 1H), 8.00-7.91 (m, 2H), 7.76- 7.68 (m, 2H), 7.58-7.42 (m, 1H), 7.08 (s, 1H), 5.57 (s, 1H), 3.82 (s, 2H), 1.85 (s, 3H). 398 CF.sub.3 [00474]embedded image (500 MHz, Chloroform-d) δ 7.99-7.93 (m, 2H), 7.83-7.53 (m, 2H), 7.40- 7.24 (m, 2H), 7.09 (s, 1H), 5.49 (d, J = 73.5 Hz, 1H), 5.20 (s, 1H). 399 CF.sub.3 [00475]embedded image 400 CF.sub.3 [00476]embedded image (500 MHz, Chloroform-d) δ 8.43-8.34 (m, 2H), 7.99-7.82 (m, 2H), 7.73- 7.66 (m, 1H), 7.09 (s, 1H), 6.24-6.12 (m, 1H), 5.57 (s, 1H), 5.10 (s, 2H), 2.20 (s, 3H). 401 CF.sub.3 [00477]embedded image (500 MHz, Chloroform-d) δ 8.00-7.88 (m, 2H), 7.91-7.70 (m, 2H), 7.51- 7.39 (m, 1H), 7.11-7.05 (m, 2H), 5.62 (s, 1H), 4.93 (s, 2H), 3.73 (s, 3H). 402 CF.sub.3 [00478]embedded image (500 MHz, Chloroform-d) δ 8.69-8.42 (m, 2H), 8.11-8.00 (m, 2H), 7.78- 7.53 (m, 2H), 7.50-7.42 (m, 2H), 7.12- 7.03 (m, 3H), 5.71 (s, 1H), 3.94 (hept, J = 6.5 Hz, 1H), 1.52 (d, J = 6.5 Hz, 6H). 403 CF.sub.3 [00479]embedded image (500 MHz, Chloroform-d) δ 8.71-8.63 (m, 1H), 8.34-8.20 (m, 2H), 8.13- 8.04 (m, 2H), 7.88-7.79 (m, 1H), 7.10 (s, 1H), 5.72-5.50 (m, 1H), 5.44 (s, 1H), 4.48 (s, 2H), 2.72-2.50 (m, 2H), 2.39 (s, 3H). 404 CF.sub.3 [00480]embedded image (500 MHz, Chloroform-d) δ 8.11-8.06 (m, 2H), 7.73-7.64 (m, 2H), 7.51- 7.37 (m, 2H), 7.09 (s, 1H), 5.61 (s, 1H), 4.48 (s, 2H), 3.34 (s, 3H). 405 CF.sub.3 [00481]embedded image 406 CF.sub.3 [00482]embedded image (500 MHz, Chloroform-d) δ 8.06 (s, 1H), 7.74-7.64 (m, 2H), 7.42-7.29 (m, 2H), 7.09 (s, 1H), 5.64 (s, 1H), 5.24 (s, 2H), 5.00 (s, 2H), 4.27 (s, 2H), 3.70 (hept, J = 6.5 Hz, 1H), 3.10 (q, J = 8.0 Hz, 2H), 1.35 (t, J = 8.0 Hz, 3H), 1.02 (d, J = 6.5 Hz, 6H). 407 CF.sub.3 [00483]embedded image (500 MHz, Chloroform-d) δ 8.05-7.98 (m, 2H), 7.79-7.72 (m, 2H), 7.50- 7.43 (m, 2H), 7.31 (s, 1H), 5.41 (s, 1H), 5.11 (s, 2H), 2.86 (s, 3H). 408 CF.sub.3 [00484]embedded image (500 MHz, Chloroform-d) δ 7.88 (d, J = 7.5 Hz, 1H), 7.72-7.64 (m, 2H), 7.63 (d, J = 7.5 Hz, 1H), 7.56 (d, J = 7.5 Hz, 1H), 7.09 (s, 1H), 5.51 (s, 1H), 3.81 (s, 2H), 3.64-3.47 (m, 1H), 2.94 (s, 3H), 1.83-1.71 (m, 3H), 1.71-1.57 (m, 2H), 1.57-1.37 (m, 5H). 409 CF.sub.3 [00485]embedded image (500 MHz, Chloroform-d) δ 7.68-7.55 (m, 2H), 7.41-7.31 (m, 3H), 7.28- 7.19 (m, 1H), 7.09 (s, 1H), 6.06 (s, 2H), 5.55 (s, 1H), 3.45 (q, J = 8.0 Hz, 2H), 1.22 (t, J = 8.0 Hz, 3H). 410 CF.sub.3 [00486]embedded image (500 MHz, Chloroform-d) δ 8.10-8.00 (m, 2H), 7.94-7.81 (m, 1H), 7.79- 7.65 (m, 2H), 7.49-7.33 (m, 1H), 7.09 (s, 1H), 5.56 (s, 1H), 5.11 (s, 2H), 4.67 (s, 2H), 2.59 (q, J = 8.0 Hz, 2H), 1.29 (s, 1H), 1.02 (t, J = 8.0 Hz, 3H). 411 CF.sub.3 [00487]embedded image 412 CF.sub.3 [00488]embedded image (500 MHz, Chloroform-d) δ 8.18 (d, J = 1.5 Hz, 1H), 8.02 (dd, J = 7.5, 1.5 Hz, 1H), 7.85-7.77 (m, 2H), 7.53-7.43 (m, 2H), 7.10 (s, 1H), 5.41 (s, 1H), 4.27 (s, 2H), 2.56 (s, 3H). 413 CF.sub.3 [00489]embedded image (500 MHz, Chloroform-d) δ 7.83 (dd, J = 2.5 Hz, 1H), 7.17 (d, J = 2.0 Hz, 2H), 6.80 (dd, J = 2.5, 2.0 Hz, 1H). 414 CF.sub.3 [00490]embedded image (500 MHz, Chloroform-d) δ 7.18 (s, 1H), 6.90 (d, J = 2.5 Hz, 1H), 6.11 (d, J = 2.5 Hz, 1H), 2.36 (s, 3H). 415 CF.sub.3 [00491]embedded image (500 MHz, Chloroform-d) δ 7.40 (s, 1H), 7.20 (s, 1H), 6.30 (s, 1H), 6.00 (s, 1H), 2.94 (hept, J = 6.5 Hz, 1H), 1.52 (d, J = 6.5 Hz, 6H). 416 CF.sub.3 [00492]embedded image (500 MHz, Chloroform-d) δ 7.35 (d, J = 2.5 Hz, 1H), 7.18 (s, 1H), 6.45 (d, J = 2.5 Hz, 1H), 2.66 (q, J = 8.0 Hz, 2H), 1.30 (t, J = 8.0 Hz, 3H). 417 CF.sub.3 [00493]embedded image (500 MHz, Chloroform-d) δ 7.40 (d, J = 9.0 Hz, 1H), 7.20 (s, 1H), 6.30 (d, J = 8.5 Hz, 1H), 6.00 (s, 1H). 418 CF.sub.3 [00494]embedded image (500 MHz, Chloroform-d) δ 7.50 (s, 1H), 7.18 (s, 1H), 6.67 (s, 1H), 5.64 (s, 1H). 419 CF.sub.3 [00495]embedded image (500 MHz, Chloroform-d) δ 7.45 (d, J = 2.5 Hz, 1H), 7.15 (s, 1H), 6.76 (d, J = 2.5 Hz, 1H), 5.84 (s, 1H). 420 CF.sub.3 [00496]embedded image (500 MHz, Chloroform-d) δ 7.18 (s, 1H), 6.85 (d, J = 2.5 Hz, 1H), 5.80 (d, J = 2.5 Hz, 1H), 3.85 (s, 3H). 421 CF.sub.3 [00497]embedded image (500 MHz, Chloroform-d) δ 7.29 (d, J = 2.5 Hz, 1H), 7.20 (s, 1H), 7.06 (d, J = 2.5 Hz, 1H), 5.67 (s, 1H). 422 CF.sub.3 [00498]embedded image (500 MHz, Chloroform-d) δ 7.43 (d, J = 2.5 Hz, 1H), 7.30 (d, J = 2.5 Hz, 1H), 7.17 (s, 1H), 5.77 (s, 1H). 423 CF.sub.3 [00499]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 10.38 (s, 1H), 7.71 (d, J = 1.5 Hz, 1H), 7.47 (d, J = 1.5 Hz, 1H), 7.13 (s, 1H), 6.43 (s, 1H). 424 CF.sub.3 [00500]embedded image (500 MHz, Chloroform-d) δ 7.20 (d, J = 2.5 Hz, 1H), 7.15 (s, 1H), 6.42 (d, J = 2.5 Hz, 1H), 5.81 (s, 1H), 2.37 (s, 3H). 425 CF.sub.3 [00501]embedded image (500 MHz, Chloroform-d) δ 7.63 (s, 1H), 7.15 (s, 1H), 6.09 (s, 1H), 5.87 (s, 1H), 2.38 (t, J = 6.5 Hz, 2H), 1.86- 1.71 (m, 2H), 1.00 (t, J = 8.0 Hz, 3H). 426 CF.sub.3 [00502]embedded image (500 MHz, Chloroform-d) δ 7.34 (s, 1H), 7.27 (s, 1H), 7.20 (s, 1H), 6.07 (s, 1H), 1.30 (s, 9H). 427 CF.sub.3 [00503]embedded image (500 MHz, Chloroform-d) δ 7.30 (d, J = 2.5 Hz, 1H), 7.16 (s, 1H), 6.32 (d, J = 2.5 Hz, 1H), 5.74 (s, 1H). 428 CF.sub.3 [00504]embedded image (500 MHz, Chloroform-d) δ 7.40 (s, 1H), 7.20 (s, 1H), 6.30 (d, J = 8.0 Hz, 1H), 6.00 (s, 1H). 429 CF.sub.3 [00505]embedded image (500 MHz, Chloroform-d) δ 7.60 (s, 1H), 7.53 (s, 1H), 7.24 (s, 1H), 5.52 (s, 1H). 430 CF.sub.3 [00506]embedded image (500 MHz, Chloroform-d) δ 8.99 (s, 1H), 8.25 (s, 1H), 7.20 (s, 1H), 6.90 (d, J = 7.5 Hz, 1H), 6.11 (d, J = 7.5 Hz, 1H), 2.87 (s, 3H). 431 CF.sub.3 [00507]embedded image (500 MHz, Chloroform-d) δ 7.59 (s, 1H), 7.15 (s, 1H), 6.40 (s, 1H), 5.88 (s, 1H), 2.43 (s, 3H). 432 CF.sub.3 [00508]embedded image (500 MHz, Chloroform-d) δ 7.24 (s, 1H), 7.20 (s, 1H), 7.10 (s, 1H), 6.00 (s, 1H), 1.50-1.37 (m, 1H), 1.12-1.02 (m, 2H), 0.82-0.72 (m, 2H). 433 CF.sub.3 [00509]embedded image (500 MHz, Chloroform-d) δ 7.18 (s, 1H), 6.70 (s, 1H), 6.44 (s, 1H), 5.87 (s, 1H), 5.66 (s, 1H). 434 CF.sub.3 [00510]embedded image (500 MHz, Chloroform-d) δ 8.40 (s, 1H), 7.73 (s, 1H), 7.19 (s, 1H). 435 CF.sub.3 [00511]embedded image (500 MHz, Chloroform-d) δ 7.15 (s, 1H), 6.86 (d, J = 2.5 Hz, 1H), 6.17 (d, J = 2.5 Hz, 1H). 436 CF.sub.3 [00512]embedded image (500 MHz, Chloroform-d) δ 7.29 (d, J = 2.5 Hz, 1H), 7.23-7.18 (m, 2H), 3.91 (s, 3H). 437 CF.sub.3 [00513]embedded image (500 MHz, Chloroform-d) δ 7.47 (d, J = 2.5 Hz, 1H), 7.16 (s, 1H), 6.49 (d, J = 2.5 Hz, 1H), 2.99 (s, 6H). 438 CF.sub.3 [00514]embedded image 439 CF.sub.3 [00515]embedded image (500 MHz, Chloroform-d) δ 7.17 (s, 1H), 6.04 (s, 1H), 2.36 (s, 3H), 2.26 (s, 3H). 440 CF.sub.3 [00516]embedded image (500 MHz, Chloroform-d) δ 7.56 (s, 1H), 7.18 (s, 1H), 7.06 (s, 1H), 6.83- 6.67 (m, 1H), 5.67-5.46 (m, 2H). 441 CF.sub.3 [00517]embedded image .sup.1H NMR (500 MHz, Chloroform-d) δ 7.17 (s, 1H), 6.57 (s, 1H), 5.32 (s, 1H), 2.19 (s, 3H). 442 CF.sub.3 [00518]embedded image (500 MHz, Chloroform-d) δ 7.17 (s, 1H), 2.32 (s, 3H), 2.19 (s, 3H), 2.05 (s, 3H). 443 CF.sub.3 [00519]embedded image (500 MHz, Chloroform-d) δ 7.27 (d, J = 2.5 Hz, 1H), 7.15 (s, 1H), 6.37 (d, J = 2.5 Hz, 1H), 5.78 (s, 1H), 4.48 (s, 2H), 3.38 (s, 3H). 444 CF.sub.3 [00520]embedded image (500 MHz, Chloroform-d) δ 7.27 (s, 1H), 7.15 (s, 1H), 5.78 (s, 1H), 3.88 (q, J = 8.0 Hz, 2H), 3.08 (s, 3H), 1.48 (t, J = 8.0 Hz, 3H). 445 CF.sub.3 [00521]embedded image (500 MHz, Chloroform-d) δ 7.64 (s, 1H), 7.26 (s, 1H), 7.19 (s, 1H), 6.09- 6.00 (m, 1H), 5.74 (s, 1H), 2.95-2.89 (m, 2H). 446 CF.sub.3 [00522]embedded image (500 MHz, Chloroform-d) δ 7.16 (s, 1H), 5.73 (s, 1H), 2.30 (s, 3H), 2.24 (s, 3H), 2.05 (s, 3H). 447 CF.sub.3 [00523]embedded image (500 MHz, Chloroform-d) δ 7.40 (s, 1H), 7.20 (s, 1H), 6.00 (s, 1H). 448 CF.sub.3 [00524]embedded image (500 MHz, Chloroform-d) δ 7.21 (s, 2H), 5.97 (s, 1H), 2.31 (s, 3H), 2.05 (s, 3H). 449 CF.sub.3 [00525]embedded image (500 MHz, Chloroform-d) δ 9.78 (s, 1H), 7.64 (d, J = 2.5 Hz, 1H), 7.43 (s, 1H), 6.56 (d, J = 2.5 Hz, 1H), 3.16 (s, 3H). 450 CF.sub.3 [00526]embedded image (500 MHz, Chloroform-d) δ 7.17 (s, 1H), 7.05 (s, 1H), 5.74 (s, 1H), 5.39 (s, 1H), 2.34 (s, 3H). 451 CF.sub.3 [00527]embedded image (500 MHz, Chloroform-d) δ 8.50 (s, 1H), 8.34 (s, 1H), 7.66 (s, 1H), 7.44 (s, 1H), 2.55 (s, 3H). 452 CF.sub.3 [00528]embedded image (500 MHz, Chloroform-d) δ 8.69 (s, 1H), 7.25-7.17 (m, 2H), 7.09 (d, J = 2.5 Hz, 1H). 453 CF.sub.3 [00529]embedded image (500 MHz, Chloroform-d) δ 7.99 (s, 1H), 7.50 (s, 1H), 7.21 (s, 1H), 6.41 (s, 1H), 3.01 (s, 1H). 454 CF.sub.3 [00530]embedded image (500 MHz, Chloroform-d) δ 7.56-7.44 (m, 2H), 7.24-7.17 (m, 2H). 455 CF.sub.3 [00531]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.05 (s, 1H), 7.66 (d, J = 2.5 Hz, 1H), 7.12 (d, J = 2.5 Hz, 1H), 6.88 (s, 1H), 2.40 (s, 3H). 456 CF.sub.3 [00532]embedded image (500 MHz, Chloroform-d) δ 7.46 (s, 1H), 7.20 (s, 2H), 7.09 (s, 1H), 2.30 (s, 3H). 457 CF.sub.3 [00533]embedded image (500 MHz, Chloroform-d) δ 7.46 (s, 1H), 7.19 (s, 1H), 7.09 (s, 1H), 2.71 (q, J = 8.0 Hz, 2H), 1.26 (t, J = 8.0 Hz, 3H). 458 CF.sub.3 [00534]embedded image (500 MHz, Chloroform-d) δ 7.46 (d, J = 2.5 Hz, 1H), 7.19 (s, 1H), 7.09 (d, J = 2.5 Hz, 1H), 2.71 (hept, J = 8.0 Hz, 1H), 1.26 (d, J = 8.0 Hz, 6H). 459 CF.sub.3 [00535]embedded image (500 MHz, Chloroform-d) δ 7.24 (d, J = 2.5 Hz, 1H), 7.15 (s, 1H), 6.29 (d, J = 2.5 Hz, 1H), 5.74 (s, 1H), 3.85 (s, 3H). 460 CF.sub.3 [00536]embedded image (500 MHz, Chloroform-d) δ 7.60 (s, 1H), 7.34 (s, 1H), 7.09 (s, 1H), 2.41 (s, 3H). 461 CF.sub.3 [00537]embedded image (500 MHz, Chloroform-d) δ 7.52 (d, J = 2.5 Hz, 1H), 7.33 (d, J = 2.5 Hz, 1H), 7.17 (s, 1H), 5.75 (s, 1H). 462 CF.sub.3 [00538]embedded image (500 MHz, Chloroform-d) δ 7.22-7.13 (m, 2H), 6.72-6.57 (m, 1H), 6.00 (s, 1H). 463 CF.sub.3 [00539]embedded image (500 MHz, Chloroform-d) δ 7.94 (s, 1H), 7.38 (s, 1H), 7.20 (s, 1H), 7.10 (s, 1H). 464 CF.sub.3 [00540]embedded image (500 MHz, Chloroform-d) δ 7.61 (d, J = 2.5 Hz, 1H), 7.46 (d, J = 2.5 Hz, 1H), 7.18 (s, 1H), 5.85 (s, 1H). 465 CF.sub.3 [00541]embedded image (500 MHz, Chloroform-d) δ 7.42 (d, J = 2.5 Hz, 1H), 7.36 (s, 1H), 7.20 (d, J = 2.5 Hz, 1H), 7.19 (s, 1H), 5.74 (s, 1H). 466 CF.sub.3 [00542]embedded image (500 MHz, Chloroform-d) δ 7.33 (d, J = 2.5 Hz, 1H), 7.16 (s, 1H), 7.08 (d, J = 2.5 Hz, 1H), 6.00 (s, 1H), 2.86 (q, J = 8.0 Hz, 2H), 1.32 (t, J = 8.0 Hz, 3H). 467 CF.sub.3 [00543]embedded image (500 MHz, Chloroform-d) δ 7.56 (s, 1H), 7.18 (s, 1H), 6.92 (s, 1H), 5.74 (s, 1H), 2.61 (t, J = 7.5 Hz, 2H), 1.51-1.37 (m, 4H), 0.96 (t, J = 7.5 Hz, 3H). 468 CF.sub.3 [00544]embedded image (500 MHz, Chloroform-d) δ 7.41 (s, 1H), 7.13 (s, 1H), 7.03 (s, 1H), 5.74 (s, 1H), 2.65 (t, J = 7.5 Hz, 2H), 1.74- 1.61 (m, 2H), 0.99 (t, J = 8.0 Hz, 3H). 469 CF.sub.3 [00545]embedded image (500 MHz, Chloroform-d) δ 7.93 (d, J = 2.5 Hz, 1H), 7.33 (d, J = 2.5 Hz, 1H), 7.11 (s, 1H), 5.65 (s, 1H). 470 CF.sub.3 [00546]embedded image (500 MHz, Chloroform-d) δ 7.18 (s, 1H), 6.32 (s, 1H), 6.27 (s, 1H), 5.95 (s, 1H), 5.84 (s, 1H). 471 CF.sub.3 [00547]embedded image (500 MHz, Chloroform-d) δ 7.85 (s, 1H), 7.56 (s, 1H), 7.17 (s, 1H), 5.69 (s, 1H). 472 CF.sub.3 [00548]embedded image (500 MHz, Chloroform-d) δ 7.68 (d, J = 2.5 Hz, 1H), 7.31 (d, J = 2.5 Hz, 1H), 7.15 (s, 1H), 5.75 (s, 1H), 4.31 (q, J = 7.0 Hz, 2H), 1.33 (t, J = 7.0 Hz, 3H). 473 CF.sub.3 [00549]embedded image (500 MHz, Chloroform-d) δ 9.16 (s, 1H), 8.50 (s, 1H), 7.13 (s, 1H), 5.86 (s, 1H), 3.45 (q, J = 6.5 Hz, 2H), 1.43 (t, J = 6.5 Hz, 3H). 474 CF.sub.3 [00550]embedded image (500 MHz, Chloroform-d) δ 9.87 (s, 1H), 8.30 (s, 1H), 7.84 (s, 1H), 7.14 (s, 1H), 5.93 (s, 1H). 475 CF.sub.3 [00551]embedded image (500 MHz, Chloroform-d) δ 7.80 (d, J = 2.5 Hz, 1H), 7.73 (d, J = 2.5 Hz, 1H), 7.17 (s, 1H), 5.90 (s, 1H), 2.51 (s, 3H). 476 CF.sub.3 [00552]embedded image (500 MHz, Chloroform-d) δ 7.69 (s, 1H), 7.17 (s, 1H), 6.30-6.23 (m, 1H), 6.19 (s, 1H), 6.10-6.01 (m, 1H), 1.70 (d, J = 6.5 Hz, 3H). 477 CF.sub.3 [00553]embedded image (500 MHz, Chloroform-d) δ 7.50 (s, 1H), 7.20 (s, 1H), 7.07 (s, 1H). 478 CF.sub.3 [00554]embedded image (500 MHz, Chloroform-d) δ 7.20 (s, 1H), 6.63 (d, J = 7.5 Hz, 1H), 6.00 (s, 1H), 2.23 (s, 3H). 479 CF.sub.3 [00555]embedded image (500 MHz, Chloroform-d) δ 7.92 (s, 1H), 7.20 (s, 1H), 6.64 (s, 1H), 2.40 (s, 3H). 480 CF.sub.3 [00556]embedded image (500 MHz, Chloroform-d) δ 7.19 (s, 1H), 6.70 (s, 1H), 2.46 (s, 3H), 2.36 (s, 3H), 2.30 (s, 3H). 481 CF.sub.3 [00557]embedded image (500 MHz, Chloroform-d) δ 7.20 (s, 1H), 6.00 (s, 1H), 2.44 (s, 3H), 2.24 (s, 3H). 482 CF.sub.3 [00558]embedded image (500 MHz, Chloroform-d) δ 8.22 (d, J = 2.5 Hz, 1H), 7.71 (d, J = 2.5 Hz, 1H), 7.21 (s, 1H), 7.15 (s, 1H). 483 CF.sub.3 [00559]embedded image (500 MHz, Chloroform-d) δ 7.20 (s, 1H), 7.10 (s, 1H), 6.86 (s, 1H), 6.05 (s, 1H), 3.26 (q, J = 8.0 Hz, 2H), 2.98 (s, 3H), 1.19 (t, J = 8.0 Hz, 3H). 484 CF.sub.3 [00560]embedded image (500 MHz, Chloroform-d) δ 8.60 (s, 1H), 7.85 (d, J = 2.5 Hz, 1H), 7.76 (d, J = 2.5 Hz, 1H), 7.37 (s, 1H), 3.15 (s, 3H). 485 CF.sub.3 [00561]embedded image (500 MHz, Chloroform-d) δ 7.50 (s, 1H), 7.20 (s, 1H), 7.15 (s, 1H), 2.52 (s, 3H). 486 CF.sub.3 [00562]embedded image (500 MHz, Chloroform-d) δ 7.25 (s, 1H), 7.22-7.16 (m, 2H), 6.55 (s, 1H), 4.46 (q, J = 9.5 Hz, 2H). 487 CF.sub.3 [00563]embedded image (500 MHz, Chloroform-d) δ 7.25 (s, 1H), 7.22 (s, 1H), 6.55 (s, 1H), 2.31 (s, 3H), 2.21 (s, 3H). 488 CF.sub.3 [00564]embedded image (500 MHz, Chloroform-d) δ 7.13 (s, 1H), 6.19 (s, 1H), 5.72 (s, 1H), 3.52 (s, 1H). 489 CF.sub.3 [00565]embedded image (500 MHz, Chloroform-d) δ 7.13 (s, 1H), 6.84 (s, 1H), 5.65 (s, 1H), 2.71 (q, J = 8.0 Hz, 2H), 2.41 (s, 3H), 1.26 (t, J = 8.0 Hz, 3H). 490 CF.sub.3 [00566]embedded image (500 MHz, Chloroform-d) δ 7.13 (s, 1H), 5.68 (s, 1H), 3.52 (s, 1H), 2.40 (s, 3H), 2.30 (s, 3H), 2.26 (s, 3H). 491 CF.sub.3 [00567]embedded image (500 MHz, Chloroform-d) δ 7.13 (s, 1H), 5.68 (s, 1H), 2.40 (d, J = 7.1 Hz, 6H), 2.26 (s, 3H). 492 CF.sub.3 [00568]embedded image (500 MHz, Chloroform-d) δ 8.03 (s, 1H), 7.21 (s, 1H), 7.13 (s, 1H), 6.00 (s, 1H), 1.50-1.41 (m, 1H), 0.91-0.79 (m, 4H). 493 CF.sub.3 [00569]embedded image (500 MHz, Chloroform-d) δ 7.33 (s, 1H), 7.24 (s, 1H), 7.14 (s, 1H), 6.00 (s, 1H), 2.32-2.22 (m, 1H), 2.04-1.91 (m, 4H), 1.78-1.62 (m, 6H). 494 CF.sub.3 [00570]embedded image (500 MHz, Chloroform-d) δ 7.38 (d, J = 2.5 Hz, 1H), 7.18 (s, 1H), 5.47 (d, J = 2.5 Hz, 1H), 5.30 (s, 1H), 2.21 (s, 3H). 495 CF.sub.3 [00571]embedded image (500 MHz, Chloroform-d) δ 7.16 (s, 1H), 6.88 (s, 1H), 5.97 (s, 1H), 3.31 (hept, J = 6.5 Hz, 1H), 2.37 (s, 3H), 1.30 (d, J = 6.5 Hz, 6H). 496 CF.sub.3 [00572]embedded image (500 MHz, Chloroform-d) δ 7.18 (s, 1H), 7.06 (s, 1H), 5.88 (s, 1H), 3.50 (s, 2H), 2.46 (s, 3H). 497 CF.sub.3 [00573]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ11.71 (s, 1H), 8.13 (s, 1H), 7.76 (s, 1H), 6.88 (s, 1H). 498 CF.sub.3 [00574]embedded image (500 MHz, Chloroform-d) δ 8.35 (s, 1H), 7.20 (s, 1H), 6.98 (s, 1H), 2.77 (s, 3H). 499 CF.sub.3 [00575]embedded image (500 MHz, Chloroform-d) δ 7.98 (s, 1H), 7.35 (s, 1H), 7.20 (s, 1H). 500 CF.sub.3 [00576]embedded image (500 MHz, Chloroform-d) δ 9.43 (s, 1H), 7.20 (s, 1H), 6.82 (s, 1H), 4.00 (s, 3H). 501 CF.sub.3 [00577]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 10.60 (s, 1H), 8.11 (d, J = 2.5 Hz, 1H), 7.37 (d, J = 2.5 Hz, 1H), 6.89 (s, 1H). 502 CF.sub.3 [00578]embedded image (500 MHz, Chloroform-d) δ 7.12 (s, 1H), 5.79 (s, 1H), 2.46 (s, 3H). 503 CF.sub.3 [00579]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ11.73 (s, 1H), 9.42 (s, 1H), 6.84 (s, 1H). 504 CF.sub.3 [00580]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 12.25 (s, 1H), 9.12 (s, 1H), 6.89 (s, 1H), 3.79 (s, 3H). 505 CF.sub.3 [00581]embedded image (500 MHz, Chloroform-d) δ 7.12 (s, 1H), 5.71 (s, 1H). 506 CF.sub.3 [00582]embedded image (500 MHz, Chloroform-d) δ 9.35 (s, 1H), 7.10 (s, 1H). 507 CF.sub.3 [00583]embedded image (500 MHz, Chloroform-d) δ 8.11 (s, 1H), 7.18 (s, 1H). 508 CF.sub.3 [00584]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.34 (s, 1H), 8.23 (s, 1H), 6.82 (s, 1H). 509 CF.sub.3 [00585]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.19 (s, 1H), 8.30 (s, 1H), 6.79 (s, 1H). 510 CF.sub.3 [00586]embedded image (500 MHz, Chloroform-d) δ 8.44 (s, 1H), 7.17 (s, 1H). 511 CF.sub.3 [00587]embedded image (500 MHz, Chloroform-d) δ 7.15 (s, 1H), 5.75 (s, 1H), 2.54 (s, 3H), 2.49 (s, 3H). 512 CF.sub.3 [00588]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 12.67 (s, 1H), 9.20 (s, 1H), 8.10 (s, 1H), 6.88 (s, 1H). 513 CF.sub.3 [00589]embedded image (500 MHz, Chloroform-d) δ 7.85 (s, 1H), 7.30 (s, 1H), 7.18 (s, 1H). 514 CF.sub.3 [00590]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.38 1H), 8.18 (s, 1H), 8.10 (s, 1H), 7.12, 1H). 515 CF.sub.3 [00591]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.01 (s, 1H), 8.72 (s, 1H), 7.89 (s, 1H), 6.94 (s, 1H). 516 CF.sub.3 [00592]embedded image (500 MHz, Chloroform-d) δ 9.14 (s, 1H), 7.08 (s, 1H). 517 CF.sub.3 [00593]embedded image (500 MHz, Chloroform-d) δ 9.32 (s, 1H), 7.11 (s, 1H), 5.77 (s, 1H). 518 CF.sub.3 [00594]embedded image (500 MHz, Chloroform-d) δ 7.19 (s, 1H), 2.54 (s, 3H). 519 CF.sub.3 [00595]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 12.59 (s, 1H), 8.19 (s, 1H), 6.84 (s, 1H). 520 CF.sub.3 [00596]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 12.73 (s, 1H), 9.49 (s, 1H), 6.82 (s, 1H). 521 CF.sub.3 [00597]embedded image (500 MHz, Chloroform-d) δ 7.16 (s, 1H), 2.68 (s, 3H). 522 CF.sub.3 [00598]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 12.88 (s, 1H), 7.92 (d, J = 2.5 Hz, 1H), 7.37 (d, J = 2.5 Hz, 1H), 6.87 (s, 1H). 523 CF.sub.3 [00599]embedded image (500 MHz, Chloroform-d) δ 7.20 (s, 1H), 6.89 (d, J = 7.5 Hz, 1H), 6.00 (s, 1H). 524 CF.sub.3 [00600]embedded image (500 MHz, Chloroform-d) δ 7.31 (s, 1H), 7.19 (s, 1H). 525 CF.sub.3 [00601]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 12.11 (s, 1H), 8.74 (d, J = 2.5 Hz, 1H), 7.26 (d, J = 2.5 Hz, 1H), 6.88 (s, 1H). 526 CF.sub.3 [00602]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 12.47 (s, 1H), 8.72 (d, J = 2.0 Hz, 1H), 7.40 (d, J = 2.0 Hz, 1H), 6.85 (s, 1H). 527 CF.sub.3 [00603]embedded image (500 MHz, Chloroform-d) δ 9.48 (s, 2H), 7.07 (s, 1H), 5.93 (s, 1H). 528 CF.sub.3 [00604]embedded image (500 MHz, Chloroform-d) δ 8.58 (s, 1H), 8.37 (s, 1H), 7.10 (s, 1H), 5.93 (s, 1H). 529 CF.sub.3 [00605]embedded image (500 MHz, Chloroform-d) δ 7.75 (d, J = 2.5 Hz, 1H), 7.15 (s, 1H), 6.76 (d, J = 2.5 Hz, 1H), 5.95 (s, 1H). 530 CF.sub.3 [00606]embedded image .sup.1H NMR (500 MHz, DMSO-d6) δ 13.41 (s, 1H), 8.81 (d, J = 2.5 Hz, 1H), 8.04 (s, 1H), 7.69 (d, J = 2.5 Hz, 1H), 6.74 (s, 1H). 531 CF.sub.3 [00607]embedded image (500 MHz, Chloroform-d) δ 7.29 (s, 2H), 7.22 (s, 1H). 532 CF.sub.3 [00608]embedded image (500 MHz, Chloroform-d) δ 7.33 (d, J = 2.5 Hz, 1H), 7.18 (s, 1H), 6.77 (d, J = 2.5 Hz, 1H). 533 CF.sub.3 [00609]embedded image (500 MHz, Chloroform-d) δ 7.88 (d, J = 2.5 Hz, 1H), 7.53 (d, J = 2.0 Hz, 1H), 7.26 (s, 1H), 6.62 (dd, J = 2.5, 2.0 Hz, 1H), 5.93 (s, 1H). 534 CF.sub.3 [00610]embedded image (500 MHz, Chloroform-d) δ 7.15 (s, 1H), 2.34 (s, 3H), 2.28 (s, 3H). 535 CF.sub.3 [00611]embedded image (500 MHz, Chloroform-d) δ 7.55 (s, 1H), 7.17 (s, 1H), 4.01 (s, 3H). 536 CF.sub.3 [00612]embedded image (500 MHz, Chloroform-d) δ 7.19 (s, 1H), 7.15 (s, 1H), 2.17 (s, 3H). 537 CF.sub.3 [00613]embedded image (500 MHz, Chloroform-d) δ 7.44 (s, 1H), 7.36 (s, 1H), 7.27 (s, 1H), 5.93 (s, 1H). 538 CF.sub.3 [00614]embedded image (500 MHz, Chloroform-d) δ 7.48 (s, 1H), 7.15 (s, 1H), 2.66 (q, J = 8.0 Hz, 2H), 1.30 (t, J = 8.0 Hz, 3H). 539 CF.sub.3 [00615]embedded image (500 MHz, Chloroform-d) δ 7.47 (s, 1H), 7.15 (s, 1H), 2.60 (s, 3H). 540 CF.sub.3 [00616]embedded image (500 MHz, Chloroform-d) δ 7.18 (s, 1H), 6.42 (s, 1H), 3.86 (s, 3H), 2.35 (s, 3H). 541 CF.sub.3 [00617]embedded image (500 MHz, Chloroform-d) δ 7.51 (d, J = 2.5 Hz, 1H), 7.26 (s, 1H), 6.13 (d, J = 2.5 Hz, 1H), 5.93 (s, 1H), 2.38 (s, 3H). 542 CF.sub.3 [00618]embedded image (500 MHz, Chloroform-d) δ 7.16 (s, 1H), 7.05 (s, 1H). 543 CF.sub.3 [00619]embedded image (500 MHz, Chloroform-d) δ 7.21 (s, 1H), 2.56 (s, 6H). 544 CF.sub.3 [00620]embedded image (500 MHz, Chloroform-d) δ 7.18 (s, 1H), 2.22 (s, 3H), 2.12 (s, 3H). 545 CF.sub.3 [00621]embedded image (500 MHz, Chloroform-d) δ 7.26 (s, 1H), 6.07 (s, 1H), 5.93 (s, 1H), 2.40 (s, 3H), 1.75 (s, 3H). 546 CF.sub.3 [00622]embedded image .sup.1H NMR (500 MHz, DMSO-d6) δ 13.03 (s, 1H), 8.55 (s, 1H), 8.23 (s, 1H), 7.47 (s, 1H), 4.17 (t, J = 6.5 Hz, 2H), 1.83- 1.66 (m, 2H), 0.85 (t, J = 7.5 Hz, 3H). 547 CF.sub.3 [00623]embedded image (500 MHz, Chloroform-d) δ 7.15 (s, 1H), 7.01-6.81 (m, 2H), 6.37-6.23 (m, 1H), 5.92 (s, 1H). 548 CF.sub.3 [00624]embedded image (500 MHz, Chloroform-d) δ 8.18 (s, 1H), 7.15 (s, 1H), 7.07 (s, 1H), 6.88 (d, J = 2.5 Hz, 1H), 6.33 (d, J = 2.5 Hz, 1H), 5.81 (s, 1H). 549 CF.sub.3 [00625]embedded image (500 MHz, Chloroform-d) δ 7.33-7.21 (m, 2H), 7.13 (s, 1H), 6.33-6.21 (m, 2H), 5.93 (s, 1H). 550 CF.sub.3 [00626]embedded image (500 MHz, Chloroform-d) δ 8.80 (s, 1H), 7.19 (s, 1H), 7.05 (d, J = 2.5 Hz, 1H), 6.55 (d, J = 2.5 Hz, 1H), 5.39 (s, 1H). 551 CF.sub.3 [00627]embedded image (500 MHz, Chloroform-d) δ 8.07 (s, 1H), 7.20 (s, 1H), 6.74 (s, 1H), 6.66 (s, 1H), 6.00 (s, 1H), 2.15 (s, 3H). 552 CF.sub.3 [00628]embedded image (500 MHz, Chloroform-d) δ 7.37 (d, J = 2.5 Hz, 1H), 7.13 (s, 1H), 6.43 (s, 1H), 5.93 (s, 1H), 5.82 (d, J = 2.5 Hz, 1H), 3.85 (s, 3H). 553 CF.sub.3 [00629]embedded image (500 MHz, Chloroform-d) δ 7.19 (s, 1H), 6.45 (s, 1H), 6.32-6.26 (m, 2H), 3.71 (s, 3H), 2.63 (q, J = 8.0 Hz, 2H), 1.25 (t, J = 8.0 Hz, 3H). 554 CF.sub.3 [00630]embedded image (500 MHz, Chloroform-d) δ 7.92 (s, 1H), 7.21 (s, 1H), 6.58 (s, 1H), 5.94 (s, 1H), 5.86 (s, 1H), 2.30 (s, 3H). 555 CF.sub.3 [00631]embedded image (500 MHz, Chloroform-d) δ 7.24 (s, 1H), 6.94 (d, J = 2.5 Hz, 1H), 6.24 (dd, J = 2.5, 2.0 Hz, 1H), 6.09 (d, J = 2.0 Hz, 1H), 5.93 (s, 1H), 2.21 (s, 3H). 556 CF.sub.3 [00632]embedded image (500 MHz, Chloroform-d) δ 8.50 (s, 1H), 7.22 (s, 1H), 6.54 (d, J = 2.5 Hz, 1H), 6.00 (d, J = 2.5 Hz, 1H), 5.74 (s, 1H), 2.33 (s, 3H). 557 CF.sub.3 [00633]embedded image (500 MHz, Chloroform-d) δ 7.87 (s, 1H), 7.19 (s, 1H), 6.67 (d, J = 2.5 Hz, 1H), 6.18 (s, 1H), 6.05 (d, J = 2.5 Hz, 1H), 2.42 (s, 3H). 558 CF.sub.3 [00634]embedded image 559 CF.sub.3 [00635]embedded image (500 MHz, Chloroform-d) δ 9.53 (s, 1H), 8.99-8.88 (m, 2H), 7.29 (s, 1H). 560 CF.sub.3 [00636]embedded image (500 MHz, Chloroform-d) δ 9.61 (s, 1H), 9.55 (s, 1H), 9.41 (s, 1H), 7.28 (s, 1H), 5.74 (s, 1H). 561 CF.sub.3 [00637]embedded image (500 MHz, Chloroform-d) δ 9.55 (s, 1H), 8.63 (s, 1H), 7.36 (s, 1H). 562 CF.sub.3 [00638]embedded image (500 MHz, Chloroform-d) δ 9.39 (d, J = 1.5 Hz, 1H), 9.23 (d, J = 1.5 Hz, 1H), 8.57 (s, 1H), 7.28 (s, 1H), 5.94 (s, 1H). 563 CF.sub.3 [00639]embedded image (500 MHz, Chloroform-d) δ 9.99 (s, 1H), 8.78 (s, 1H), 7.87 (s, 1H), 7.29 (s, 1H), 5.54 (s, 1H). 564 CF.sub.3 [00640]embedded image (500 MHz, Chloroform-d) δ 9.23 (d, J = 1.5 Hz, 1H), 7.84 (d, J = 1.5 Hz, 1H), 7.53 (d, J = 2.5 Hz, 1H), 7.28 (s, 1H), 7.22 (d, J = 2.5 Hz, 1H), 5.92 (s, 1H). 565 CF.sub.3 [00641]embedded image (500 MHz, Chloroform-d) δ 9.61 (s, 1H), 9.55 (s, 1H), 9.42 (s, 1H), 7.28 (s, 1H), 5.74 (s, 1H). 566 CF.sub.3 [00642]embedded image (500 MHz, Chloroform-d) δ 9.53 (s, 1H), 8.99-8.88 (m, 2H), 7.29 (s, 1H), 5.34 (s, 1H). 567 CF.sub.3 [00643]embedded image (500 MHz, Chloroform-d) δ 9.35 (s, 1H), 8.25 (s, 1H), 7.25 (s, 1H). 568 CF.sub.3 [00644]embedded image (500 MHz, Chloroform-d) δ 8.75 (q, J = 1.5 Hz, 1H), 8.35 (q, J = 1.5 Hz, 1H), 7.28 (s, 1H), 2.39 (s, 3H). 569 CF.sub.3 [00645]embedded image (500 MHz, Chloroform-d) δ 9.84 (s, 1H), 8.75 (d, J = 5.5 Hz, 1H), 7.56 (d, J = 5.5 Hz, 1H), 7.28 (s, 1H). 570 CF.sub.3 [00646]embedded image (500 MHz, Chloroform-d) δ 8.91 (dd, J = 5.5, 1.5 Hz, 1H), 7.70 (dd, J = 7.5, 5.5 Hz, 1H), 7.49 (dd, J = 7.5, 1.5 Hz, 1H), 7.43 (s, 1H), 7.28 (s, 1H). 571 CF.sub.3 [00647]embedded image (500 MHz, Chloroform-d) δ 8.45-8.36 (m, 3H), 8.24-8.01 (m, 3H), 7.89- 7.79 (m, 1H), 7.54-7.45 (m, 2H), 7.10 (s, 1H), 5.56 (s, 1H). 572 CF.sub.3 [00648]embedded image (500 MHz, Chloroform-d) δ 8.95-8.91 (m, 1H), 8.59-8.55 (m, 1H), 8.37- 8.30 (m, 1H), 8.22-8.12 (m, 2H), 7.92- 7.74 (m, 3H), 7.11 (s, 1H), 5.55 (s, 1H). 573 CF.sub.3 [00649]embedded image (500 MHz, Chloroform-d) δ 8.86-8.31 (m, 3H), 8.04-7.90 (m, 3H), 7.75- 7.68 (m, 2H), 7.63-7.55 (m, 1H), 7.10 (s, 1H), 5.52 (s, 1H). 574 CF.sub.3 [00650]embedded image (500 MHz, Chloroform-d) δ 9.08-8.84 (m, 1H), 8.12-7.91 (m, 4H), 7.74- 7.58 (m, 4H), 7.10 (s, 1H), 5.66 (s, 1H). 575 CF.sub.3 [00651]embedded image (500 MHz, Chloroform-d) δ 8.90-8.84 (m, 2H), 8.58-8.37 (m, 2H), 7.91- 7.80 (m, 2H), 7.68-7.63 (m, 2H), 7.10 (s, 1H), 5.61 (s, 1H). 576 CF.sub.3 [00652]embedded image (500 MHz, Chloroform-d) δ 8.51 (d, J = 2.0 Hz, 1H), 8.32-8.26 (m, 3H), 7.89- 7.80 (m, 3H), 7.03 (s, 1H), 5.87 (s, 1H). 577 CF.sub.3 [00653]embedded image (500 MHz, Chloroform-d) δ 8.43 (d, J = 2.0 Hz, 1H), 8.26-8.06 (m, 2H), 7.95- 7.90 (m, 1H), 7.45-7.39 (m, 2H), 7.08 (s, 1H), 5.71 (s, 1H), 2.30 (s, 3H). 578 CF.sub.3 [00654]embedded image (500 MHz, Chloroform-d) δ 8.55-8.45 (m, 2H), 8.27-8.20 (m, 2H), 8.11- 7.97 (m, 2H), 7.72-7.54 (m, 2H), 7.10 (s, 1H), 5.50 (s, 1H). 579 CF.sub.3 [00655]embedded image (500 MHz, Chloroform-d) δ 8.61 (d, J = 1.5 Hz, 1H), 8.39 (d, J = 7.5 Hz, 1H), 8.14-8.10 (m, 3H), 7.80-7.67 (m, 2H), 7.05 (s, 1H), 5.75 (s, 1H). 580 CF.sub.3 [00656]embedded image (500 MHz, Chloroform-d) δ 9.42-9.13 (m, 2H), 8.59-8.49 (m, 2H), 7.97- 7.88 (m, 2H), 7.68-7.56 (m, 1H), 7.28 (s, 1H), 5.76 (s, 1H). 581 CF.sub.3 [00657]embedded image (500 MHz, Chloroform-d) δ 9.08 (s, 1H), 7.50-7.23 (m, 2H), 7.16-7.11 (m, 2H), 7.05-6.91 (m, 2H), 6.89- 6.77 (m, 2H), 5.48 (s, 1H). 582 CF.sub.3 [00658]embedded image (500 MHz, Chloroform-d) δ 8.28-8.12 (m, 2H), 7.83 (d, J = 1.5 Hz, 1H), 7.59- 7.51 (m, 2H), 7.55 (s, 1H), 7.34-7.26 (m, 2H), 7.09 (s, 1H), 5.72 (s, 1H). 583 CF.sub.3 [00659]embedded image (500 MHz, Chloroform-d) δ 8.33-8.27 (m, 2H), 7.70-7.62 (m, 2H), 7.60- 7.53 (m, 2H), 7.34-7.26 (m, 2H), 7.03 (s, 1H), 5.84 (s, 1H). 584 CF.sub.3 [00660]embedded image (500 MHz, Chloroform-d) δ 8.05-7.95 (m, 2H), 7.86-7.65 (m, 2H), 7.54- 7.44 (m, 2H), 7.35-7.23 (m, 1H), 7.09 (s, 1H), 5.76 (s, 1H). 585 CF.sub.3 [00661]embedded image (500 MHz, Chloroform-d) δ 8.14 (d, J = 1.5 Hz, 1H), 8.05 (dd, J = 7.5, 1.5 Hz, 1H), 7.79-7.73 (m, 2H), 7.54-7.44 (m, 2H), 7.35-7.28 (m, 1H), 7.04 (s, 1H), 5.89 (s, 1H). 586 CF.sub.3 [00662]embedded image (500 MHz, Chloroform-d) δ 8.52 (dd, J = 7.5, 1.5 Hz, 1H), 8.42 (dd, J = 7.0, 1.5 Hz, 1H), 7.96-7.81 (m, 2H), 7.60- 7.51 (m, 2H), 7.31-7.20 (m, 1H), 7.06 (s, 1H), 5.76 (s, 1H). 587 CF.sub.3 [00663]embedded image (500 MHz, Chloroform-d) δ 8.23 (s, 1H), 7.96-7.51 (m, 3H), 7.18 (d, J = 2.5 Hz, 1H), 7.08 (s, 1H), 6.68-6.51 (m, 1H), 5.75 (s, 1H). 588 CF.sub.3 [00664]embedded image (500 MHz, Chloroform-d) δ 8.06 (s, 1H), 7.90-7.80 (m, 2H), 7.58 (dd, J = 7.5, 1.5 Hz, 1H), 7.18 (d, J = 7.5 Hz, 1H), 7.02 (s, 1H), 6.56-6.47 (m, 1H), 5.82 (s, 1H). 589 CF.sub.3 [00665]embedded image (500 MHz, Chloroform-d) δ 8.06 (s, 1H), 7.90-7.80 (m, 2H), 7.58 (dd, J = 7.5, 1.5 Hz, 1H), 7.18 (d, J = 7.5 Hz, 1H), 7.02 (s, 1H), 6.56-6.45 (m, 1H), 5.82 (s, 1H). 590 CF.sub.3 [00666]embedded image (500 MHz, Chloroform-d) δ 7.77 (d, J = 1.5 Hz, 1H), 7.65 (d, J = 1.0 Hz, 1H), 7.14-7.05 (m, 3H), 6.62 (dd, J = 7.5, 1.5 Hz, 1H), 5.72 (s, 1H), 3.74 (s, 3H). 591 CF.sub.3 [00667]embedded image 592 CF.sub.3 [00668]embedded image (500 MHz, Chloroform-d) δ 8.02-7.93 (m, 2H), 7.65 (dd, J = 7.5, 1.5 Hz, 1H), 7.09 (s, 1H). 593 CF.sub.3 [00669]embedded image (500 MHz, Chloroform-d) δ 8.11-8.03 (m, 2H), 7.67 (dd, J = 7.5, 1.5 Hz, 1H), 7.17 (s, 1H), 7.09 (s, 1H), 5.68 (s, 1H), 2.50 (s, 3H). 594 CF.sub.3 [00670]embedded image .sup.1H NMR (500 MHz, DMSO-d6) δ 13.86 (s, 1H), 8.57 (s, 1H), 7.99-7.81 (m, 2H), 7.48-7.36 (m, 2H), 7.29 (s, 1H). 595 CF.sub.3 [00671]embedded image (500 MHz, Chloroform-d) δ 7.83 (d, J = 1.5 Hz, 1H), 7.66-7.58 (m, 3H), 7.08 (s, 1H), 6.76 (dd, J = 7.5, 1.5 Hz, 1H), 5.63 (s, 1H). 596 CF.sub.3 [00672]embedded image (500 MHz, Chloroform-d) δ 9.33 (s, 1H), 8.31 (d, J = 1.5 Hz, 1H), 8.16 (d, J = 7.5 Hz, 1H), 7.81 (dd, J = 7.5, 1.5 Hz, 1H), 7.08 (s, 1H), 5.81 (s, 1H). 597 CF.sub.3 [00673]embedded image (500 MHz, Chloroform-d) δ 7.85 (d, J = 1.5 Hz, 1H), 7.79 (d, J = 7.5 Hz, 1H), 7.67 (dd, J = 7.5, 1.5 Hz, 1H), 7.03 (s, 1H), 5.84 (s, 1H), 2.61 (s, 3H). 598 CF.sub.3 [00674]embedded image (500 MHz, Chloroform-d) δ 8.25 (s, 1H), 7.99 (d, J = 1.5 Hz, 1H), 7.71 (d, J = 7.5 Hz, 1H), 7.59 (dd, J = 7.5, 1.5 Hz, 1H), 7.07 (s, 1H), 5.84 (s, 1H). 599 CF.sub.3 [00675]embedded image (500 MHz, Chloroform-d) δ 7.66 (d, J = 1.5 Hz, 1H), 7.58 (d, J = 7.5 Hz, 1H), 7.46 (dd, J = 7.5, 1.5 Hz, 1H), 7.06 (s, 6.75-6.69 (m, 1H), 6.45-6.33 (m, 1H), 5.60 (s, 1H), 3.22-3.12 (m, 2H). 600 CF.sub.3 [00676]embedded image (500 MHz, Chloroform-d) δ 9.18 (s, 1H), 8.09-8.00 (m, 1H), 7.31-7.25 (m, 2H), 7.21-7.15 (m, 2H), 5.98 (s, 1H). 601 CF.sub.3 [00677]embedded image 602 CF.sub.3 [00678]embedded image (500 MHz, Chloroform-d) δ 8.36 (d, J = 1.5 Hz, 1H), 8.06 (d, J = 7.5 Hz, 1H), 7.73 (dd, J = 7.5, 1.5 Hz, 1H), 7.15 (s, 1H), 5.93 (s, 1H). 603 CF.sub.3 [00679]embedded image (500 MHz, Chloroform-d) δ 8.22 (d, J = 1.5 Hz, 1H), 8.05 (d, J = 7.5 Hz, 1H), 7.66 (dd, J = 7.5, 1.5 Hz, 1H), 7.42 (d, J = 2.5 Hz, 1H), 7.32 (dd, J = 2.5, 1.6 Hz, 1H), 7.08 (s, 1H), 5.67 (s, 1H). 604 CF.sub.3 [00680]embedded image (500 MHz, Chloroform-d) δ 7.76 (d, J = 1.5 Hz, 1H), 7.69 (d, J = 7.5 Hz, 1H), 7.58 (dd, J = 7.5, 1.5 Hz, 1H), 7.08 (s, 1H), 6.28 (s, 1H), 5.71 (s, 1H), 2.86 (q, J = 8.0 Hz, 2H), 1.32 (t, J = 8.0 Hz, 3H). 605 CF.sub.3 [00681]embedded image (500 MHz, Chloroform-d) δ 9.34 (s, 1H), 8.38 (d, J = 1.5 Hz, 1H), 7.86 (d, J = 7.5 Hz, 1H), 7.78 (dd, J = 7.5, 1.5 Hz, 1H), 7.08 (s, 1H), 5.64 (s, 1H). 606 CF.sub.3 [00682]embedded image (500 MHz, Chloroform-d) δ 8.30 (s, 1H), 7.79-7.70 (m, 2H), 7.49 (dd, J = 7.5, 1.5 Hz, 1H), 7.02 (s, 1H), 5.82 (s, 1H). 607 CF.sub.3 [00683]embedded image (500 MHz, Chloroform-d) δ 8.41 (s, 1H), 7.95 (d, J = 1.5 Hz, 1H), 7.79 (d, J = 7.5 Hz, 1H), 7.60 (dd, J = 7.5, 1.5 Hz, 1H), 7.08 (s, 1H), 5.64 (s, 1H), 4.55 (q, J = 8.0 Hz, 2H), 1.63 (t, J = 8.0 Hz, 3H). 608 CF.sub.3 [00684]embedded image (500 MHz, Chloroform-d) δ 7.23 (d, J = 7.5 Hz, 1H), 7.15-7.07 (m, 2H), 6.59 (dd, J = 7.5, 1.5 Hz, 1H), 6.49 (d, J = 1.5 Hz, 1H), 5.87 (s, 1H), 3.10 (s, 2H), 2.90 (s, 6H). 609 CF.sub.3 [00685]embedded image (500 MHz, Chloroform-d) δ 7.82-7.74 (m, 2H), 7.73 (d, J = 1.5 Hz, 1H), 7.11 (d, J = 2.5 Hz, 1H), 7.02 (s, 1H), 6.50 (d, J = 2.5 Hz, 1H), 5.82 (s, 1H), 3.80 (s, 3H). 610 CF.sub.3 [00686]embedded image 611 CF.sub.3 [00687]embedded image (500 MHz, Chloroform-d) δ 8.30 (d, J = 1.5 Hz, 1H), 7.82-7.72 (m, 2H), 7.02 (s, 1H), 5.79 (s, 1H), 4.30 (s, 3H). 612 CF.sub.3 [00688]embedded image (500 MHz, Chloroform-d) δ 7.80-7.71 (m, 2H), 7.33-7.25 (m, 2H), 6.17 (s, 1H), 2.49 (s, 3H). 613 CF.sub.3 [00689]embedded image (500 MHz, Chloroform-d) δ 7.66-7.55 (m, 2H), 7.32-7.24 (m, 2H), 7.26- 7.18 (m, 2H), 6.04 (s, 1H). 614 CF.sub.3 [00690]embedded image (500 MHz, Chloroform-d) δ 8.18-8.08 (m, 2H), 7.58-7.50 (m, 2H), 7.29 (s, 1H). 615 CF.sub.3 [00691]embedded image (500 MHz, Chloroform-d) δ 7.72-7.58 (m, 3H), 7.29 (s, 1H). 616 CF.sub.3 [00692]embedded image (500 MHz, Chloroform-d) δ 7.66-7.52 (m, 2H), 7.30-7.20 (m, 2H), 7.09 (s, 1H). 617 CF.sub.3 [00693]embedded image 618 CF.sub.3 [00694]embedded image (500 MHz, Chloroform-d) δ 7.86 (s, 1H), 7.16 (d, J = 2.0 Hz, 1H), 7.08 (dd, J = 7.5, 2.0 Hz, 1H), 6.99 (d, J = 7.5 Hz, 1H), 5.34 (s, 1H), 4.32-4.25 (m, 4H). 619 CF.sub.3 [00695]embedded image 620 CF.sub.3 [00696]embedded image 621 CF.sub.3 [00697]embedded image 622 CF.sub.3 [00698]embedded image (500 MHz, Chloroform-d) δ 9.72 (d, J = 1.5 Hz, 1H), 9.43 (d, J = 7.5 Hz, 1H), 8.03 (dd, J = 7.5, 1.5 Hz, 1H), 7.24 (s, 1H), 5.86 (s, 1H). 623 CF.sub.3 [00699]embedded image (500 MHz, Chloroform-d) δ 9.50 (dd, J = 7.5, 1.5 Hz, 1H), 8.01 (dd, J = 7.0, 1.5 Hz, 1H), 7.82 (dd, J = 7.5, 7.0 Hz, 1H), 7.23 (s, 1H), 5.77 (s, 1H). 624 CF.sub.3 [00700]embedded image (500 MHz, Chloroform-d) δ 9.50 (s, 1H), 9.42 (s, 1H), 7.28 (s, 1H), 5.44 (s, 1H), 2.38 (s, 3H). 625 CF.sub.3 [00701]embedded image (500 MHz, Chloroform-d) δ 9.26 (s, 1H), 8.82 (d, J = 5.5 Hz, 1H), 8.75 (d, J = 5.5 Hz, 1H), 7.26 (s, 1H), 5.59 (s, 1H). 626 CF.sub.3 [00702]embedded image (500 MHz, Chloroform-d) δ 9.19 (s, 1H), 8.88 (s, 1H), 7.28 (s, 1H). 627 CF.sub.3 [00703]embedded image (500 MHz, Chloroform-d) δ 8.82-8.66 (m, 2H), 7.31 (s, 1H), 6.92-6.81 (m, 1H), 5.93-5.84 (m, 2H). 628 CF.sub.3 [00704]embedded image (500 MHz, Chloroform-d) δ 9.45 (s, 2H), 7.29 (s, 1H), 5.39 (s, 1H). 629 CF.sub.3 [00705]embedded image (500 MHz, Chloroform-d) δ 9.46 (s, 1H), 7.25 (s, 1H), 5.85 (s, 1H), 3.93 (s, 3H). 630 CF.sub.3 [00706]embedded image (500 MHz, Chloroform-d) δ 7.05 (s, 1H), 5.87 (s, 1H), 2.82 (s, 6H). 631 CF.sub.3 [00707]embedded image 632 CF.sub.3 [00708]embedded image 633 CF.sub.3 [00709]embedded image 634 CF.sub.3 [00710]embedded image (500 MHz, Chloroform-d) δ 9.25 (d, J = 1.5 Hz, 1H), 8.53 (d, J = 7.5 Hz, 1H), 8.11-8.04 (m, 2H), 7.91-7.82 (m, 3H), 5.50 (s, 1H). 635 CF.sub.3 [00711]embedded image (500 MHz, Chloroform-d) δ 9.13 (s, 1H), 8.64-8.51 (m, 2H), 8.39 (d, J = 7.5 Hz, 1H), 8.05-7.96 (m, 2H), 6.86 (s, 1H). 636 CF.sub.3 [00712]embedded image (500 MHz, Chloroform-d) δ 9.08 (d, J = 1.5 Hz, 1H), 8.61 (d, J = 7.5 Hz, 1H), 8.06 (dd, J = 7.5, 1.5 Hz, 1H), 7.91- 7.83 (m, 2H), 7.78-7.69 (m, 2H), 5.36 (s, 1H). 637 CF.sub.3 [00713]embedded image (500 MHz, Chloroform-d) δ 9.34 (d, J = 1.4 Hz, 1H), 8.78 (s, 1H), 8.10 (s, 1H), 8.00 (dt, J = 7.5, 1.6 Hz, 1H), 7.81 (dd, J = 7.3, 1.6 Hz, 1H), 7.65-7.53 (m, 2H), 5.49 (s, 1H). 638 CF.sub.3 [00714]embedded image (500 MHz, Chloroform-d) δ 9.00 (d, J = 7.5 Hz, 1H), 8.78 (d, J = 7.5 Hz, 1H), 8.37 (d, J = 1.5 Hz, 1H), 8.12 (d, J = 1.5 Hz, 1H), 7.86 (s, 1H), 5.16 (s, 1H). 639 CF.sub.3 [00715]embedded image (500 MHz, Chloroform-d) δ 8.78-8.60 (m, 2H), 8.40 (d, J = 1.5 Hz, 1H), 8.27 (d, J = 7.5 Hz, 1H), 7.94 (dd, J = 7.5, 1.5 Hz, 1H), 7.89 (s, 1H), 5.46 (s, 1H). 640 CF.sub.3 [00716]embedded image (500 MHz, Chloroform-d) δ 9.68 (s, 1H), 8.25 (dd, J = 7.5, 1.5 Hz, 1H), 8.18- 8.11 (m, 3H), 7.74 (s, 1H). 641 CF.sub.3 [00717]embedded image (500 MHz, Chloroform-d) δ 8.92 (s, 1H), 8.40 (d, J = 1.5 Hz, 1H), 8.25 (d, J = 7.5 Hz, 1H), 7.92 (dd, J = 7.5, 1.5 Hz, 1H), 7.89 (s, 1H), 5.43 (s, 1H), 2.93 (q, J = 8.0 Hz, 2H), 1.27 (t, J = 8.0 Hz, 3H). 642 CF.sub.3 [00718]embedded image (500 MHz, Chloroform-d) δ 7.84 (s, 1H), 6.81 (dd, J = 7.5, 7.0 Hz, 1H), 6.66 (dd, J = 7.5, 2.0 Hz, 1H), 6.44 (dd, J = 7.0, 2.0 Hz, 1H), 5.20 (s, 1H), 4.24 (s, 1H), 3.04-2.89 (m, 4H), 2.15-2.07 (m, 2H). 643 CF.sub.3 [00719]embedded image (500 MHz, Chloroform-d) δ 7.85 (s, 1H), 7.14 (dd, J = 7.5, 2.0 Hz, 1H), 6.83 (d, J = 2.0 Hz, 1H), 6.67 (d, J = 7.5 Hz, 1H), 5.34 (s, 1H), 3.33-3.17 (m, 2H), 2.95-2.87 (m, 5H), 2.10-2.02 (m, 2H). 644 CF.sub.3 [00720]embedded image (500 MHz, Chloroform-d) δ 7.83 (s, 1H), 6.55-6.44 (m, 3H), 5.87 (s, 1H), 3.95 (s, 1H), 3.72-3.58 (m, 2H), 3.41- 3.25 (m, 2H), 2.99-2.87 (m, 1H), 1.88- 1.79 (m, 1H), 1.19-1.09 (m, 2H), 0.91-0.82 (m, 2H). 645 CF.sub.3 [00721]embedded image (500 MHz, Chloroform-d) δ 7.23-7.16 (m, 2H), 7.08-6.88 (m, 2H), 6.77 (s, 1H), 5.87 (s, 1H), 3.52-3.39 (m, 2H), 2.90-2.77 (m, 2H), 2.11-2.03 (m, 2H). 646 CF.sub.3 [00722]embedded image (500 MHz, Chloroform-d) δ 9.95-9.86 (m, 2H), 8.29 (dd, J = 2.5, 1.5 Hz, 1H), 8.15 (dd, J = 7.5, 1.5 Hz, 1H), 8.10 (d, J = 7.5 Hz, 1H), 7.86 (s, 1H), 5.70 (s, 1H). 647 CF.sub.3 [00723]embedded image (500 MHz, Chloroform-d) δ 9.95 (d, J = 1.5 Hz, 1H), 9.69 (s, 1H), 8.08-7.99 (m, 2H), 7.94 (d, J = 7.5 Hz, 1H), 7.89 (s, 1H), 5.46 (s, 1H). 648 CF.sub.3 [00724]embedded image (500 MHz, Chloroform-d) δ 8.10 (s, 1H), 8.05 (dd, J = 7.5, 1.5 Hz, 1H), 7.59 (d, J = 7.5 Hz, 1H), 6.74 (d, J = 1.5 Hz, 1H), 5.35 (s, 1H), 3.87 (s, 3H). 649 CF.sub.3 [00725]embedded image 650 CF.sub.3 [00726]embedded image 651 CF.sub.3 [00727]embedded image 652 CF.sub.3 [00728]embedded image 653 CF.sub.3 [00729]embedded image (500 MHz, Chloroform-d) δ 9.31 (d, J = 5.5 Hz, 1H), 8.28 (dd, J = 7.5, 1.5 Hz, 1H), 8.00 (d, J = 7.5 Hz, 1H), 7.90 (s, 1H), 7.87-7.76 (m, 2H), 5.50 (s, 1H). 654 CF.sub.3 [00730]embedded image (500 MHz, Chloroform-d) δ 9.33 (d, J = 7.5 Hz, 1H), 8.41 (d, J = 7.5 Hz, 1H), 8.10 (dd, J = 7.5, 1.5 Hz, 1H), 8.02 (d, J = 1.5 Hz, 1H), 7.94 (d, J = 7.5 Hz, 1H), 7.90 (s, 1H), 5.59 (s, 1H). 655 CF.sub.3 [00731]embedded image (500 MHz, Chloroform-d) δ 9.39 (d, J = 7.5 Hz, 1H), 9.01 (d, J = 1.5 Hz, 1H), 8.85 (s, 1H), 8.75 (d, J = 1.5 Hz, 1H), 8.62 (d, J = 7.5 Hz, 1H), 6.80 (s, 1H), 3.17 (s, 3H). 656 CF.sub.3 [00732]embedded image (500 MHz, Chloroform-d) δ 9.39 (s, 1H), 8.01-7.85 (m, 2H), 8.75-8.62 (m, 2H), 6.80 (s, 1H). 657 CF.sub.3 [00733]embedded image (500 MHz, Chloroform-d) δ 9.11 (s, 2H), 7.24 (s, 1H), 5.84 (s, 1H). 658 CF.sub.3 [00734]embedded image (500 MHz, Chloroform-d) δ 9.77 (s, 1H), 9.32 (s, 1H), 7.30 (s, 1H), 5.30 (s, 1H). 659 CF.sub.3 [00735]embedded image (500 MHz, Chloroform-d) δ 9.00 (s, 2H), 7.25 (s, 1H), 5.76 (s, 1H). 660 CF.sub.3 [00736]embedded image (500 MHz, Chloroform-d) δ 9.19 (s, 1H), 7.37 (s, 1H), 7.08 (s, 2H), 5.32 (s, 1H), 2.82 (s, 3H). 661 CF.sub.3 [00737]embedded image (500 MHz, Chloroform-d) δ 9.05 (s, 1H), 7.26 (s, 1H), 5.59 (s, 1H), 2.84 (s, 3H). 662 CF.sub.3 [00738]embedded image (500 MHz, Chloroform-d) δ 7.25 (s, 1H), 5.68 (s, 1H). 663 CF.sub.3 [00739]embedded image (500 MHz, Chloroform-d) δ 9.25 (s, 2H), 8.30 (s, 1H), 7.34 (s, 1H), 4.98 (s, 1H), 2.11 (s, 3H). 664 CF.sub.3 [00740]embedded image (500 MHz, Chloroform-d) δ 9.83 (s, 1H), 9.34 (s, 1H), 7.49 (s, 1H), 6.57 (s, 1H), 3.96 (s, 3H). 665 CF.sub.3 [00741]embedded image (500 MHz, Chloroform-d) δ 9.57 (s, 2H), 7.25 (s, 1H), 5.91 (s, 1H). 666 CF.sub.3 [00742]embedded image (500 MHz, Chloroform-d) δ 9.21 (s, 2H), 7.24 (s, 1H), 5.84 (s, 1H), 3.83 (s, 3H). 667 CF.sub.3 [00743]embedded image (500 MHz, Chloroform-d) δ 9.23 (s, 1H), 9.05 (s, 1H), 7.34 (s, 1H), 3.99 (s, 3H), 3.83 (s, 3H). 668 CF.sub.3 [00744]embedded image (500 MHz, Chloroform-d) δ 9.60 (s, 1H), 9.15 (d, J = 5.0 Hz, 1H), 7.86 (d, J = 5.0 Hz, 1H), 7.27 (s, 1H). 669 CF.sub.3 [00745]embedded image (500 MHz, Chloroform-d) δ 9.60 (s, 1H), 7.71 (s, 1H), 7.27 (s, 1H), 2.27 (q, J = 8.0 Hz, 2H), 1.19 (t, J = 8.0 Hz, 3H). 670 CF.sub.3 [00746]embedded image (500 MHz, Chloroform-d) δ 8.86 (d, J = 5.0 Hz, 1H), 7.52 (d, J = 5.0 Hz, 1H), 7.28 (s, 1H), 4.29 (q, J = 8.0 Hz, 2H), 1.29 (t, J = 8.0 Hz, 3H). 671 CF.sub.3 [00747]embedded image (500 MHz, Chloroform-d) δ 9.87 (s, 1H), 8.82 (s, 1H), 7.35 (s, 1H), 3.00 (s, 3H), 2.68 (s, 3H). 672 CF.sub.3 [00748]embedded image (500 MHz, Chloroform-d) δ 8.73 (s, 1H), 7.27 (s, 1H), 2.60 (s, 3H), 2.45 (s, 3H). 673 CF.sub.3 [00749]embedded image (500 MHz, Chloroform-d) δ 8.06 (s, 1H), 7.27 (s, 1H), 2.35 (s, 3H). 674 CF.sub.3 [00750]embedded image (500 MHz, Chloroform-d) δ 7.27 (s, 1H), 3.19 (s, 3H), 2.49 (s, 3H), 2.39 (s, 3H). 675 CF.sub.3 [00751]embedded image (500 MHz, Chloroform-d) δ 9.96 (s, 1H), 8.63 (s, 1H), 7.28 (s, 1H). 676 CF.sub.3 [00752]embedded image (500 MHz, Chloroform-d) δ 9.30 (s, 1H), 8.59 (s, 1H), 7.20 (s, 1H), 2.49 (s, 3H). 677 CF.sub.3 [00753]embedded image (500 MHz, Chloroform-d) δ 9.02 (d, J = 5.0 Hz, 2H), 7.47 (t, J = 5.0 Hz, 1H), 7.26 (s, 1H). 678 CF.sub.3 [00754]embedded image 679 CF.sub.3 [00755]embedded image (500 MHz, Chloroform-d) δ 7.26 (s, 1H), 6.51 (s, 1H), 2.67 (s, 3H). 680 CF.sub.3 [00756]embedded image (500 MHz, Chloroform-d) δ 8.05 (s, 1H), 7.26 (s, 1H), 3.47 (hept, J = 8.0 Hz, 1H), 2.66 (s, 3H), 1.47 (d, J = 8.0 Hz, 1H). 681 CF.sub.3 [00757]embedded image (500 MHz, Chloroform-d) δ 7.22 (s, 1H), 5.71 (s, 1H), 2.70 (s, 6H), 2.34 (s, 3H). 682 CF.sub.3 [00758]embedded image (500 MHz, Chloroform-d) δ 8.72 (s, 2H), 7.25 (s, 1H), 6.80 (s, 1H), 5.87 (s, 1H). 683 CF.sub.3 [00759]embedded image (500 MHz, Chloroform-d) δ 8.72 (s, 2H), 7.25 (s, 1H), 1.70-1.56 (m, 1H), 1.06-0.97 (m, 2H), 0.78-0.69 (m, 2H). 684 CF.sub.3 [00760]embedded image (500 MHz, Chloroform-d) δ 9.17 (d, J = 5.0 Hz, 1H), 8.06 (d, J = 5.0 Hz, 1H), 7.27 (s, 1H), 2.73 (q, J = 8.0 Hz, 2H), 1.34 (t, J = 8.0 Hz, 3H). 685 CF.sub.3 [00761]embedded image (500 MHz, Chloroform-d) δ 8.88 (d, J = 5.0 Hz, 1H), 7.88 (d, J = 5.0 Hz, 1H), 7.26 (s, 1H), 5.62-5.52 (m, 2H), 1.73- 1.44 (m, 3H). 686 CF.sub.3 [00762]embedded image 687 CF.sub.3 [00763]embedded image (500 MHz, Chloroform-d) δ 8.24 (s, 1H), 7.25 (s, 1H), 5.64 (s, 1H), 4.48 (s, 2H), 3.40 (s, 3H). 688 CF.sub.3 [00764]embedded image 689 CF.sub.3 [00765]embedded image (500 MHz, Chloroform-d) δ 8.96 (d, J = 5.0 Hz, 1H), 7.36-7.28 (m, 2H), 7.21 (d, J = 5.0 Hz, 1H), 6.90 (s, 1H), 6.45 (d, J = 2.5 Hz, 1H), 5.61 (dd, J = 2.5, 1.5 Hz, 1H). 690 CF.sub.3 [00766]embedded image (500 MHz, Chloroform-d) δ 9.94 (s, 1H), 9.47 (s, 1H), 8.95 (s, 1H), 7.45 (s, 1H), 5.98 (s, 1H), 3.44 (s, 2H), 2.78 (s, 3H). 691 CF.sub.3 [00767]embedded image (500 MHz, Chloroform-d) δ 9.49 (s, 1H), 7.39 (s, 1H), 7.24 (s, 1H), 5.77 (s, 1H), 5.10 (s, 2H), 2.66 (hept, J = 7.0 Hz, 1H), 1.18 (d, J = 7.0 Hz, 6H). 692 CF.sub.3 [00768]embedded image (500 MHz, Chloroform-d) δ 9.38 (s, 1H), 9.05 (s, 1H), 8.40 (s, 1H), 7.49 (s, 1H), 4.48 (s, 2H), 3.34 (s, 3H). 693 CF.sub.3 [00769]embedded image (500 MHz, Chloroform-d) δ 9.60 (d, J = 1.5 Hz, 1H), 7.71 (s, 1H), 7.24 (s, 1H), 5.72 (s, 1H), 3.62 (s, 2H), 2.68 (s, 6H). 694 CF.sub.3 [00770]embedded image (500 MHz, Chloroform-d) δ 9.19 (s, 2H), 7.29 (s, 1H), 5.40 (s, 1H), 4.66 (s, 2H), 3.60 (q, J = 8.0 Hz, 2H), 1.15 (t, J = 8.0 Hz, 3H). 695 CF.sub.3 [00771]embedded image (500 MHz, Chloroform-d) δ 9.12 (s, 1H), 9.05 (s, 1H), 7.26 (s, 1H), 6.48- 6.33 (m, 1H), 6.21 (s, 1H), 5.91-5.78 (m, 2H). 696 CF.sub.3 [00772]embedded image (500 MHz, Chloroform-d) δ 8.90 (d, J = 5.0 Hz, 1H), 8.11 (dd, J = 2.5, 2.0 Hz, 1H), 8.06-7.96 (m, 2H), 7.92 (t, J = 2.0 Hz, 1H), 7.28 (s, 1H). 697 CF.sub.3 [00773]embedded image 698 CF.sub.3 [00774]embedded image (500 MHz, Chloroform-d) δ 8.89 (d, J = 5.0 Hz, 1H), 7.59 (d, J = 5.0 Hz, 1H), 7.24 (s, 1H), 5.83 (s, 1H), 4.53 (s, 2H), 4.09 (s, 2H), 3.43 (s, 3H). 699 CF.sub.3 [00775]embedded image (500 MHz, Chloroform-d) δ 9.16 (s, 1H), 8.95 (s, 1H), 7.27 (s, 1H), 6.78 (s, 1H), 4.02-3.94 (m, 2H), 1.84-1.71 (m, 1H), 1.49-1.38 (m, 1H), 1.18- 1.00 (d, J = 6.8 Hz, 3H), 0.97-0.82 (m, 4H). 700 CF.sub.3 [00776]embedded image (500 MHz, Chloroform-d) δ 9.48 (s, 1H), 7.34 (s, 1H), 7.21 (s, 1H), 4.33 (t, J = 7.5 Hz, 2H), 3.64 (s, 3H), 2.67 (t, J = 7.5 Hz, 2H). 701 CF.sub.3 [00777]embedded image 702 CF.sub.3 [00778]embedded image (500 MHz, Chloroform-d) δ 7.77 (s, 1H), 7.25 (s, 1H), 5.89 (s, 1H), 3.72 (q, J = 8.0 Hz, 2H), 3.44 (s, 2H), 3.08 (s, 3H), 1.23 (t, J = 8.0 Hz, 3H). 703 CF.sub.3 [00779]embedded image (500 MHz, Chloroform-d) δ 8.98 (d, J = 5.0 Hz, 1H), 7.24-7.19 (m, 2H), 4.32 (s, 2H). 704 CF.sub.3 [00780]embedded image (500 MHz, Chloroform-d) δ 7.97 (s, 1H), 7.88 (s, 1H), 7.83 (s, 1H), 7.29 (s, 1H), 3.89 (s, 3H). 705 CF.sub.3 [00781]embedded image (500 MHz, Chloroform-d) δ 8.96 (s, 2H), 7.26 (s, 1H), 4.67 (s, 2H), 4.37 (s, 2H) 2.41 (s, 3H). 706 CF.sub.3 [00782]embedded image (500 MHz, Chloroform-d) δ 9.34 (s, 1H), 7.79 (s, 1H), 7.26 (s, 1H), 4.53 (s, 2H), 4.09 (s, 2H), 3.34 (s, 3H). 707 CF.sub.3 [00783]embedded image (500 MHz, Chloroform-d) δ 9.09 (s, 1H), 8.70 (d, J = 5.0 Hz, 2H), 7.64 (d, J = 5.0 Hz, 2H), 7.28 (s, 1H), 7.18 (s, 1H), 3.67 (q, J = 8.0 Hz, 2H), 1.34 (t, J = 8.0 Hz, 3H). 708 CF.sub.3 [00784]embedded image (500 MHz, Chloroform-d) δ 9.24 (s, 2H), 7.35 (s, 1H), 5.71 (s, 2H), 3.63 (s, 2H), 3.43 (s, 3H). 709 CF.sub.3 [00785]embedded image (500 MHz, Chloroform-d) δ 9.26 (d, J = 1.5 Hz, 1H), 8.43 (t, J = 1.5 Hz, 1H), 8.27-8.18 (m, 2H), 8.10 (s, 1H), 7.62- 7.48 (m, 2H), 5.74 (s, 1H), 2.10 (s, 3H). 710 CF.sub.3 [00786]embedded image (500 MHz, Chloroform-d) δ 9.06 (dd, J = 7.5, 1.5 Hz, 1H), 7.53-7.41 (m, 1H), 7.30-7.23 (m, 2H), 7.06 (s, 1H), 6.97 (d, J = 1.5 Hz, 1H), 6.02 (s, 2H), 5.53 (s, 1H), 3.30 (s, 3H). 711 CF.sub.3 [00787]embedded image (500 MHz, Chloroform-d) δ 8.17-8.14 (m, 2H), 7.78-7.68 (m, 3H), 7.55- 7.39 (m, 1H), 5.41 (s, 1H), 4.78 (s, 2H), 3.40 (s, 3H). 712 CF.sub.3 [00788]embedded image (500 MHz, Chloroform-d) δ 8.58 (d, J = 1.5 Hz, 1H), 8.34 (d, J = 7.5 Hz, 1H), 8.10 (dd, J = 7.5, 1.5 Hz, 1H), 7.56 (s, 1H), 7.04 (s, 1H), 5.72 (s, 1H). 713 CF.sub.3 [00789]embedded image 714 CF.sub.3 [00790]embedded image (500 MHz, Chloroform-d) δ 8.90 (dd, J = 7.5, 1.5 Hz, 1H), 8.36 (d, J = 7.5 Hz, 1H), 8.25-8.16 (m, 3H), 7.39-7.26 (m, 1H), 7.03 (s, 1H), 5.72 (s, 1H). 715 CF.sub.3 [00791]embedded image (500 MHz, Chloroform-d) δ 9.14 (d, J = 7.5 Hz, 1H), 8.17-8.14 (m, 2H), 7.76- 7.68 (m, 3H), 7.57-7.41 (m, 1H), 5.48 (s, 1H). 716 CF.sub.3 [00792]embedded image (500 MHz, Chloroform-d) δ 8.81 (dd, J = 7.5, 1.5 Hz, 1H), 8.19-8.10 (m, 2H), 7.93 (d, J = 1.5 Hz, 1H), 7.87 (s, 1H), 7.51 (dd, J = 7.5, 5.0 Hz, 1H), 5.47 (s, 1H), 5.30 (d, J = 73.5 Hz, 1H). 717 CF.sub.3 [00793]embedded image (500 MHz, Chloroform-d) δ 9.15 (dd, J = 7.5, 1.7 Hz, 1H), 8.88 (d, J = 1.5 Hz, 1H), 8.45-8.37 (m, 2H), 7.58 (dd, J = 7.5, 5.5 Hz, 1H), 6.99 (s, 1H). 718 CF.sub.3 [00794]embedded image (500 MHz, Chloroform-d) δ 8.84 (d, J = 7.5 Hz, 1H), 7.97-7.88 (m, 2H), 7.73 (dd, J = 7.5, 1.5 Hz, 1H), 7.51 (dd, J = 7.5, 7.0 Hz, 1H), 6.94 (dd, J = 7.5, 1.5 Hz, 1H), 5.70 (s, 1H), 3.29 (q, J = 8.0 Hz, 2H), 2.98 (s, 3H), 1.20 (t, J = 8.0 Hz, 3H). 719 CF.sub.3 [00795]embedded image 720 CF.sub.3 [00796]embedded image (500 MHz, Chloroform-d) δ 9.33 (d, J = 1.5 Hz, 1H), 8.50 (dd, J = 2.5, 1.5 Hz, 1H), 8.19 (d, J = 1.5 Hz, 1H), 8.04- 7.90 (m, 2H), 5.08 (s, 1H), 3.27 (s, 3H). 721 CF.sub.3 [00797]embedded image (500 MHz, Chloroform-d) δ 8.89 (d, J = 5.5 Hz, 1H), 8.15 (s, 1H), 7.87 (d, J = 1.5 Hz, 1H), 7.77 (d, J = 1.5 Hz, 1H), 7.12 (s, 1H), 6.85 (d, J = 5.5 Hz, 1H), 5.27-5.14 (m, 2H), 2.64 (s, 3H), 2.46 (s, 3H). 722 CF.sub.3 [00798]embedded image (500 MHz, Chloroform-d) δ 9.29 (d, J = 1.5 Hz, 1H), 8.99 (s, 1H), 8.74 (q, J = 1.5 Hz, 1H), 7.86-7.79 (m, 2H), 6.82 (s, 1H), 2.49 (s, 3H), 2.44 (s, 3H). 723 CF.sub.3 [00799]embedded image (500 MHz, Chloroform-d) δ 8.90 (d, J = 6.5 Hz, 1H), 8.35 (d, J = 1.5 Hz, 1H), 8.14 (dd, J = 6.5, 1.5 Hz, 1H), 7.94 (dd, J = 7.5, 1.5 Hz, 1H), 7.84 (dd, J = 7.5, 1.5 Hz, 1H), 7.38 (d, J = 7.5 Hz, 1H), 6.85 (s, 1H). 724 CF.sub.3 [00800]embedded image (500 MHz, Chloroform-d) δ 9.29 (d, J = 1.5 Hz, 1H), 8.38 (dd, J = 2.0, 1.5 Hz, 1H), 8.15 (dd, J = 7.5, 1.5 Hz, 1H), 8.13 (s, 1H), 7.88-7.70 (m, 2H), 7.54-7.41 (m, 1H), 5.43 (s, 1H). 725 CF.sub.3 [00801]embedded image (500 MHz, Chloroform-d) δ 8.92 (d, J = 5.5 Hz, 1H), 8.52 (d, J = 1.5 Hz, 1H), 8.35 (d, J = 5.5 Hz, 1H), 8.08 (dd, J = 7.5, 1.5 Hz, 1H), 7.50 (d, J = 7.5 Hz, 1H), 7.09 (s, 1H), 5.46 (s, 1H). 726 CF.sub.3 [00802]embedded image 727 CF.sub.3 [00803]embedded image (500 MHz, Chloroform-d) δ 9.42 (d, J = 1.5 Hz, 1H), 8.72 (d, J = 1.5 Hz, 1H), 8.37 (dd, J = 7.5, 1.5 Hz, 1H), 8.04 (dd, J = 7.5, 7.0 Hz, 1H), 7.94 (dd, J = 7.0, 1.5 Hz, 1H), 7.90 (s, 1H), 5.37 (s, 1H). 728 CF.sub.3 [00804]embedded image (500 MHz, Chloroform-d) δ 9.00 (s, 1H), 8.16-8.09 (m, 2H), 7.93 (d, J = 7.5 Hz, 1H), 7.66 (dd, J = 7.5, 7.0 Hz, 1H), 6.96 (s, 1H), 2.73-2.56 (m, 1H), 2.29-2.14 (m, 1H), 2.18-2.01 (m, 3H), 1.98-1.84 (m, 2H), 1.62-1.45 (m, 3H). 729 CF.sub.3 [00805]embedded image (500 MHz, Chloroform-d) δ 8.70 (d, J = 7.5 Hz, 1H), 8.44 (d, J = 1.5 Hz, 1H), 8.38 (s, 1H), 8.04 (s, 1H), 7.63 (dd, J = 7.5, 1.5 Hz, 1H), 3.95 (s, 3H). 730 CF.sub.3 [00806]embedded image (500 MHz, Chloroform-d) δ 8.70 (d, J = 1.5 Hz, 1H), 8.44-8.38 (m, 2H), 8.04 (s, 1H), 7.63 (dd, J = 7.5, 1.7 Hz, 1H), 3.95 (s, 3H). 731 CF.sub.3 [00807]embedded image (500 MHz, Chloroform-d) δ 8.52 (d, J = 7.5 Hz, 1H), 8.44 (dd, J = 7.5, 1.5 Hz, 1H), 8.14-8.08 (m, 2H), 8.03 (s, 1H), 7.69 (dd, J = 7.5, 1.5 Hz, 1H), 3.03 (s, 3H), 2.85 (s, 3H). 732 CF.sub.3 [00808]embedded image (500 MHz, Chloroform-d) δ 7.54-7.31 (m, 1H), 7.04-6.94 (m, 2H), 6.92- 6.71 (m, 1H), 5.50 (s, 1H). 733 CF.sub.3 [00809]embedded image .sup.1H NMR (500 MHz, DMSO-d6) δ 8.39- 8.31 (m, 1H), 8.21-8.18 (m, 1H), 7.55- 7.52 (m, 1H), 7.35 (s, 1H). 734 CF.sub.3 [00810]embedded image (500 MHz, Chloroform-d) δ 9.10 (dd, J = 7.5, 1.5 Hz, 1H), 8.29-8.16 (m, 2H), 7.99-7.72 (m, 2H), 7.52-7.39 (m, 1H), 7.17 (s, 1H). 735 CF.sub.3 [00811]embedded image (500 MHz, Chloroform-d) δ 7.35 (dd, J = 7.5, 7.0 Hz, 1H), 7.16 (dd, J = 7.5, 1.5 Hz, 1H), 7.09 (dd, J = 7.0, 1.5 Hz, 1H), 7.04 (s, 1H), 5.76 (s, 1H), 2.31 (s, 3H), 1.95-1.85 (m, 1H), 1.07-0.98 (m, 2H), 0.89-0.80 (m, 2H). 736 CF.sub.3 [00812]embedded image (500 MHz, Chloroform-d) δ 7.52 (dd, J = 11.0, 2.0 Hz, 1H), 7.44-7.21 (m, 1H), 7.30-7.25 (m, 2H), 7.07 (s, 1H), 5.50 (s, 1H). 737 CF.sub.3 [00813]embedded image (500 MHz, Chloroform-d) δ 7.61-7.52 (m, 2H), 7.48-7.40 (m, 2H), 7.04 (s, 1H), 5.69 (s, 1H). 738 CF.sub.3 [00814]embedded image (500 MHz, Chloroform-d) δ 7.68-7.61 (m, 2H), 7.00 (s, 1H), 6.75-6.68 (m, 2H), 5.76 (s, 1H), 4.56 (s, 2H). 739 CF.sub.3 [00815]embedded image (500 MHz, Chloroform-d) δ 7.47-7.37 (m, 4H), 7.07 (s, 1H), 5.48 (s, 1H). 740 CF.sub.3 [00816]embedded image (500 MHz, Chloroform-d) δ 7.62 (dd, J = 5.5, 2.0 Hz, 1H), 7.36-7.25 (m, 1H), 7.16 (dd, J = 11.0, 7.5 Hz, 1H), 7.01 (s, 1H), 5.81 (s, 1H). 741 CF.sub.3 [00817]embedded image (500 MHz, Chloroform-d) δ 7.30-7.23 (m, 2H), 7.10 (s, 1H), 5.62 (s, 1H), 3.89 (s, 3H). 742 CF.sub.3 [00818]embedded image (500 MHz, Chloroform-d) δ 7.94-7.74 (m, 2H), 7.67-7.55 (m, 2H), 7.07 (s, 1H), 5.49 (s, 1H). 743 CF.sub.3 [00819]embedded image (500 MHz, Chloroform-d) δ 9.38 (d, J = 1.5 Hz, 1H), 8.16 (d, J = 1.5 Hz, 1H), 7.98-7.92 (m, 2H), 7.64-7.51 (m, 2H), 7.15 (s, 1H). 744 CF.sub.3 [00820]embedded image (500 MHz, Chloroform-d) δ 7.45-7.25 (m, 2H), 7.18-7.05 (m, 1H), 7.01 (s, 1H), 5.81 (s, 1H). 745 CF.sub.3 [00821]embedded image (500 MHz, Chloroform-d) δ 7.50 (dd, J = 7.5, 5.5 Hz, 1H), 7.45 (dd, J = 11.0, 2.0 Hz, 1H), 7.24-7.11 (m, 1H), 7.01 (s, 1H), 5.80 (s, 1H). 746 CF.sub.3 [00822]embedded image (500 MHz, Chloroform-d) δ 7.73 (d, J = 7.5 Hz, 2H), 7.54 (d, J = 7.5 Hz, 2H), 7.07 (s, 1H), 5.48 (s, 1H). 747 CF.sub.3 [00823]embedded image (500 MHz, Chloroform-d) δ 7.37-7.33 (m, 1H), 7.25 (dd, J = 7.5, 1.5 Hz, 1H), 7.14 (d, J = 7.5 Hz, 1H), 7.06 (s, 1H), 5.57 (s, 1H), 2.30 (s, 3H), 2.20 (s, 3H). 748 CF.sub.3 [00824]embedded image (500 MHz, Chloroform-d) δ 7.32 (d, J = 1.5 Hz, 1H), 7.26-7.17 (m, 2H), 7.03 (s, 1H), 5.67 (s, 1H), 2.50 (s, 3H), 2.35 (s, 3H). 749 CF.sub.3 [00825]embedded image (500 MHz, Chloroform-d) δ 7.53 (d, J = 7.5 Hz, 2H), 7.42 (d, J = 7.5 Hz, 2H), 7.06 (s, 1H), 5.49 (s, 1H), 2.45 (s, 3H). 750 CF.sub.3 [00826]embedded image (500 MHz, Chloroform-d) δ 8.57 (dd, J = 2.0, 1.5 Hz, 1H), 8.27-8.16 (m, 1H), 7.95-7.71 (m, 2H), 7.03 (s, 1H), 5.85 (s, 1H). 751 CF.sub.3 [00827]embedded image (500 MHz, Chloroform-d) δ 7.76 (dd, J = 2.0, 1.5 Hz, 1H), 7.61-7.52 (m, 1H), 7.50-7.41 (m, 2H), 7.01 (s, 1H), 5.78 (s, 1H). 752 CF.sub.3 [00828]embedded image (500 MHz, Chloroform-d) δ 7.56-7.47 (m, 3H), 7.42-7.30 (m, 1H), 7.00 (s, 1H), 5.61 (s, 1H). 753 CF.sub.3 [00829]embedded image (500 MHz, Chloroform-d) δ 7.35 (d, J = 7.5 Hz, 1H), 7.20 (d, J = 7.5 Hz, 1H), 7.03 (s, 1H), 5.66 (s, 1H). 754 CF.sub.3 [00830]embedded image (500 MHz, Chloroform-d) δ 7.47 (d, J = 7.5 Hz, 2H), 7.09-7.03 (m, 3H), 5.49 (s, 1H), 4.00 (t, J = 7.5 Hz, 2H), 1.74- 1.50 (m, 4H), 1.04 (t, J = 8.0 Hz, 3H). 755 CF.sub.3 [00831]embedded image (500 MHz, Chloroform-d) δ 8.09 (d, J = 2.0 Hz, 1H), 7.92 (dd, J = 7.5, 2.0 Hz, 1H), 7.83 (d, J = 7.5 Hz, 1H), 7.05 (s, 1H), 5.49 (s, 1H). 756 CF.sub.3 [00832]embedded image (500 MHz, Chloroform-d) δ 8.13 (d, J = 1.5 Hz, 1H), 7.78-7.70 (m, 2H), 7.05 (s, 1H), 5.54 (s, 1H). 757 CF.sub.3 [00833]embedded image (500 MHz, Chloroform-d) δ 8.80 (d, J = 2.0 Hz, 1H), 8.62 (dd, J = 7.5, 2.0 Hz, 1H), 8.11 (d, J = 7.5 Hz, 1H), 7.01 (s, 1H), 5.69 (s, 1H). 758 CF.sub.3 [00834]embedded image (500 MHz, Chloroform-d) δ 8.06 (d, J = 2.0 Hz, 1H), 7.75 (dd, J = 7.5, 2.0 Hz, 1H), 7.17 (d, J = 7.5 Hz, 1H), 7.08 (s, 1H), 5.29 (s, 1H), 4.02 (s, 3H). 759 CF.sub.3 [00835]embedded image (500 MHz, Chloroform-d) δ 8.48 (s, 2H), 7.02 (s, 1H), 5.86 (s, 1H), 3.97 (s, 3H). 760 CF.sub.3 [00836]embedded image (500 MHz, Chloroform-d) δ 7.87 (d, J = 1.5 Hz, 1H), 7.56-7.50 (m, 2H), 6.99 (s, 1H), 5.62 (s, 1H), 2.48 (s, 3H). 761 CF.sub.3 [00837]embedded image (500 MHz, Chloroform-d) δ 7.70-7.63 (m, 2H), 7.20-7.07 (m, 2H), 5.43 (s, 1H). 762 CF.sub.3 [00838]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.75 (s, 1H), 9.34 (d, J = 2.0 Hz, 1H), 8.69 (dd, J = 8.0, 2.0 Hz, 1H), 8.09 (d, J = 8.0 Hz, 1H), 7.38 (s, 1H). 763 CF.sub.3 [00839]embedded image (500 MHz, Chloroform-d) δ 7.77 (d, J = 2.0 Hz, 1H), 7.49 (d, J = 7.5 Hz, 1H), 7.43 (dd, J = 7.5, 2.0 Hz, 1H), 7.04 (s, 1H), 5.65 (s, 1H). 764 CF.sub.3 [00840]embedded image (500 MHz, Chloroform-d) δ 7.43-7.36 (m, 1H), 7.35-7.23 (m, 2H), 7.01 (s, 1H), 5.69 (s, 1H). 765 CF.sub.3 [00841]embedded image (500 MHz, Chloroform-d) δ 7.33-7.22 (m, 3H), 7.01 (s, 1H), 6.85-6.69 (m, 1H), 5.79 (s, 1H), 3.87 (s, 3H). 766 CF.sub.3 [00842]embedded image (500 MHz, Chloroform-d) δ 7.37-7.23 (m, 1H), 7.22-7.11 (m, 2H), 7.12 (s, 1H), 5.50 (s, 1H). 767 CF.sub.3 [00843]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.44 (s, 1H), 8.78 (s, 1H), 8.47-8.35 (m, 1H), 7.99-7.87 (m, 1H), 7.30 (s, 1H), 3.88 (s, 3H). 768 CF.sub.3 [00844]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 12.27 (s, 1H), 8.99 (d, J = 2.0 Hz, 1H), 8.42 (dd, J = 8.5, 2.0 Hz, 1H), 7.61 (d, J = 8.5 Hz, 1H), 7.25 (s, 1H). 769 CF.sub.3 [00845]embedded image (500 MHz, Chloroform-d) δ 7.80 (d, J = 2.5 Hz, 1H), 7.61 (dd, J = 7.5, 2.5 Hz, 1H), 7.53 (d, J = 7.5 Hz, 1H), 7.01 (s, 1H), 5.66 (s, 1H). 770 CF.sub.3 [00846]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 12.25 (s, 1H), 9.07 (d, J = 2.0 Hz, 1H), 8.67 (d, J = 2.5 Hz, 1H), 8.41 (dd, J = 2.5, 2.0 Hz, 1H), 7.24 (s, 1H). 771 CF.sub.3 [00847]embedded image (500 MHz, Chloroform-d) δ 7.30 (d, J = 2.0 Hz, 1H), 7.22 (dd, J = 7.5, 2.0 Hz, 1H), 7.06-6.98 (m, 2H), 6.07 (s, 2H), 5.78 (s, 1H). 772 CF.sub.3 [00848]embedded image (500 MHz, Chloroform-d) δ 7.65 (dd, J = 7.5, 2.0 Hz, 1H), 7.46-7.29 (m, 3H), 7.05 (s, 1H), 5.66 (s, 1H). 773 CF.sub.3 [00849]embedded image 774 CF.sub.3 [00850]embedded image .sup.1H NMR (500 MHz, DMSO-d6) δ 13.27 (br, 1H), 5 7.61 (d, J = 1.5 Hz, 1H), 7.38 (s, 1H), 6.99 (d, J = 1.5 Hz, 1H), 4.09 (s, 3H). 775 CF.sub.3 [00851]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.38 (s, 1H), 7.07 (s, 1H), 6.70 (s, 1H), 3.86 (s, 3H). 776 CF.sub.3 [00852]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.19 (s, 1H), 7.15 (s, 1H), 6.87 (s, 1H), 3.90 (s, 3H). 777 CF.sub.3 [00853]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.40 (s, 1H), 7.34 (s, 1H), 6.97 (s, 1H), 3.87 (s, 3H). 778 CF.sub.3 [00854]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.38 (s, 1H), 7.37 (s, 1H), 6.80 (s, 1H), 3.76 (s, 3H). 779 CF.sub.3 [00855]embedded image .sup.1H NMR (500 MHz, DMSO-d6) δ 13.27 (br, 1H), 5 7.32 (s, 1H), 6.68 (s, 1H), 3.91 (s, 3H), 2.19 (s, 3H). 780 CF.sub.3 [00856]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 12.64 (s, 1H), 6.90 (s, 1H), 6.60 (s, 1H), 3.88 (s, 3H), 2.60 (q, J = 8.0 Hz, 2H), 1.19 (t, J = 8.0 Hz, 3H). 781 CF.sub.3 [00857]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.48 (s, 1H), 6.93 (s, 1H), 6.37 (s, 1H), 3.76 (s, 3H), 1.87-1.73 (m, 1H), 1.20-0.91 (m, 2H), 0.75-0.68 (m, 2H). 782 CF.sub.3 [00858]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.25 (s, 1H), 6.85 (s, 1H), 5.96 (s, 1H), 3.92 (s, 3H), 3.84 (s, 3H). 783 CF.sub.3 [00859]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.26 (s, 1H), 6.90 (s, 1H), 5.86 (s, 1H), 4.39 (q, J = 8.0 Hz, 2H), 3.89 (s, 3H), 1.36 (t, J = 8.0 Hz, 3H). 784 CF.sub.3 [00860]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 12.64 (s, 1H), 7.47-7.39 (m, 2H), 7.18-7.11 (m, 2H), 7.03-6.94 (m, 2H), 6.06 (s, 1H), 4.65 (s, 2 H), 3.83 (s, 3H). 785 CF.sub.3 [00861]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.23 (s, 1H), 7.21 (s, 1H), 6.86 (s, 1H), 3.88 (s, 3H), 3.55 (br, 2 H). 786 CF.sub.3 [00862]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 12.66 (s, 1H), 8.17 (s, 1H), 6.95 (s, 1H), 6.26 (s, 1H), 3.91 (s, 3H), 3.03 (s, 3H). 787 CF.sub.3 [00863]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.45 (s, 1H), 6.85 (s, 1H), 6.36 (s, 1H), 3.94 (s, 3H), 3.19 (s, 6H). 788 CF.sub.3 [00864]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.52 (s, 1H), 7.38 (s, 1H), 6.94 (s, 1H), 5.56 (s, 1H), 3.88 (s, 3H), 2.13 (s, 3H). 789 CF.sub.3 [00865]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.06 (s, 1H), 8.56 (s, 1H), 7.85 (s, 1H), 6.95 (s, 1H), 5.56 (s, 1H), 3.90 (s, 3H), 2.71 (s, 3H). 790 CF.sub.3 [00866]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ13.18 (s, 1H), 10.14 (s, 1H), 6.94 (s, 1H), 5.56 (s, 1H), 3.95 (s, 3H), 1.29 (s, 9H). 791 CF.sub.3 [00867]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 12.72 (s, 1H), 6.99 (s, 1H), 6.92 (s, 1H), 3.91 (s, 3H). 792 CF.sub.3 [00868]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.58 (s, 1H), 7.50 (s, 1H), 6.91 (s, 1H), 3.87 (s, 3H). 793 CF.sub.3 [00869]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.25 (s, 1H), 7.92-7.85 (m, 2H), 7.51-7.41 (m, 3H), 7.25 (s, 1H), 6.99 (s, 1H), 3.92 (s, 3H). 794 CF.sub.3 [00870]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.25 (s, 1H), 6.94 (t, J = 73.5 Hz, 1 H), 6.90 (s, 1H), 6.84 (s, 1H), 3.89 (s, 3H). 795 CF.sub.3 [00871]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ13.51 (s, 1H), 6.91 (s, 1H), 6.71 (s, 1H), 3.89 (s, 3H), 3.07 (s, 2H). 796 CF.sub.3 [00872]embedded image 797 CF.sub.3 [00873]embedded image 798 CF.sub.3 [00874]embedded image 799 CF.sub.3 [00875]embedded image 800 CF.sub.3 [00876]embedded image 801 CF.sub.3 [00877]embedded image 802 CF.sub.3 [00878]embedded image 803 CF.sub.3 [00879]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 12.78 (s, 1H), 7.37 (s, 1H), 3.76 (s, 3H), 2.70 (s, 3H). 804 CF.sub.3 [00880]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.48 (s, 1H), 7.50 (s, 1H), 6.37 (s, 1H), 3.76 (s, 3H). 805 CF.sub.3 [00881]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 12.59 (s, 1H), 7.87 (s, 1H), 6.89 (s, 1H), 3.88 (s, 3H). 806 CF.sub.3 [00882]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.42 (s, 1H), 8.12 (s, 1H), 6.90 (s, 1H), 3.86 (s, 3H). 807 CF.sub.3 [00883]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.38 (s, 1H), 7.60 (s, 1H), 6.37 (s, 1H), 3.76 (s, 3H). 808 CF.sub.3 [00884]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.40 (s, 1H), 7.56 (s, 1H), 6.88 (s, 1H), 3.85 (s, 3H), 2.08 (s, 3H). 809 CF.sub.3 [00885]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.38 (s, 1H), 7.67 (s, 1H), 6.89 (s, 1H), 3.84 (s, 3H), 2.70 (q, J = 8.0 Hz, 2H), 1.17 (t, J = 8.0 Hz, 3H). 810 CF.sub.3 [00886]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 12.68 (s, 1H), 7.76 (s, 1H), 6.37 (s, 1H), 3.76 (s, 3H), 2.41-2.28 (m, 1H), 1.12-1.02 (m, 2H), 0.82-0.72 (m, 2H). 811 CF.sub.3 [00887]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 12.78 (s, 1H), 7.19 (s, 1H), 6.90 (s, 1H), 3.90 (s, 3H), 3.80 (s, 3H). 812 CF.sub.3 [00888]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 12.87 (s, 1H), 7.19 (s, 1H), 6.90 (s, 1H), 4.10 (q, J = 8.0 Hz, 2H), 3.90 (s, 3H), 1.34 (t, J = 8.0 Hz, 3H). 813 CF.sub.3 [00889]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 12.78 (s, 1H), 7.50-7.44 (m, 2H), 7.41-7.27 (m, 4H), 6.95 (s, 1H), 5.15 (s, 2H), 3.91 (s, 3H). 814 CF.sub.3 [00890]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.03 (s, 1H), 7.70 (s, 1H), 6.86 (s, 1H), 5.83 (s, 2H), 3.89 (s, 3H). 815 CF.sub.3 [00891]embedded image 816 CF.sub.3 [00892]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.35 (s, 1H), 7.71 (s, 1H), 6.90 (s, 1H), 3.89 (s, 3H), 2.86 (s, 6H). 817 CF.sub.3 [00893]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.03 (s, 1 H) 9.96 (s, 1H), 7.87 (s, 1H), 6.95 (s, 1H), 3.92 (s, 3H), 2.07 (s, 3H). 818 CF.sub.3 [00894]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 12.66 (s, 1H), 8.60 (s, 1H), 7.87 (s, 1H), 6.97 (s, 1H), 6.16 (s, 1H), 3.93 (s, 3H), 2.68 (s, 3H). 819 CF.sub.3 [00895]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.35 (s, 1H), 9.78 (s, 1H), 7.87 (s, 1H), 6.95 (s, 1H), 3.92 (s, 3H), 1.49 (s, 9H). 820 CF.sub.3 [00896]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.21 (s, 1H), 7.92 (s, 1H), 6.92 (s, 1H), 3.87 (s, 3H). 821 CF.sub.3 [00897]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.45 (s, 1H), 8.27 (s, 1H), 6.89 (s, 1H), 3.89 (s, 3H). 822 CF.sub.3 [00898]embedded image 823 CF.sub.3 [00899]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.10 (s, 1H), 7.82 (s, 1H), 6.92 (s, 1H), 3.85 (s, 3H). 824 CF.sub.3 [00900]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.36 (s, 1H), 7.91 (s, 1H), 6.95 (s, 1H), 6.67 (t, J = 73.5 Hz, 1H), 3.83 (s, 3H). 825 CF.sub.3 [00901]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.16 (s, 1H), 7.77 (s, 1H), 6.93 (s, 1H), 3.83 (s, 3H), 3.07 (s, 2H). 826 CF.sub.3 [00902]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 12.89 (s, 1H), 7.61 (d, J = 2.5 Hz, 1H), 7.15 (s, 1H), 6.84 (d, J = 2.5 Hz, 1H), 3.68 (q, J = 8.0 Hz, 2H), 1.53 (t, J = 8.0 Hz, 3H). 827 CF.sub.3 [00903]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 12.78 (s, 1H), 7.16 (s, 1H), 6.37 (s, 1H), 4.08 (q, J = 8.0 Hz, 2H), 1.87-1.76 (m, 1H), 1.30 (t, J = 8.0 Hz, 3H), 1.12-0.88 (m, 2H), 0.71-0.63 (m, 2H). 828 CF.sub.3 [00904]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 12.57 (s, 1H), 7.60 (d, J = 2.0 Hz, 1H), 7.03 (s, 1H), 6.73 (d, J = 2.0 Hz, 1H), 4.15-3.82 (m, 1H), 1.26 (d, J = 6.5 Hz, 6H). 829 CF.sub.3 [00905]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 12.76 (s, 1H), 7.06 (s, 1H), 6.78 (s, 1H), 4.56- 4.23 (m, 1H), 2.39 (s, 3H), 1.26 (d, J = 4.5 Hz, 6H). 830 CF.sub.3 [00906]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.08 (s, 1H), 7.17 (d, J = 8.5 Hz, 1H), 6.50 (s, 1H), 4.46-4.09 (m, 1H), 1.40 (d, J = 4.5 Hz, 6H). 831 CF.sub.3 [00907]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ13.51 (s, 1H), 7.64 (d, J = 2.5 Hz, 1H), 6.91 (s, 1H), 6.68 (d, J = 2.5 Hz, 1H), 5.32 (s, 2H). 832 CF.sub.3 [00908]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ13.11 (s, 1H), 7.96 (d, J = 2.5 Hz, 1H), 7.65- 7.51 (m, 2H), 7.46-7.24 (m, 2H), 7.12- 7.01 (m, 2H), 6.83 (s, 1H). 833 CF.sub.3 [00909]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 12.63 (s, 1H), 7.64 (d, J = 2.0 Hz, 1H), 7.55- 7.15 (m, 2H), 7.32-7.24 (m, 1H), 7.22- 7.16 (m, 2H), 6.90 (s, 1H), 6.62 (d, J = 2.0 Hz, 1H), 5.46 (s, 2H). 834 CF.sub.3 [00910]embedded image .sup.1H NMR (500 MHz, Chloroform-d) δ 7.84 (d, J = 2.5 Hz, 1H), 7.21 (s, 1H), 6.68 (d, J = 2.5 Hz, 1H), 5.49 (s, 1H), 2.54 (s, 3H). 835 CF.sub.3 [00911]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ13.13 (s, 1H), 8.11 (d, J = 2.5 Hz, 1H), 6.97 (d, J = 2.5 Hz, 1H), 6.9O (s, 1H), 1.61 (s, 9H). 836 CF.sub.3 [00912]embedded image 837 CF.sub.3 [00913]embedded image 838 CF.sub.3 [00914]embedded image 839 CF.sub.3 [00915]embedded image .sup.1H NMR (500 MHz, DMSO-d6) δ 13.25 (s, 1H), 8.53 (s, 1H), 8.18 (s, 1H), 7.23 (s, 1H), 3.92 (s, 3H). 840 CF.sub.3 [00916]embedded image .sup.1H NMR (500 MHz, DMSO-d6) δ 12.83 (s, 1H), 8.56 (s, 1H), 8.20 (s, 1H), 7.20 (s, 1H), 4.22 (q, J = 7.2 Hz, 2H), 1.40 (t, J = 7.2 Hz, 3H). 841 CF.sub.3 [00917]embedded image 842 CF.sub.3 [00918]embedded image .sup.1H NMR (500 MHz, DMSO-d6) δ 12.66 (s, 1H), 8.44 (s, 1H), 7.22 (s, 1H), 3.83 (s, 3H), 3.31 (s, 3H). 843 CF.sub.3 [00919]embedded image 844 CF.sub.3 [00920]embedded image .sup.1H NMR (500 MHz, DMSO-d6) 13.52 (s, 1H), 8.99 (s, 1H), 8.50 (s, 1H), 7.92 (t, J = 58.5 Hz, 1H), 7.23 (s, 1H). 845 CF.sub.3 [00921]embedded image 846 CF.sub.3 [00922]embedded image .sup.1H NMR (500 MHz, DMSO-d6) δ 13.27 (br, 1H), 8.68 (s, 1H), 8.24 (s, 1H), 7.72- 6.70 (m, 6H), 5.43 (s, 2H). 847 CF.sub.3 [00923]embedded image 848 CF.sub.3 [00924]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 12.87 (s, 1H), 7.81 (s, 1H), 7.19 (s, 1H), 6.97 (s, 1H), 5.36 (t, J = 6.8 Hz, 1H), 3.90- 3.77 (m, 2H), 2.13-2.01 (m, 2H), 1.85- 1.68 (m, 2H), 1.67-1.50 (m, 2H). 849 CF.sub.3 [00925]embedded image 850 CF.sub.3 [00926]embedded image 851 CF.sub.3 [00927]embedded image 852 CF.sub.3 [00928]embedded image .sup.1H NMR (500 MHz, DMSO-d) δ 12.84 (s, 1H), 8.68 (s, 1H), 8.27 (s, 1H), 7.22 (s, 1H), 5.67 (q, J = 6.0 Hz, 1H), 3.45 (q, J = 7.0 Hz, 1H), 3.21 (dq, J = 14.2, 7.0 Hz, 1H), 1.62 (d, J = 6.0 Hz, 3H), 1.03 (t, J = 7.0 Hz, 3H). 853 CF.sub.3 [00929]embedded image 854 CF.sub.3 [00930]embedded image 855 CF.sub.3 [00931]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 12.54 (s, 1H), 7.72 (s, 1H), 7.45 (s, 1H), 6.87 (s, 1H), 3.68 (s, 3H). 856 CF.sub.3 [00932]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 12.93 (s, 1H), 7.40 (d, J = 2.5 Hz, 1H), 7.10 (d, J = 2.5 Hz, 1H), 6.87 (s, 1H), 3.94 (s, 3H). 857 CF.sub.3 [00933]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.24 (s, 1H), 7.75 (s, 1H), 7.58 (s, 1H), 6.91 (s, 1H), 3.79 (s, 3H). 858 CF.sub.3 [00934]embedded image 859 CF.sub.3 [00935]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.00 (s, 1H), 6.89 (s, 1H), 4.19 (s, 3H). 860 CF.sub.3 [00936]embedded image 861 CF.sub.3 [00937]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ13.13 (s, 1H), 8.26 (s, 1H), 8.00 (s, 1H), 6.88 (s, 1H). 862 CF.sub.3 [00938]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 12.60 (s, 1H), 8.23 (d, J = 2.0 Hz, 1H), 7.41 (d, J = 2.0 Hz, 1H), 6.89 (s, 1H). 863 CF.sub.3 [00939]embedded image .sup.1H NMR (500 MHz, DMSO-d6) δ 12.86 (br, 1H), 7.26 (s, 1H), 2.38 (s, 3H), 2.20 (s, 3H). 864 CF.sub.3 [00940]embedded image 865 CF.sub.3 [00941]embedded image 866 CF.sub.3 [00942]embedded image 867 CF.sub.3 [00943]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 12.66 (s, 1H), 8.05 (d, J = 2.5 Hz, 1H), 7.56 (d, J = 2.5 Hz, 1H), 6.88 (s, 1H). 868 CF.sub.3 [00944]embedded image 869 CF.sub.3 [00945]embedded image 870 CF.sub.3 [00946]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 12.83 (s, 1H), 9.24 (s, 1H), 8.24 (s, 1H), 6.89 (s, 1H). 871 CF.sub.3 [00947]embedded image 872 CF.sub.3 [00948]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 12.70 (s, 1H), 7.94 (s, 1H), 6.84 (s, 1H). 873 CF.sub.3 [00949]embedded image .sup.1H NMR (500 MHz, DMSO-d6) δ 13.26 (br, 1H), 7.35 (s, 1H), 7.29 (s, 1H), 4.08 (s, 3H). 874 CF.sub.3 [00950]embedded image 875 CF.sub.3 [00951]embedded image 876 CF.sub.3 [00952]embedded image .sup.1H NMR (500 MHz, DMSO-d6) δ 13.86 (s, 1H), 9.07 (s, 1H), 8.50 (d, J = 6.5 Hz, 1H), 7.70 (d, J = 7.5 Hz, 1H), 7.50- 7.34 (m, 2H), 7.21 (s, 1H). 877 CF.sub.3 [00953]embedded image .sup.1H NMR (500 MHz, DMSO-d6) δ 12.91 (s, 1H), 7.63 (d, J = 8.0 Hz, 1H), 7.54 (s, 1H), 7.51 (d, J = 8.0 Hz, 1H), 7.25 (s, 1H), 7.17 (m, 1H), 7.00 (m, 1H). 878 CF.sub.3 [00954]embedded image 879 CF.sub.3 [00955]embedded image 880 CF.sub.3 [00956]embedded image 881 CF.sub.3 [00957]embedded image 882 CF.sub.3 [00958]embedded image 883 CF.sub.3 [00959]embedded image 884 CF.sub.3 [00960]embedded image 885 CF.sub.3 [00961]embedded image 886 CF.sub.3 [00962]embedded image 887 CF.sub.3 [00963]embedded image 888 CF.sub.3 [00964]embedded image 889 CF.sub.3 [00965]embedded image 890 CF.sub.3 [00966]embedded image 891 CF.sub.3 [00967]embedded image 892 CF.sub.3 [00968]embedded image 893 CF.sub.3 [00969]embedded image 894 CF.sub.3 [00970]embedded image 895 CF.sub.3 [00971]embedded image 896 CF.sub.3 [00972]embedded image 897 CF.sub.3 [00973]embedded image 898 CF.sub.3 [00974]embedded image 899 CF.sub.3 [00975]embedded image 900 CF.sub.3 [00976]embedded image 901 CF.sub.3 [00977]embedded image 902 CF.sub.3 [00978]embedded image 903 CF.sub.3 [00979]embedded image 904 CF.sub.3 [00980]embedded image 905 CF.sub.3 [00981]embedded image 906 CF.sub.3 [00982]embedded image 907 CF.sub.3 [00983]embedded image 908 CF.sub.3 [00984]embedded image 909 CF.sub.3 [00985]embedded image 910 CF.sub.3 [00986]embedded image 911 CF.sub.3 [00987]embedded image 912 CF.sub.3 [00988]embedded image 913 CF.sub.3 [00989]embedded image 914 CF.sub.3 [00990]embedded image 915 CF.sub.3 [00991]embedded image 916 CF.sub.3 [00992]embedded image 917 CF.sub.3 [00993]embedded image 918 CF.sub.3 [00994]embedded image 919 CF.sub.3 [00995]embedded image 920 CF.sub.3 [00996]embedded image 921 CF.sub.3 [00997]embedded image 922 CF.sub.3 [00998]embedded image 923 CF.sub.3 [00999]embedded image 924 CF.sub.3 [01000]embedded image 925 CF.sub.3 [01001]embedded image 926 CF.sub.3 [01002]embedded image 927 CF.sub.3 [01003]embedded image 928 CF.sub.3 [01004]embedded image 929 CF.sub.3 [01005]embedded image 930 CF.sub.3 [01006]embedded image 931 CF.sub.3 [01007]embedded image 932 CF.sub.3 [01008]embedded image 933 CF.sub.3 [01009]embedded image 934 CF.sub.3 [01010]embedded image 935 CF.sub.3 [01011]embedded image 936 CF.sub.3 [01012]embedded image 937 CF.sub.3 [01013]embedded image 938 CF.sub.3 [01014]embedded image 939 CF.sub.3 [01015]embedded image 940 CF.sub.3 [01016]embedded image 941 CF.sub.3 [01017]embedded image 942 CF.sub.3 [01018]embedded image 943 CF.sub.3 [01019]embedded image 944 CF.sub.3 [01020]embedded image 945 CF.sub.3 [01021]embedded image 946 CF.sub.3 [01022]embedded image 947 CF.sub.3 [01023]embedded image 948 CF.sub.3 [01024]embedded image 949 CF.sub.3 [01025]embedded image 950 CF.sub.3 [01026]embedded image 951 CF.sub.3 [01027]embedded image 952 CF.sub.3 [01028]embedded image 953 CF.sub.3 [01029]embedded image 954 CF.sub.3 [01030]embedded image 955 CF.sub.3 [01031]embedded image 956 CF.sub.3 [01032]embedded image 957 CF.sub.3 [01033]embedded image 958 CF.sub.3 [01034]embedded image 959 CF.sub.3 [01035]embedded image 960 CF.sub.3 [01036]embedded image 961 CF.sub.3 [01037]embedded image 962 CF.sub.3 [01038]embedded image 963 CF.sub.3 [01039]embedded image .sup.1H NMR (500 MHz, DMSO-d6) δ 12.59 (s, 1H), 8.66 (d, J = 1.5 Hz, 1H), 8.36 (dd, J = 8.0, 1.5 Hz, 1H), 7.66 (m, 1H), 7.24 (s, 1H). 964 CF.sub.3 [01040]embedded image .sup.1H NMR (500 MHz, DMSO-d6) δ 12.67 (s, 1H), 8.84 (d, J = 5.0 Hz, 1H), 8.58 (m, 1H), 7.23 (s, 1H), 7.17 (dd, J = 8.0, 5.0 Hz, 1H). 965 CF.sub.3 [01041]embedded image .sup.1H NMR (500 MHz, DMSO-d6) δ 12.98 (s, 1H), 8.46 (dd, J = 5.0, 1.5 Hz, 1H), 7.99 (dd, J = 8.0, 1.5 Hz, 1H), 7.61 (dd, J = 8.1, 5.0 Hz, 1H), 7.28 (s, 1H). 966 CF.sub.3 [01042]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.62 (s, 1H), 8.99 (d, J = 2.5 Hz, 1H), 8.34 (dd, J = 8.5, 2.5 Hz, 1H), 7.81 (d, J = 8.5 Hz, 1H), 7.3O (s, 1H). 967 CF.sub.3 [01043]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.73 (s, 1H), 9.14 (s, 1H), 8.82 (s, 1H), 8.59 (s, 1H), 7.32 (s, 1H). 968 CF.sub.3 [01044]embedded image .sup.1H NMR (500 MHz, DMSO-d6) δ 12.66 (s, 1H), 8.82 (s, 1H), 8.56 (d, J = 5.0 Hz, 1H), 7.68 (d, J = 5.0 Hz, 1H), 7.28 (s, 1H) 969 CF.sub.3 [01045]embedded image .sup.1H NMR (500 MHz, DMSO-d6) δ 13.12 (s, 1H), 8.26 (dd, J = 5.0, 1.5 Hz, 1H), 7.77 (dd, J = 8.0, 1.5 Hz, 1H), 7.50 (dd, J = 8.0, 5.0 Hz, 1H), 7.26 (s, 1H). 970 CF.sub.3 [01046]embedded image .sup.1H NMR (500 MHz, DMSO-d6) δ 12.87 (s, 1H), 8.59 (d, J = 1.0 Hz, 1H), 7.82 (d, J = 7.5 Hz, 1H), 7.70 (dd, J = 7.5, 1.0 Hz, 1H), 7.28 (s, 1H) 971 CF.sub.3 [01047]embedded image .sup.1H NMR (500 MHz, DMSO-d6) δ 13.17 (s, 1H), 8.99 (d, J = 1.0 Hz, 1H), 8.87 (d, J = 1.0 Hz, 1H), 8.31 (s, 1H), 7.23 (s, 1H). 972 CF.sub.3 [01048]embedded image .sup.1H NMR (500 MHz, DMSO-d6) δ 12.97 (s, 1H), 8.61 (s, 1H), 8.32 (d, J = 5.0 Hz, 1H), 7.80 (d, J = 5.0 Hz, 1H), 7.29 (s, 1H). 973 CF.sub.3 [01049]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ13.62 (s, 1H), 8.55 (dd, J = 5.0, 1.5 Hz, 1H), 7.76 (dd, J = 7.5, 1.5 Hz, 1H), 7.35 (dd, J = 7.5, 5.0 Hz, 1H), 7.30 (s, 1H), 2.32 (s, 3H). 974 CF.sub.3 [01050]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.41 (s, 1H), 9.07 (d, J = 2.0 Hz, 1H), 8.30 (dd, J = 8.0, 2.0 Hz, 1H), 7.41 (d, J = 8.0 Hz, 1H), 7.26 (s, 1H), 2.54 (s, 3H). 975 CF.sub.3 [01051]embedded image .sup.1H NMR (500 MHz, Chloroform-d) δ 8.73 (s, 1H), 8.61 (d, J = 5.0 Hz, 1H), 7.26 (d, J = 5.0 Hz, 1H), 6.94 (s, 1H), 5.64 (s, 1H), 2.36 (s, 3H). 976 CF.sub.3 [01052]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.78 (s, 1H), 8.93-8.92 (m, 1H), 8.49-8.45 (m, 1H), 8.34-8.33 (m, 1H), 7.35 (s, 1H). 977 CF.sub.3 [01053]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.65 (s, 1H), 9.44 (s, 1H), 9.10 (s, 1H), 8.75 (s, 1H), 7.33 (s, 1H). 978 CF.sub.3 [01054]embedded image .sup.1H NMR (500 MHz, DMSO-d6) δ 12.88 (s, 1H), 8.85 (s, 1H), 8.70 (d, J = 5.0 Hz, 1H), 7.58-7.53 (m, 1H), 7.28 (s, 1H). 979 CF.sub.3 [01055]embedded image .sup.1H NMR (500 MHz, DMSO-d6) δ 13.37 (s, 1H), 8.85 (dd, J = 5.0, 1.5 Hz, 1H), 8.22 (dd, J = 8.1, 1.5 Hz, 1H), 7.92 (dd, J = 7.9, 5.0 Hz, 1H), 7.28 (s, 1H). 980 CF.sub.3 [01056]embedded image .sup.1H NMR (500 MHz, DMSO-d6) δ 13.27 (s, 1H), 9.09 (s, 1H), 8.88 (d, J = 5.0 Hz, 1H), 7.86 (d, J = 5.0 Hz, 1H), 7.25 (s, 1H). 981 CF.sub.3 [01057]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 8.84 (d, J = 2.5 Hz, 1H), 8.22 (dd, J = 8.5, 2.5 Hz, 1H), 7.16 (s, 1H), 6.76 (s, 2H), 6.62 (d, J = 8.5 Hz, 1H). 982 CF.sub.3 [01058]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 8.47 (s, 1H), 7.99 (s, 1H), 7.75 (s, 1H), 7.15 (s, 1H). 983 CF.sub.3 [01059]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.53 (s, 1H), 9.31 (d, J = 2.0 Hz, 1H), 8.63 (dd, J = 8.0, 2.0 Hz, 1H), 8.18 (d, J = 8.0 Hz, 1H), 7.33 (s, 1H). 984 CF.sub.3 [01060]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.84 (s, 1H), 9.40 (s, 1H), 9.14 (s, 1H), 8.84 (s, 1H), 7.34 (s, 1H). 985 CF.sub.3 [01061]embedded image 986 CF.sub.3 [01062]embedded image .sup.1H NMR (500 MHz, DMSO-d6) δ 13.02 (s, 1H), 8.43-8.35 (dd, J = 8.0, 1.0 Hz, 1H), 7.84-7.81 (m, 1H), 7.24 (s, 1H). 987 CF.sub.3 [01063]embedded image .sup.1H NMR (500 MHz, DMSO-d6) δ 13.22 (s, 1H), 8.45-8.41 (m, 1H), 7.25-7.18 (m, 2H). 988 CF.sub.3 [01064]embedded image .sup.1H NMR (500 MHz, DMSO-d6) δ 13.14 (s, 1H), 8.58-8.43 (m, 1H), 7.91-7.88 (m, 1H), 7.24 (s, 1H). 989 CF.sub.3 [01065]embedded image .sup.1H NMR (500 MHz, DMSO-d6) δ 13.02 (s, 1H), 8.76-8.63 (m, 1H), 7.24 (s, 1H), 7.01 (m, 1H). 990 CF.sub.3 [01066]embedded image .sup.1H NMR (500 MHz, DMSO-d6) δ 13.22 (s, 1H), 8.66-8.42 (m, 1H), 8.35-8.23 (m, 1H), 7.36 (s, 1H). 991 CF.sub.3 [01067]embedded image .sup.1H NMR (500 MHz, DMSO-d6) δ 13.15 (s, 1H), 8.16 (d, J = 8.0 Hz, 1H), 7.43 (d, J = 8.0 Hz, 1H), 7.24 (s, 1H). 992 CF.sub.3 [01068]embedded image .sup.1H NMR (500 MHz, DMSO-d6) δ 13.01 (s, 1H), 8.60 (d, J = 1.5 Hz, 1H), 8.12 (d, J = 1.5 Hz, 1H), 7.24 (s, 1H). 993 CF.sub.3 [01069]embedded image .sup.1H NMR (500 MHz, DMSO-d6) δ 13.08 (s, 1H), 8.59 (d, J = 5.0 Hz, 1H), 7.59 (d, J = 5.0 Hz, 1H), 7.24 (s, 1H). 994 CF.sub.3 [01070]embedded image .sup.1H NMR (500 MHz, DMSO-d6) δ 12.99 (s, 1H), 8.95 (d, J = 1.5 Hz, 1H), 8.23 (d, J = 1.5 Hz, 1H), 7.24 (s, 1H). 995 CF.sub.3 [01071]embedded image .sup.1H NMR (500 MHz, DMSO-d6) δ 13.41 (s, 1H), 8.88 (s, 1H), 7.68 (s, 1H), 7.24 (s, 1H). 996 CF.sub.3 [01072]embedded image .sup.1H NMR (500 MHz, DMSO-d6) δ 13.25 (s, 1H), 8.77 (d, J = 1.5 Hz, 1H), 8.49 (d, J = 1.5 Hz, 1H), 7.24 (s, 1H). 997 CF.sub.3 [01073]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.38 (s, 1H), 8.29 (dd, J = 8.5, 7.5 Hz, 1H), 7.71 (d, J = 7.5 Hz, 1H), 7.36 (s, 1H). 998 CF.sub.3 [01074]embedded image .sup.1H NMR (500 MHz, DMSO-d6) δ 13.31 (s, 1H), 8.43 (dd, J = 7.5, 1.0 Hz, 1H), 8.21 (dd, J = 5.0, 1.0 Hz, 1H), 7.24 (s, 1H). 999 CF.sub.3 [01075]embedded image .sup.1H NMR (500 MHz, DMSO-d6) δ 13.22 (s, 1H), 8.42 (dd, J = 6.0, 5.0 Hz, 1H), 7.50 (d, J = 5.0 Hz, 1H), 7.23 (s, 1H). 1000 CF.sub.3 [01076]embedded image .sup.1H NMR (500 MHz, DMSO-d6) δ 13.45 (s, 1H), 8.79 (dd, J = 6.5, 1.0 Hz, 1H), 8.30 (dd, J = 5.0, 1.0 Hz, 1H), 7.24 (s, 1H). 1001 CF.sub.3 [01077]embedded image .sup.1H NMR (500 MHz, DMSO-d6) δ 12.88 (s, 1H), 8.71 (d, J = 5.5 Hz, 1H), 7.31 (d, J = 7.5 Hz, 1H), 7.24 (s, 1H). 1002 CF.sub.3 [01078]embedded image .sup.1H NMR (500 MHz, DMSO-d6) δ 13.13 (s, 1H), 8.55 (s, 1H), 8.36 (d, J = 8.0 Hz, 1H), 7.24 (s, 1H). 1003 CF.sub.3 [01079]embedded image .sup.1H NMR (500 MHz, DMSO-d6) δ 13.17 (s, 1H), 8.27 (dd, J = 8.0, 5.0 Hz, 1H), 7.24 (s, 1H), 7.07 (dd, J = 9.5, 8.0 Hz, 1H). 1004 CF.sub.3 [01080]embedded image .sup.1H NMR (500 MHz, DMSO-d6) δ 13.05 (s, 1H), 8.60 (dd, J = 8.0, 1.0 Hz, 1H), 7.74 (dd, J = 5.5, 1.0 Hz, 1H), 7.24 (s, 1H). 1005 CF.sub.3 [01081]embedded image .sup.1H NMR (500 MHz, DMSO-d6) δ 13.09 (s, 1H), 8.62 (dd, J = 6.5, 5.0 Hz, 1H), 7.30 (dd, J = 8.0, 5.0 Hz, 1H), 7.23 (s, 1H). 1006 CF.sub.3 [01082]embedded image .sup.1H NMR (500 MHz, DMSO-d6) δ 13.18 (s, 1H), 8.75 (d, J = 1.0 Hz, 1H), 7.83 (dd, J = 8.0, 1.0 Hz, 1H), 7.24 (s, 1H). 1007 CF.sub.3 [01083]embedded image .sup.1H NMR (500 MHz, DMSO-d6) δ 13.27 (s, 1H), 8.93 (d, J = 5.0 Hz, 1H), 7.38 (d, J = 8.0 Hz, 1H), 7.23 (s, 1H). 1008 CF.sub.3 [01084]embedded image .sup.1H NMR (500 MHz, DMSO-d6) δ 12.57 (s, 1H), 8.88 (d, J = 5.0 Hz, 1H), 8.47 (d, J = 4.0 Hz, 1H), 7.36 (s, 1H). 1009 CF.sub.3 [01085]embedded image 1010 CF.sub.3 [01086]embedded image 1011 CF.sub.3 [01087]embedded image 1012 CF.sub.3 [01088]embedded image 1013 CF.sub.3 [01089]embedded image 1014 CF.sub.3 [01090]embedded image 1015 CF.sub.3 [01091]embedded image 1016 CF.sub.3 [01092]embedded image 1017 CF.sub.3 [01093]embedded image 1018 CF.sub.3 [01094]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.15 (s, 1H), 8.36 (s, 1H), 7.57 (s, 1H), 7.34 (s, 1H), 2.20 (s, 3H). 1019 CF.sub.3 [01095]embedded image 1020 CF.sub.3 [01096]embedded image 1021 CF.sub.3 [01097]embedded image 1022 CF.sub.3 [01098]embedded image 1023 CF.sub.3 [01099]embedded image 1024 CF.sub.3 [01100]embedded image 1025 CF.sub.3 [01101]embedded image 1026 CF.sub.3 [01102]embedded image 1027 CF.sub.3 [01103]embedded image 1028 CF.sub.3 [01104]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 12.70 (s, 1H), 8.14 (d, J = 2.0 Hz, 1H), 7.58 (d, J = 2.0 Hz, 1H), 7.24 (s, 1H), 5.18 (s, 2H), 3.91 (s, 3H). 1029 CF.sub.3 [01105]embedded image 1030 CF.sub.3 [01106]embedded image 1031 CF.sub.3 [01107]embedded image 1032 CF.sub.3 [01108]embedded image 1033 CF.sub.3 [01109]embedded image 1034 CF.sub.3 [01110]embedded image 1035 CF.sub.3 [01111]embedded image 1036 CF.sub.3 [01112]embedded image 1037 CF.sub.3 [01113]embedded image 1038 CF.sub.3 [01114]embedded image 1039 CF.sub.3 [01115]embedded image 1040 CF.sub.3 [01116]embedded image 1041 CF.sub.3 [01117]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.13 (s, 1H), 8.89 (d, J = 2.5 Hz, 1H), 8.24 (dd, J = 9.0, 2.5 Hz, 1H), 7.19 (s, 1H), 6.94 (d, J = 9.0 Hz, 1H), 3.65-3.55 (m, 4H), 3.42 (s, 4H), 1.41 (s, 9H). 1042 CF.sub.3 [01118]embedded image 1043 CF.sub.3 [01119]embedded image 1044 CF.sub.3 [01120]embedded image 1045 CF.sub.3 [01121]embedded image 1046 CF.sub.3 [01122]embedded image 1047 CF.sub.3 [01123]embedded image 1048 CF.sub.3 [01124]embedded image 1049 CF.sub.3 [01125]embedded image 1050 CF.sub.3 [01126]embedded image 1051 CF.sub.3 [01127]embedded image 1052 CF.sub.3 [01128]embedded image 1053 CF.sub.3 [01129]embedded image 1054 CF.sub.3 [01130]embedded image 1055 CF.sub.3 [01131]embedded image 1056 CF.sub.3 [01132]embedded image 1057 CF.sub.3 [01133]embedded image 1058 CF.sub.3 [01134]embedded image 1059 CF.sub.3 [01135]embedded image 1060 CF.sub.3 [01136]embedded image 1061 CF.sub.3 [01137]embedded image 1062 CF.sub.3 [01138]embedded image 1063 CF.sub.3 [01139]embedded image 1064 CF.sub.3 [01140]embedded image 1065 CF.sub.3 [01141]embedded image 1066 CF.sub.3 [01142]embedded image 1067 CF.sub.3 [01143]embedded image 1068 CF.sub.3 [01144]embedded image 1069 CF.sub.3 [01145]embedded image 1070 CF.sub.2CF.sub.3 [01146]embedded image 1071 CF.sub.2CF.sub.3 [01147]embedded image 1072 CF.sub.2CF.sub.3 [01148]embedded image 1073 CH.sub.2F [01149]embedded image 1074 CH.sub.2F [01150]embedded image 1075 CH.sub.2F [01151]embedded image 1076 CH.sub.2F [01152]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.15 (s, 1H), 8.43-8.33 (m, 1H), 7.99-7.80 (m, 1H), 7.74-7.55 (m, 1H), 6.95 (s, 1H), 5.40 (d, J = 65.0 Hz, 2H). 1077 CH.sub.2F [01153]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.18 (s, 1H), 8.73 (dd, J = 4.5, 1.5 Hz, 1H), 7.80-7.71 (m, 2H), 6.96 (s, 1H), 5.40 (d, J = 65.0 Hz, 2H), 1.87-1.81 (m, 1H), 0.77-0.65 (m, 2H), 0.62-0.55 (m, 2H). 1078 CH.sub.2F [01154]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.00 (s, 1H), 8.47 (dd, J = 5.5, 1.0 Hz, 1H), 8.14 (dd, J = 7.0, 1.0 Hz, 1H), 7.04 (s, 1H), 5.40 (d, J = 65.0 Hz, 2H), 3.07 (q, J = 9.0 Hz, 2H). 1079 CH.sub.2F [01155]embedded image 1080 CH.sub.2F [01156]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.18 (s, 1H), 8.26 (dd, J = 8.0, 5.0 Hz, 1H), 7.82 (d, J = 8.0 Hz, 1H), 6.96 (s, 1H), 6.60 (t, J = 73.5 Hz, 1H), 5.30 (s, 1H). 1081 CF.sub.2CF.sub.3 [01157]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.05 (s, 1H), 8.43-8.35 (m, 1H), 8.04-7.90 (m, 1H), 7.75-7.61 (m, 1H), 7.00 (s, 1H). 1082 CF.sub.2CF.sub.3 [01158]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 12.97 (s, 1H), 9.16 (d, J = 1.5 Hz, 1H), 8.18 (dd, J = 8.0, 1.5 Hz, 1H), 7.74 (d, J = 8.0 Hz, 1H), 6.96 (s, 1H), 3.00 (d, J = 7.0 Hz, 2H), 1.73-1.52 (m, 4H), 1.56- 1.37 (m, 2H), 1.33-1.14 (m, 5H). 1083 CF.sub.2CF.sub.3 [01159]embedded image .sup.1H NMR (500 MHz, DMSO-d.sub.6) δ 13.14 (s, 1H), 8.81 (s, 1H), 6.89 (s, 1H), 2.98 (t, J = 7.5 Hz, 2H), 1.70-1.55 (m, 2H), 0.92 (t, J = 8.0 Hz, 3H). 1084 CH.sub.2F [01160]embedded image 1085 CHF.sub.2 [01161]embedded image 1086 CHF.sub.2 [01162]embedded image 1087 CH.sub.2F [01163]embedded image 1088 CH.sub.2F [01164]embedded image 1089 CHF.sub.2 [01165]embedded image 1090 CHF.sub.2 [01166]embedded image 1091 CHF.sub.2 [01167]embedded image 1092 CF.sub.2CF.sub.3 [01168]embedded image 1093 CF.sub.2CF.sub.3 [01169]embedded image 1094 CF.sub.2CF.sub.3 [01170]embedded image 1095 CF.sub.2CF.sub.3 [01171]embedded image 1096 CF.sub.2CF.sub.3 [01172]embedded image 1097 CF.sub.2CF.sub.3 [01173]embedded image 1098 CF.sub.3 [01174]embedded image 1099 CF.sub.3 [01175]embedded image 1100 CF.sub.3 [01176]embedded image 1101 CF.sub.3 [01177]embedded image 1102 CF.sub.3 [01178]embedded image 1103 CF.sub.3 [01179]embedded image 1104 CF.sub.3 [01180]embedded image 1105 CF.sub.3 [01181]embedded image 1106 CF.sub.3 [01182]embedded image 1107 CF.sub.3 [01183]embedded image 1108 CF.sub.3 [01184]embedded image 1109 CF.sub.3 [01185]embedded image 1110 CF.sub.3 [01186]embedded image 1111 CF.sub.3 [01187]embedded image 1112 CF.sub.3 [01188]embedded image 1113 CF.sub.3 [01189]embedded image 1114 CF.sub.3 [01190]embedded image 1115 CF.sub.3 [01191]embedded image 1116 CF.sub.3 [01192]embedded image 1117 CF.sub.3 [01193]embedded image 1118 CF.sub.3 [01194]embedded image 1119 CF.sub.3 [01195]embedded image 1120 CF.sub.3 [01196]embedded image 1121 CF.sub.3 [01197]embedded image 1122 CF.sub.3 [01198]embedded image 1123 CF.sub.3 [01199]embedded image 1124 CF.sub.3 [01200]embedded image 1125 CF.sub.3 [01201]embedded image 1126 CF.sub.3 [01202]embedded image 1127 CF.sub.3 [01203]embedded image 1128 CF.sub.3 [01204]embedded image 1129 CF.sub.3 [01205]embedded image 1130 CF.sub.3 [01206]embedded image 1131 CF.sub.3 [01207]embedded image 1132 CF.sub.3 [01208]embedded image 1133 CF.sub.3 [01209]embedded image 1134 CF.sub.3 [01210]embedded image 1135 CF.sub.3 [01211]embedded image 1136 CF.sub.3 [01212]embedded image 1137 CF.sub.3 [01213]embedded image 1138 CF.sub.3 [01214]embedded image 1139 CF.sub.3 [01215]embedded image 1140 CF.sub.3 [01216]embedded image 1141 CF.sub.3 [01217]embedded image 1142 CF.sub.3 [01218]embedded image 1143 CF.sub.3 [01219]embedded image 1144 CF.sub.3 [01220]embedded image 1145 CF.sub.3 [01221]embedded image 1146 CF.sub.3 [01222]embedded image 1147 CF.sub.3 [01223]embedded image 1148 CF.sub.3 [01224]embedded image 1149 CF.sub.3 [01225]embedded image 1150 CF.sub.3 [01226]embedded image 1151 CF.sub.3 [01227]embedded image 1152 CF.sub.3 [01228]embedded image 1153 CF.sub.3 [01229]embedded image 1154 CF.sub.3 [01230]embedded image 1155 CF.sub.3 [01231]embedded image 1156 CF.sub.3 [01232]embedded image 1157 CF.sub.3 [01233]embedded image 1158 CF.sub.3 [01234]embedded image 1159 CF.sub.3 [01235]embedded image 1160 CF.sub.3 [01236]embedded image 1161 CF.sub.3 [01237]embedded image 1162 CF.sub.3 [01238]embedded image 1163 CF.sub.3 [01239]embedded image 1164 CF.sub.3 [01240]embedded image 1165 CF.sub.3 [01241]embedded image 1166 CF.sub.3 [01242]embedded image 1167 CF.sub.3 [01243]embedded image 1168 CF.sub.3 [01244]embedded image 1169 CF.sub.3 [01245]embedded image 1170 CF.sub.3 [01246]embedded image 1171 CF.sub.3 [01247]embedded image 1172 CF.sub.3 [01248]embedded image 1173 CF.sub.3 [01249]embedded image 1174 CF.sub.3 [01250]embedded image 1175 CF.sub.3 [01251]embedded image 1176 CF.sub.3 [01252]embedded image 1177 CF.sub.3 [01253]embedded image 1178 CF.sub.3 [01254]embedded image 1179 CF.sub.3 [01255]embedded image 1180 CF.sub.3 [01256]embedded image 1181 CF.sub.3 [01257]embedded image 1182 CF.sub.3 [01258]embedded image 1183 CF.sub.3 [01259]embedded image 1184 CF.sub.3 [01260]embedded image 1185 CF.sub.3 [01261]embedded image 1186 CF.sub.3 [01262]embedded image 1187 CF.sub.3 [01263]embedded image 1188 CF.sub.3 [01264]embedded image 1189 CF.sub.3 [01265]embedded image 1190 CF.sub.3 [01266]embedded image 1191 CF.sub.3 [01267]embedded image 1192 CF.sub.3 [01268]embedded image 1193 CF.sub.3 [01269]embedded image 1194 CF.sub.3 [01270]embedded image 1195 CF.sub.3 [01271]embedded image 1196 CF.sub.3 [01272]embedded image 1197 CF.sub.3 [01273]embedded image 1198 CF.sub.3 [01274]embedded image 1199 CF.sub.3 [01275]embedded image 1200 CF.sub.3 [01276]embedded image 1201 CF.sub.3 [01277]embedded image 1202 CF.sub.3 [01278]embedded image 1203 CF.sub.3 [01279]embedded image 1204 CF.sub.3 [01280]embedded image 1205 CF.sub.3 [01281]embedded image 1206 CF.sub.3 [01282]embedded image 1207 CF.sub.3 [01283]embedded image 1208 CF.sub.3 [01284]embedded image 1209 CF.sub.3 [01285]embedded image 1210 CF.sub.3 [01286]embedded image 1211 CF.sub.3 [01287]embedded image 1212 CF.sub.3 [01288]embedded image 1213 CF.sub.3 [01289]embedded image 1214 CF.sub.3 [01290]embedded image 1215 CF.sub.3 [01291]embedded image 1216 CF.sub.3 [01292]embedded image 1217 CF.sub.3 [01293]embedded image 1218 CF.sub.3 [01294]embedded image 1219 CF.sub.3 [01295]embedded image 1220 CF.sub.3 [01296]embedded image 1221 CF.sub.3 [01297]embedded image 1222 CF.sub.3 [01298]embedded image 1223 CF.sub.3 [01299]embedded image 1224 CF.sub.3 [01300]embedded image 1225 CF.sub.3 [01301]embedded image 1226 CF.sub.3 [01302]embedded image 1227 CF.sub.3 [01303]embedded image 1228 CF.sub.3 [01304]embedded image 1229 CF.sub.3 [01305]embedded image 1030 CF.sub.3 [01306]embedded image 1231 CF.sub.3 [01307]embedded image 1232 CF.sub.3 [01308]embedded image 1233 CF.sub.3 [01309]embedded image 1234 CF.sub.3 [01310]embedded image 1235 CF.sub.3 [01311]embedded image 1236 CF.sub.3 [01312]embedded image 1237 CF.sub.3 [01313]embedded image 1238 CF.sub.3 [01314]embedded image 1239 CF.sub.3 [01315]embedded image 1240 CF.sub.3 [01316]embedded image 1241 CF.sub.3 [01317]embedded image 1242 CF.sub.3 [01318]embedded image 1243 CF.sub.3 [01319]embedded image 1244 CF.sub.3 [01320]embedded image 1245 CF.sub.3 [01321]embedded image 1246 CF.sub.3 [01322]embedded image 1247 CF.sub.3 [01323]embedded image 1248 CF.sub.3 [01324]embedded image 1249 CF.sub.3 [01325]embedded image 1250 CF.sub.3 [01326]embedded image 1251 CF.sub.3 [01327]embedded image 1252 CF.sub.3 [01328]embedded image 1253 CF.sub.3 [01329]embedded image 1254 CF.sub.3 [01330]embedded image 1255 CF.sub.3 [01331]embedded image 1256 CF.sub.3 [01332]embedded image 1257 CF.sub.3 [01333]embedded image 1258 CF.sub.3 [01334]embedded image 1259 CF.sub.3 [01335]embedded image 1260 CF.sub.3 [01336]embedded image 1261 CF.sub.3 [01337]embedded image 1262 CF.sub.3 [01338]embedded image 1263 CF.sub.3 [01339]embedded image 1264 CF.sub.3 [01340]embedded image 1265 CF.sub.3 [01341]embedded image 1266 CF.sub.3 [01342]embedded image 1267 CF.sub.3 [01343]embedded image 1268 CF.sub.3 [01344]embedded image 1269 CF.sub.3 [01345]embedded image 1270 CF.sub.3 [01346]embedded image 1271 CF.sub.3 [01347]embedded image 1272 CF.sub.3 [01348]embedded image 1273 CF.sub.3 [01349]embedded image 1274 CF.sub.3 [01350]embedded image 1275 CF.sub.3 [01351]embedded image 1276 CF.sub.3 [01352]embedded image 1277 CF.sub.3 [01353]embedded image 1278 CF.sub.3 [01354]embedded image 1279 CF.sub.3 [01355]embedded image 1280 CF.sub.3 [01356]embedded image 1281 CF.sub.3 [01357]embedded image 1282 CF.sub.3 [01358]embedded image 1283 CF.sub.3 [01359]embedded image 1284 CF.sub.3 [01360]embedded image 1285 CF.sub.3 [01361]embedded image 1286 CF.sub.3 [01362]embedded image .sup.1H NMR (500 MHz, Chloroform-d) 7.25 (d, J = 2.0 Hz, 1H), 7.19 (dd, J = 7.5, 2.0 Hz, 1H), 7.06-6.91 (m, 2H), 5.52 (s, 1H). 1287 CF.sub.3 [01363]embedded image .sup.1H NMR (500 MHz, Chloroform-d) 7.83 (d, J = 7.5 Hz, 2H), 7.59 (d, J = 7.5 Hz, 2H), 7.10 (s, 1H), 5.88 (s, 1H), 0.25 (s, 9H). 1288 CF.sub.3 [01364]embedded image 1289 CF.sub.3 [01365]embedded image 1290 CF.sub.3 [01366]embedded image 1291 CF.sub.3 [01367]embedded image 1292 CF.sub.3 [01368]embedded image 1293 CF.sub.3 [01369]embedded image 1294 CF.sub.3 [01370]embedded image 1295 CF.sub.3 [01371]embedded image 1296 CF.sub.3 [01372]embedded image 1297 CF.sub.3 [01373]embedded image 1298 CF.sub.3 [01374]embedded image 1299 CF.sub.3 [01375]embedded image 1300 CF.sub.3 [01376]embedded image 1301 CF.sub.3 [01377]embedded image 1302 CF.sub.3 [01378]embedded image 1303 CF.sub.3 [01379]embedded image 1304 CF.sub.3 [01380]embedded image 1305 CF.sub.3 [01381]embedded image 1306 CF.sub.3 [01382]embedded image 1307 CF.sub.3 [01383]embedded image 1308 CF.sub.3 [01384]embedded image 1309 CF.sub.3 [01385]embedded image 1310 CF.sub.3 [01386]embedded image 1311 CF.sub.3 [01387]embedded image 1312 CF.sub.3 [01388]embedded image 1313 CF.sub.3 [01389]embedded image 1314 CF.sub.3 [01390]embedded image 1315 CF.sub.3 [01391]embedded image 1316 CF.sub.3 [01392]embedded image 1317 CF.sub.3 [01393]embedded image 1318 CF.sub.3 [01394]embedded image 1319 CF.sub.3 [01395]embedded image 1320 CF.sub.3 [01396]embedded image 1321 CF.sub.3 [01397]embedded image 1322 CF.sub.3 [01398]embedded image 1323 CF.sub.3 [01399]embedded image 1324 CF.sub.3 [01400]embedded image 1325 CF.sub.3 [01401]embedded image 1326 CF.sub.3 [01402]embedded image 1327 CF.sub.3 [01403]embedded image 1328 CF.sub.3 [01404]embedded image 1329 CF.sub.3 [01405]embedded image 1330 CF.sub.3 [01406]embedded image 1331 CF.sub.3 [01407]embedded image 1332 CF.sub.3 [01408]embedded image 1333 CF.sub.3 [01409]embedded image 1334 CF.sub.3 [01410]embedded image 1335 CF.sub.3 [01411]embedded image 1336 CF.sub.3 [01412]embedded image 1337 CF.sub.3 [01413]embedded image 1338 CF.sub.3 [01414]embedded image 1339 CF.sub.3 [01415]embedded image 1340 CF.sub.3 [01416]embedded image 1341 CF.sub.3 [01417]embedded image 1342 CF.sub.3 [01418]embedded image 1343 CF.sub.3 [01419]embedded image 1344 CF.sub.3 [01420]embedded image 1345 CF.sub.3 [01421]embedded image 1346 CF.sub.3 [01422]embedded image 1347 CF.sub.3 [01423]embedded image 1348 CF.sub.3 [01424]embedded image 1349 CF.sub.3 [01425]embedded image 1350 CF.sub.3 [01426]embedded image 1351 CF.sub.3 [01427]embedded image 1352 CF.sub.3 [01428]embedded image 1353 CF.sub.3 [01429]embedded image 1354 CF.sub.3 [01430]embedded image 1355 CF.sub.3 [01431]embedded image 1356 CF.sub.3 [01432]embedded image 1357 CF.sub.3 [01433]embedded image 1358 CF.sub.3 [01434]embedded image 1359 CF.sub.3 [01435]embedded image 1360 CF.sub.3 [01436]embedded image 1361 CF.sub.3 [01437]embedded image 1362 CF.sub.3 [01438]embedded image 1363 CF.sub.3 [01439]embedded image 1364 CF.sub.3 [01440]embedded image 1365 CF.sub.3 [01441]embedded image 1366 CF.sub.3 [01442]embedded image 1367 CF.sub.3 [01443]embedded image 1368 CF.sub.3 [01444]embedded image 1369 CF.sub.3 [01445]embedded image 1370 CF.sub.3 [01446]embedded image 1371 CF.sub.3 [01447]embedded image 1372 CF.sub.3 [01448]embedded image 1373 CF.sub.3 [01449]embedded image 1374 CF.sub.3 [01450]embedded image 1375 CF.sub.3 [01451]embedded image 1376 CF.sub.3 [01452]embedded image 1377 CF.sub.3 [01453]embedded image 1378 CF.sub.3 [01454]embedded image 1379 CF.sub.3 [01455]embedded image 1380 CF.sub.3 [01456]embedded image 1381 CF.sub.3 [01457]embedded image 1382 CF.sub.3 [01458]embedded image 1383 CF.sub.3 [01459]embedded image 1384 CF.sub.3 [01460]embedded image 1385 CF.sub.3 [01461]embedded image 1386 CF.sub.3 [01462]embedded image 1387 CF.sub.3 [01463]embedded image 1388 CF.sub.3 [01464]embedded image 1389 CF.sub.3 [01465]embedded image 1390 CF.sub.3 [01466]embedded image 1391 CF.sub.3 [01467]embedded image 1392 CF.sub.3 [01468]embedded image 1393 CF.sub.3 [01469]embedded image 1394 CF.sub.3 [01470]embedded image 1395 CF.sub.3 [01471]embedded image 1396 CF.sub.3 [01472]embedded image 1397 CF.sub.3 [01473]embedded image 1398 CF.sub.3 [01474]embedded image 1399 CF.sub.3 [01475]embedded image 1400 CF.sub.3 [01476]embedded image 1401 CF.sub.3 [01477]embedded image 1402 CF.sub.3 [01478]embedded image 1403 CF.sub.3 [01479]embedded image 1404 CF.sub.3 [01480]embedded image 1405 CF.sub.3 [01481]embedded image 1406 CF.sub.3 [01482]embedded image 1407 CF.sub.3 [01483]embedded image 1408 CF.sub.3 [01484]embedded image 1409 CF.sub.3 [01485]embedded image 1410 CF.sub.3 [01486]embedded image 1411 CF.sub.3 [01487]embedded image 1412 CF.sub.3 [01488]embedded image 1413 CF.sub.3 [01489]embedded image 1414 CF.sub.3 [01490]embedded image 1415 CF.sub.3 [01491]embedded image 1416 CF.sub.3 [01492]embedded image 1417 CF.sub.3 [01493]embedded image 1418 CF.sub.3 [01494]embedded image 1419 CF.sub.3 [01495]embedded image 1420 CF.sub.3 [01496]embedded image 1421 CF.sub.3 [01497]embedded image 1422 CF.sub.3 [01498]embedded image 1423 CF.sub.3 [01499]embedded image 1424 CF.sub.3 [01500]embedded image 1425 CF.sub.3 [01501]embedded image 1426 CF.sub.3 [01502]embedded image 1427 CF.sub.3 [01503]embedded image 1428 CF.sub.3 [01504]embedded image 1429 CF.sub.3 [01505]embedded image 1430 CF.sub.3 [01506]embedded image 1431 CF.sub.3 [01507]embedded image 1432 CF.sub.3 [01508]embedded image 1433 CF.sub.3 [01509]embedded image 1434 CF.sub.3 [01510]embedded image 1435 CF.sub.3 [01511]embedded image 1436 CF.sub.3 [01512]embedded image 1437 CF.sub.3 [01513]embedded image 1438 CF.sub.3 [01514]embedded image 1439 CF.sub.3 [01515]embedded image 1440 CF.sub.3 [01516]embedded image 1441 CF.sub.3 [01517]embedded image 1442 CF.sub.3 [01518]embedded image 1443 CF.sub.3 [01519]embedded image 1444 CF.sub.3 [01520]embedded image 1445 CF.sub.3 [01521]embedded image 1446 CF.sub.3 [01522]embedded image 1447 CF.sub.3 [01523]embedded image 1448 CF.sub.3 [01524]embedded image 1449 CF.sub.3 [01525]embedded image 1450 CF.sub.3 [01526]embedded image 1451 CF.sub.3 [01527]embedded image 1452 CF.sub.3 [01528]embedded image 1453 CF.sub.3 [01529]embedded image 1454 CF.sub.3 [01530]embedded image 1455 CF.sub.3 [01531]embedded image 1456 CF.sub.3 [01532]embedded image 1457 CF.sub.3 [01533]embedded image 1458 CF.sub.3 [01534]embedded image 1459 CF.sub.3 [01535]embedded image 1460 CF.sub.3 [01536]embedded image 1461 CF.sub.3 [01537]embedded image 1462 CF.sub.3 [01538]embedded image 1463 CF.sub.3 [01539]embedded image 1464 CF.sub.3 [01540]embedded image 1465 CF.sub.3 [01541]embedded image 1466 CF.sub.3 [01542]embedded image 1467 CF.sub.3 [01543]embedded image 1468 CF.sub.3 [01544]embedded image 1469 CF.sub.3 [01545]embedded image 1470 CF.sub.2CF.sub.3 [01546]embedded image 1471 CH.sub.2F [01547]embedded image 1472 CHF.sub.2 [01548]embedded image 1473 CF.sub.2CF.sub.3 [01549]embedded image 1474 CHF.sub.2 [01550]embedded image 1475 CHF.sub.2 [01551]embedded image 1476 CF.sub.2CF.sub.3 [01552]embedded image 1477 CH.sub.2F [01553]embedded image 1478 OCHF.sub.2 [01554]embedded image 1479 CF.sub.2CF.sub.3 [01555]embedded image 1480 CF.sub.2CF.sub.3 [01556]embedded image 1481 CF.sub.2CF.sub.3 [01557]embedded image 1482 CF.sub.2CF.sub.3 [01558]embedded image 1483 Ph [01559]embedded image 1484 CF.sub.2CF.sub.3 [01560]embedded image 1485 CF.sub.2CF.sub.3 [01561]embedded image 1486 CF.sub.2CF.sub.3 [01562]embedded image 1487 CN [01563]embedded image 1488 CF.sub.2CF.sub.3 [01564]embedded image 1489 CF.sub.2CF.sub.3 [01565]embedded image 1490 CF.sub.2CF.sub.3 [01566]embedded image 1491 CF.sub.2CF.sub.3 [01567]embedded image 1492 CF.sub.2CF.sub.3 [01568]embedded image 1493 CF.sub.3 [01569]embedded image .sup.1H NMR (500 MHz, Chloroform-d) 7.16 (s, 1H), 5.85 (s, 1H), 4.27 (s, 3H). 1494 CF.sub.3 [01570]embedded image 1495 CF.sub.3 [01571]embedded image 1496 CF.sub.3 [01572]embedded image 1497 CF.sub.3 [01573]embedded image 1498 CF.sub.3 [01574]embedded image 1499 CF.sub.3 [01575]embedded image 1500 CF.sub.3 [01576]embedded image 1501 CF.sub.3 [01577]embedded image 1502 CF.sub.3 [01578]embedded image 1503 CF.sub.3 [01579]embedded image 1504 CF.sub.3 [01580]embedded image 1505 CF.sub.3 [01581]embedded image 1506 CF.sub.3 [01582]embedded image 1507 CONH.sub.2 [01583]embedded image 1508 CF.sub.3 [01584]embedded image 1509 CF.sub.3 [01585]embedded image 1510 CF.sub.3 [01586]embedded image 1511 CF.sub.3 [01587]embedded image 1512 CF.sub.3 [01588]embedded image .sup.1H NMR (500 MHz, Chloroform-d) 7.34 (s, 1H), 7.08 (s, 1H), 7.04 (s, 1H), 5.78 (s, 1H), 5.53 (s, 1H). 1513 Ph [01589]embedded image 1514 CF.sub.3 [01590]embedded image 1515 CF.sub.3 [01591]embedded image 1516 NH.sub.2 [01592]embedded image 1517 CF.sub.3 [01593]embedded image 1518 CF.sub.3 [01594]embedded image 1519 CF.sub.3 [01595]embedded image 1520 CF.sub.3 [01596]embedded image 1521 CF.sub.3 [01597]embedded image 1522 CF.sub.3 [01598]embedded image .sup.1H NMR (500 MHz, Chloroform-d) δ 7.74 (d, J = 15.0 Hz, 1H), 7.00 (s, 1H), 6.50 (d, J = 15.0 Hz, 1H), 5.87 (s, 1H), 4.24 (q, J = 8.0 Hz, 2H), 1.31 (t, J = 8.0 Hz, 3H). 1523 CF.sub.3 [01599]embedded image .sup.1H NMR (500 MHz, Chloroform-d) δ 6.99 (s, 1H), 6.25 (s, 1H), 5.87 (s, 1H), 1.78 (s, 6H). 1524 CF.sub.3 [01600]embedded image .sup.1H NMR (500 MHz, Chloroform-d) δ 7.07 (s, 1H), 6.07-5.96 (m, 1H), 5.87 (s, 1H), 2.03-1.93 (m, 4H), 1.66-1.56 (m, 4H). 1525 CF.sub.3 Me (500 MHz, Chloroform-7) 5 6.96 (s, 1H), 5.87 (s, 1H), 2.10 (s, 3H). 1526 CF.sub.3 [01601]embedded image 1527 OH [01602]embedded image 1528 CF.sub.3 [01603]embedded image (500 MHz, Chloroform-d) δ 6.95 (s, 1H), 6.38-6.31 (m, 1H), 5.87 (s, 1H), 2.35-2.24 (m, 4H), 1.82-1.70 (m, 2H). 1529 CF.sub.3 [01604]embedded image (500 MHz, Chloroform-d) δ 6.99 (s, 1H), 5.87 (s, 1H), 5.65-5.42 (m, 1H), 4.31-4.22 (m, 2H), 2.62-2.54 (m, 2H). 1530 CF.sub.3 [01605]embedded image (500 MHz, Chloroform-d) δ 7.03 (s, 1H), 6.22 (d, J = 15.0 Hz, 1H), 5.93- 5.85 (m, 2H), 0.08 (s, 9H). 1531 CF.sub.3 [01606]embedded image (500 MHz, Chloroform-d) δ 7.09 (s, 1H), 5.87 (s, 1H), 5.81-5.74 (m, 1H), 4.20-4.04 (m, 2H), 3.79-3.66 (m, 2H), 2.13-2.01 (m, 2H). 1532 CF.sub.3 [01607]embedded image (500 MHz, Chloroform-d) δ 7.03 (s, 1H), 6.40-6.26 (m, 2H), 5.87 (s, 1H), 2.07-1.97 (m, 2H), 1.46-1.32 (m, 2H), 0.95 (t, J = 8.0 Hz, 3H). 1533 CF.sub.3 Et (500 MHz, Chloroform-d) δ 6.96 (s, 1H), 5.87 (s, 1H), 2.41 (q, J = 8.0 Hz, 2H), 1.16 (t, J = 8.0 Hz, 3H). 1534 OCF.sub.3 [01608]embedded image 1535 CF.sub.3 [01609]embedded image 1536 CN [01610]embedded image 1537 CF.sub.3 [01611]embedded image 1538 CF.sub.3 [01612]embedded image 1539 CF.sub.3 [01613]embedded image 1540 CF.sub.3 [01614]embedded image 1541 CF.sub.3 [01615]embedded image 1542 CF.sub.3 [01616]embedded image 1543 CF.sub.2CF.sub.3 [01617]embedded image 1544 CF.sub.3 [01618]embedded image 1545 CF.sub.3 [01619]embedded image 1546 CF.sub.3 [01620]embedded image 1547 CHF.sub.2 [01621]embedded image 1548 CF.sub.3 [01622]embedded image 1549 CF.sub.3 [01623]embedded image [01624]text missing or illegible when filed

    TABLE-US-00002 TABLE 2 Structure and .sup.1HNMR data of the derivative Compound 1-1 I-1 [01625]embedded image No. X M A .sup.1HNMR 1-1 CF.sub.3 [01626]embedded image [01627]embedded image (500 MHz, Chloroform-d) δ 7.43-7.27 (m, 3H), 7.15- 7.02 (m, 2H), 2.47 (s, 3H). 1-2 CF.sub.3 [01628]embedded image [01629]embedded image (500 MHz, Chloroform-d) δ 7.47-7.39 (m, 2H), 7.18 (s, 1H), 7.11-7.03 (m, 2H), 2.47 (s, 3H). 1-3 CF.sub.3 [01630]embedded image [01631]embedded image (500 MHz, Chloroform-d) δ 7.45-7.33 (m, 2H), 7.20- 7.11 (m, 2H), 2.27 (q, 7 = 8.0 Hz, 1H), 1.12 (t, J = 8.0 Hz, 2H). 1-4 CF.sub.3 [01632]embedded image [01633]embedded image (500 MHz, Chloroform-d) δ 7.45-7.37 (m, 2H), 7.18 (s, 1H), 7.11-7.03 (m, 2H), 2.27 (q, J = 8.0 Hz, 2H), 1.03 (t, J = 8.0 Hz, 3H). 1-5 CF.sub.3 [01634]embedded image [01635]embedded image (500 MHz, Chloroform-d) δ 7.37-7.31 (m,2H),7.17(s, 1H), 6.84-6.78 (m, 2H), 2.78 (t, J = 8.0 Hz, 2H), 2.27 (s, 3H), 1.73- 1.62 (m, 2H), 1.38 (t, J = 8.0 Hz, 3H). 1-6 CF.sub.3 [01636]embedded image [01637]embedded image (500 MHz, Chloroform-d) δ 7.43-7.36 (m, 2H), 7.17 (s, 1H), 6.80-6.74 (m, 2H), 3.80 (s, 3H), 2.70 (hept, J = 6.5 Hz, 1H), 1.17 (d, J = 6.5 Hz, 6H). 1-7 CF.sub.3 [01638]embedded image [01639]embedded image (500 MHz, Chloroform-d) δ 7.63 (d, J = 2.0 Hz, 1H), 7.31 (dd, J = 7.5, 2.0 Hz, 1H), 7.26 (d, J = 7.5 Hz, 1H), 7.18 (s, 1H), 2.33 (t, J = 8.0 Hz, 2H), 1.53-1.41 (m, 4H), 0.92 (t, J = 8.0 Hz, 3H). 1-8 CF.sub.3 [01640]embedded image [01641]embedded image (500 MHz, Chloroform-d) δ 7.98-7.89 (m, 2H), 7.75- 7.63 (m, 2H),7.19(s, 1H), 4.08 (d, J = 7.0 Hz, 2H), 2.19- 2.02 (m, 1H), 0.97 (d,7 = 7.0 Hz, 6H). 1-9 CF.sub.3 [01642]embedded image [01643]embedded image (500 MHz, Chloroform-d) δ 9.13 (d, J = 1.5 Hz, 1H), 8.09 (dd, J = 8.0,1.5 Hz, 1H), 7.41 (d, J = 7.0 Hz, 2H), 1.16 (s, 9H). 1-10 CF.sub.3 [01644]embedded image [01645]embedded image (500 MHz, Chloroform-d) δ 7.92 (d, J = 7.5 Hz, 2H), 7.70 (d,7 = 7.5 Hz, 2H),7.18 (s, 1H), 2.33 (t, J = 8.0 Hz, 2H), 1.50-1.23 (m, 6H), 0.92 (t, J = 8.0 Hz, 3H). 1-11 CF.sub.3 [01646]embedded image [01647]embedded image (500 MHz, Chloroform-d) δ 7.96-7.90 (m, 2H), 7.90- 7.84 (m, 2H), 7.26 (s, 1H), 3.30 (s, 3H), 2.09 (s, 2H), 0.93 (s, 9H). 1-12 CF.sub.3 [01648]embedded image [01649]embedded image (500 MHz, Chloroform-d) δ 8.41-8.21 (m, 2H), 7.91- 7.60 (m, 2H),7.19(s, 1H), 2.14-1.77 (m, 3H), 1.75- 1.53 (m, 2H), 1.45-1.24 (m, 4H), 0.90 (t, J = 7.5 Hz, 3H), 0.79 (t, J = 8.0 Hz, 3H). 1-13 CF.sub.3 [01650]embedded image [01651]embedded image (500 MHz, Chloroform-d) δ 7.18-7.08 (m, 2H), 6.93- 6.68 (m, 2H), 6.62-6.47 (m, 1H), 4.13(s, 2H), 2.33 (t, J = 6.0 Hz, 2H), 1.51-1.22 (m, 8H), 0.93 (t, J = 8.0 Hz, 3H). 1-14 CF.sub.3 [01652]embedded image [01653]embedded image (500 MHz, Chloroform-d) δ 7.41-7.19 (m, 2H), 7.23- 7.10 (m, 2H), 2.33 (t, J = 8.0 Hz, 2H), 1.51-1.36 (m, 2H), 1.34-1.22 (m, 8H), 0.94 (t, J = 8.0 Hz, 3H). 1-15 CF.sub.3 [01654]embedded image [01655]embedded image (500 MHz, Chloroform-d) δ 7.62-7.52 (m, 2H), 7.46- 7.29 (m, 2H),7.14(s, 1H), 2.33 (t, J = 8.0 Hz, 2H), 1.51- 1.22 (m, 12H), 0.93 (t, J = 8.0 Hz, 3H). 1-16 CF.sub.3 [01656]embedded image [01657]embedded image (500 MHz, Chloroform-d) δ 7.47-7.39 (m, 2H), 7.11- 7.03 (m, 2H), 2.33 (t, J = 7.5 Hz, 2H), 1.51-1.22 (m, 22H), 0.89 (t, J = 8.0 Hz, 3H). 1-17 CF.sub.3 [01658]embedded image [01659]embedded image (500 MHz, Chloroform-d) δ 7.59-7.52 (m, 2H), 7.41- 7.31 (m, 3H), 2.33 (t, J = 7.5 Hz, 2H), 1.51-1.22 (m, 30H), 0.87 (t, J = 8.0 Hz, 3H). 1-18 CF.sub.3 [01660]embedded image [01661]embedded image (500 MHz, Chloroform-d) δ 7.70 (d, J = 7.5 Hz, 2H), 7.43 (d, J = 7.5 Hz, 2H), 7.13 (s, 1H), 4.08 (d, J = 7.0 Hz, 2H), 1.71-1.52 (m, 7H), 1.28- 1.17 (m, 2H). 1-19 CF.sub.3 [01662]embedded image [01663]embedded image (500 MHz, Chloroform-d) δ 7.53-7.45 (m, 2H), 7.46- 7.37 (m, 3H), 7.18 (s, 1H), 2.37-2.29 (m, 1H), 2.25- 2.14 (m, 2H), 1.82-1.63 (m, 5H), 1.53-1.40 (m,3H). 1-20 CF.sub.3 [01664]embedded image [01665]embedded image (500 MHz, Chloroform-d) δ 7.47-7.27 (m, 2H), 7.22- 7.14 (m, 1H), 7.17-7.00 (m, 2H), 5.54-5.42 (m, 1H), 1.87 -1.72(m, 3H). 1-21 CF.sub.3 [01666]embedded image [01667]embedded image (500 MHz, Chloroform-d) δ 7.39-7.32 (m, 2H), 7.32- 7.26 (m, 2H),7.14 (s, 1H), 2.75 (q, J = 8.0 Hz, 2H), 2.71- 2.61 (m, 2H), 1.21 (t, J = 8.0 Hz, 3H). 1-22 CF.sub.3 [01668]embedded image [01669]embedded image (500 MHz, Chloroform-d) δ 7.72-7.67 (m, 2H), 7.59- 7.52 (m, 2H),7.17 (s, 1H), 4.49 (q, J = 6.5 Hz, 1H), 1.72 (d, J = 6.5 Hz, 3H). 1-23 CF.sub.3 [01670]embedded image [01671]embedded image (500 MHz, Chloroform-d) δ 7.44-7.30 (m, 2H), 7.25- 7.17 (m, 2H), 3.28(t, J = 7.0 Hz, 2H), 2.33 (t, J = 7.5 Hz, 2H), 2.06-1.98 (m, 2H). 1-24 CF.sub.3 [01672]embedded image [01673]embedded image 1-25 CF.sub.3 [01674]embedded image [01675]embedded image (500 MHz, Chloroform-d) δ 7.48-7.40 (m, 2H), 7.24 (s, 1H), 7.11-7.03 (m, 2H). 1-26 CF.sub.3 [01676]embedded image [01677]embedded image (500 MHz, Chloroform-d) δ 7.43-7.22 (m, 2H), 7.20- 7.11 (m,2H), 4.25 (q, J = 8.0 Hz, 2H), 1.26 (t, J = 8.0 Hz, 3H). 1-27 CF.sub.3 [01678]embedded image [01679]embedded image (500 MHz, Chloroform-d) δ 7.51-7.45 (m, 2H), 7.09- 7.03 (m, 2H), 4.23 (t, J = 7.5 Hz, 2H), 4.00 (t, J = 7.5 Hz, 2H), 1.87-1.50 (m, 6H), 1.02 (t, J = 8.0 Hz, 3H), 0.92 (t, J = 8.0 Hz, 3H). 1-28 CF.sub.3 [01680]embedded image [01681]embedded image (500 MHz, Chloroform-d) δ 7.50(d, J = 7.5Hz, 2H), 7.21 (s, 1H), 7.10 (d, J = 7.5 Hz, 2H), 5.15 (hept, J = 6.5 Hz, 1H), 2.77 (q, J = 7.5 Hz, 2H), 1.26-1.15 (m, 9H). 1-29 CF.sub.3 [01682]embedded image [01683]embedded image (500 MHz, Chloroform-d) δ 7.48-7.40 (m, 2H), 7.21 (s, 1H), 7.11-7.03 (m, 2H), 4.23 (t, J = 7.5 Hz, 2H), 1.60-1.40 (m, 4H), 0.98 (t, J = 8.0 Hz, 3H). 1-30 CF.sub.3 [01684]embedded image [01685]embedded image (500 MHz, Chloroform-d) δ 7.99-7.90 (m, 2H), 7.75- 7.69-7.61 (m, 2H), 7.22 (s, 1H), 4.05 (d, J = 7.0 Hz, 2H), 1.95- 1.80 (m, 1H), 0.95 (d, J = 6.5 Hz, 6H). 1-31 CF.sub.3 [01686]embedded image [01687]embedded image (500 MHz, Chloroform-d) δ 7.43-7.22 (m, 2H), 7.21- 7.11 (m, 2H), 4.23 (t, J = 7.5 Hz, 2H), 1.79-1.39 (m, 6H), 0.95 (t, J = 8.0 Hz, 3H). 1-32 CF.sub.3 [01688]embedded image [01689]embedded image (500 MHz, Chloroform-d) δ 7.36-7.28 (m, 2H), 7.20 (s, 1H), 7.13 (dd, J = 7.5, 1.0 Hz, 1H), 4.23 (t, J = 7.5 Hz, 2H), 2.30 (s, 3H), 2.20 (s, 3H), 1.78 -1.52 (m, 3H), 0.97 (d, J = 7.0 Hz, 6H). 1-33 CF.sub.3 [01690]embedded image [01691]embedded image (500 MHz, Chloroform-d) δ 7.96 (d, J = 2.5 Hz, 1H), 7.83 (dd, J = 7.5, 2.5 Hz, 1H), 7.48 (d, J = 7.5 Hz, 1H),7.22(s, 1H), 4.02 (s, 2H), 2.50 (s, 3H), 0.95 (s, 9H). 1-34 CF.sub.3 [01692]embedded image [01693]embedded image (500 MHz, Chloroform-d) δ 8.77 (d, J = 2.0 Hz, 1H), 8.57 (dd, J = 7.5, 2.0 Hz, 1H), 8.25 (d, J = 7.5 Hz, 1H),7.24(s, 1H), 1.61 (s, 6H), 1.49 (q, J = 8.0 Hz, 2H), 0.90 (t, J = 8.0 Hz, 3H). 1-35 CF.sub.3 [01694]embedded image [01695]embedded image (500 MHz, Chloroform-d) δ 8.05 (d, J = 2.0 Hz, 1H),7.80- 7.70 (m, 2H), 7.22 (s, 1H), 4.23 (t, J = 7.5 Hz, 2H), 1.72- 1.31 (m, 8H), 0.93 (t, J = 7.5 Hz, 3H). 1-36 CF.sub.3 [01696]embedded image [01697]embedded image (500 MHz, Chloroform-d) δ 8.08 (d, J = 2.0 Hz, 1H), 7.93 (dd, J = 7.5, 2.0 Hz, 1H), 7.82 (d, J = 7.5 Hz, 1H), 7.20 (s, 1H), 4.79-4.53 (m, 1H), 2.06 -1.88 (m, 2H), 1.71-1.57 (m, 4H), 1.30-1.19 (m, 2H), 0.89 (t, J = 8.0 Hz, 3H), 0.78 (t, J = 8.0 Hz, 3H). 1-37 CF.sub.3 [01698]embedded image [01699]embedded image (500 MHz, Chloroform-d) δ 8.04 (d, J = 2.0 Hz, 1H), 7.82 (dd, 7 = 7.5, 2.0 Hz, 1H), 7.20 (s, 1H), 7.15 (d, J = 7.5 Hz, 1H), 4.27-4.19 (m, 2H), 4.04 (s, 3H), 1.85- 1.75 (m, 2H), 1.79-1.71 (m, 1H), 1.65- 1.51 (m, 2H), 1.40-1.20 (m, 2H), 1.18-1.05 (m,2H), 0.89 (t, J = 8.0 Hz, 3H), 0.83 (t, J = 8.0 Hz, 3H). 1-38 CF.sub.3 [01700]embedded image [01701]embedded image (500 MHz, Chloroform-d) δ 7.38 (d, J = 7.5 Hz, 1H), 7.23- 7.16 (m,2H), 4.23 (t, J = 7.5 Hz, 2H), 1.72-1.61 (m, 2H), 1.47- 1.28 (m, 8H), 0.93 (t, J = 8.0 Hz, 3H). 1-39 CF.sub.3 [01702]embedded image [01703]embedded image (500 MHz, Chloroform-d) δ 7.41-7.34 (m, 2H), 7.21- 7.03 (m, 3H), 4.23 (t, J = 7.5 Hz, 2H), 1.72-1.35 (m, 12H), 0.93 (t, J = 8.0 Hz, 3H). 1-40 CF.sub.3 [01704]embedded image [01705]embedded image (500 MHz, Chloroform-d) δ 7.69 (d, J = 7.5 Hz, 2H), 7.57- 7.31 (d, J = 7.5 Hz, 2H), 7.10 (s, 1H), 4.23 (t, J = 7.5 Hz, 1H), 1.72-1.35 (m, 12H), 0.93 (t, J = 8.0 Hz, 3H). 1-41 CF.sub.3 [01706]embedded image [01707]embedded image (500 MHz, Chloroform-d) δ 7.49 (d, J = 7.5 Hz, 2H), 7.09 (d, J = 7.5 Hz, 2H), 7.02 (s, 1H), 4.23 (t, J = 7.5 Hz, 1H), 4.00 (t, J = 7.5 Hz, 1H), 1.73- 1.49 (m, 4H), 1.35-1.04 (m, 16H), 0.93-0.85 (m, 6H). 1-42 CF.sub.3 [01708]embedded image [01709]embedded image (500 MHz, Chloroform-d) δ 7.47-7.35 (m, 2H), 7.23- 7.11 (m, 2H), 2.91 (q, J = 7.0 Hz, 2H), 1.26 (t, J = 7.0 Hz, 3H). 1-43 CF.sub.3 [01710]embedded image [01711]embedded image (500 MHz, Chloroform-d) δ 7.48-7.40 (m, 2H), 7.21 (s, 1H), 7.11-7.03 (m, 2H), 2.85 (t, J = 8.0 Hz, 2H), 1.66-1.50 (m, 2H), 0.90 (t, J = 8.0 Hz, 3H). 1-44 CF.sub.3 [01712]embedded image [01713]embedded image (500 MHz, Chloroform-d) δ 7.57-7.51 (m, 2H), 7.38- 7.30 (m, 3H), 7.17-7.08 (m, 3H), 7.02-6.96 (m, 2H), 3.29 (hept, J = 6.5 Hz, 1H), 1.46 (d, J = 6.5 Hz, 6H). 1-45 CF.sub.3 [01714]embedded image [01715]embedded image (500 MHz, Chloroform-d) δ 7.49 (d, J = 7.5 Hz, 2H), 7.38 (d, J = 7.5 Hz, 2H), 7.33 (s, 1H), 2.85 (t, J = 8.0 Hz, 2H), 2.55-2.42 (m, 1H), 2.15- 2.07 (m, 2H), 1.82-1.70 (m, 6H), 1.43- 1.38 (m, 4H), 1.37 -1.26(m, 2H), 0.87 (t, J = 8.0 Hz, 3H). 1-46 CF.sub.3 [01716]embedded image [01717]embedded image (500 MHz, Chloroform-d) δ 7.31 (s, 1H), 7.13-6.97 (m, 2H), 6.76-6.67 (m, 2H), 4.13 (s, 2H), 3.26-3.18 (m, 1H), 1.73-1.60 (m, 2H), 1.36 (d, J = 6.5 Hz, 3H), 0.90 (t, J = 8.0 Hz, 3H). 1-47 CF.sub.3 [01718]embedded image [01719]embedded image (500 MHz, Chloroform-d) δ 7.52-7.43 (m, 3H), 7.29 (s, 1H), 1.26 (s, 9H). 1-48 CF.sub.3 [01720]embedded image [01721]embedded image (500 MHz, Chloroform-d) δ 7.52 (d, J = 2.0 Hz, 1H), 7.45 (d, J = 7.5 Hz, 1H), 7.35-7.27 (m, 2H), 2.85 (t, J = 7.5 Hz, 2H), 1.56- 1.23 (m, 6H), 0.94 (t, J = 8.0 Hz, 3H). 1-49 CF.sub.3 [01722]embedded image [01723]embedded image (500 MHz, Chloroform-d) δ 7.42-7.37 (m, 1H), 7.23- 7.14 (m, 3H), 2.85 (t, J = 8.0 Hz, 2H), 2.50 (s, 3H), 2.40 (s, 3H), 1.68-1.47 (m,3H), 0.88 (d, J = 6.5 Hz, 6H). 1-50 CF.sub.3 [01724]embedded image [01725]embedded image (500 MHz, Chloroform-d) δ 7.55 (d, J = 7.5 Hz, 2H), 7.41 (d, J = 7.5 Hz, 2H), 7.17 (s, 1H), 2.45 (s, 3H), 1.88 (q, J = 8.0 Hz, 1H), 1.24 (s, 6H), 0.85 (t, J = 8.0 Hz, 3H). 1-51 CF.sub.3 [01726]embedded image [01727]embedded image (500 MHz, Chloroform-d) δ 7.81-7.61 (m, 1H), 7.49- 7.28 (m, 2H), 7.22 (s, 1H), 2.73 (s, 2H), 0.95 (s, 9H). 1-52 CF.sub.3 [01728]embedded image [01729]embedded image (500 MHz, Chloroform-d) δ 8.41 (s, 2H), 7.23 (s, 1H), 3.97 (s, 3H), 2.85 (t, J = 8.0 Hz, 2H), 1.94-1.78 (m, 2H), 1.37 -1.24(m, 6H), 0.93 (t, J = 8.0 Hz, 3H). 1-53 CF.sub.3 [01730]embedded image [01731]embedded image (500 MHz, Chloroform-d) δ 7.67 (d, J = 2.0 Hz, 1H), 7.34- 7.23 (m, 2H), 7.21 (s, 1H), 2.85 (t, J = 8.0 Hz, 2H), 1.94- 1.80 (m, 2H), 1.38-1.22 (m, 8H), 0.93 (t, J = 8.0 Hz, 3H). 1-54 CF.sub.3 [01732]embedded image [01733]embedded image (500 MHz, Chloroform-d) δ 7.48-7.32 (m, 2H), 7.11- 6.93 (m, 3H), 2.85 (t, J = 8.0 Hz, 2H), 1.94-1.81 (m, 2H), 1.37- 1.20 (m, 10H), 0.94 (t, J = 8.0 Hz, 3H). 1-55 CF.sub.3 [01734]embedded image [01735]embedded image (500 MHz, Chloroform-d) δ 7.26 (s, 1H), 7.21-7.11 (m, 3H), 2.85 (t, J = 8.0 Hz, 2H), 1.94-1.81 (m, 2H), 1.38- 1.20 (m, 10H), 0.93 (t, J = 8.0 Hz, 3H). 1-56 CF.sub.3 [01736]embedded image [01737]embedded image (500 MHz, Chloroform-d) δ 7.47 (d, J = 7.5 Hz, 2H), 7.23 (d, J = 7.5 Hz, 2H), 2.85 (t, J = 8.0 Hz, 2H), 2.33 (s, 3H), 1.94 -1.81 (m, 2H), 1.38-1.20 (m, 14H), 0.93 (t, J = 8.0 Hz, 3H). 1-57 CF.sub.3 [01738]embedded image [01739]embedded image (500 MHz, Chloroform-d) δ 7.61 (d, J = 7.5 Hz, 2H), 7.41 (d, J = 7.5 Hz, 2H), 7.11 (s, 1H), 3.11 (s, 3H), 2.85 (t, J = 8.0 Hz, 1H), 1.94-1.81 (m, 2H), 1.47-1.20 (m, 18H), 0.92 (t, J = 8.0 Hz, 3H). 1-58 CF.sub.3 [01740]embedded image [01741]embedded image (500 MHz, Chloroform-d) δ 7.57-7.50 (m, 2H), 7.46- 7.37 (m, 3H), 7.32 (s, 1H), 2.93-2.81 (m, 1H), 1.79- 1.62 (m, 4H), 1.42-1.15 (m, 6H). 1-59 CF.sub.3 [01742]embedded image [01743]embedded image 1-60 CF.sub.3 [01744]embedded image [01745]embedded image (500 MHz, Chloroform-d) δ 7.37-7.21 (m, 2H), 7.18 (s, 1H), 7.13-7.01 (m, 1H), 3.14 (s, 3H), 3.04 (s, 3H). 1-61 CF.sub.3 [01746]embedded image [01747]embedded image (500 MHz, Chloroform-d) δ 7.60 (d, J = 7.5 Hz, 2H), 7.53 (d, J = 7.5 Hz, 2H), 7.15 (s, 1H), 3.48 (q, 7 = 8.0 Hz, 4H), 1.23 (t, J = 8.0 Hz, 6H). 1-62 CF.sub.3 [01748]embedded image [01749]embedded image (500 MHz, Chloroform-d) δ 7.33-7.21 (m, 1H), 7.17- 7.04 (m, 2H), 3.58 (s, 3H), 3.44 (s, 3H). 1-63 CF.sub.3 [01750]embedded image [01751]embedded image (500 MHz, Chloroform-d) δ 7.42-7.34 (m, 2H), 7.16 (s, 1H), 7.11-7.03 (m, 2H), 3.57 (q, J = 8.0 Hz, 2H), 3.44 (s, 3H), 1.21 (t, J = 8.0 Hz, 3H). 1-64 CF.sub.3 [01752]embedded image [01753]embedded image (500 MHz, Chloroform-d) δ 7.46-7.38 (m, 2H), 7.17 (s, 1H), 7.11-7.03 (m, 2H), 3.47 -3.30 (m,4H), 3.19-3.04 (m, 4H), 2.32 (s, 3H). 1-65 CF.sub.3 [01754]embedded image [01755]embedded image (500 MHz, Chloroform-d) δ 7.53-7.45 (m, 2H), 7.41- 7.22 (m, 3H),7.16(s, 1H), 3.64-3.49 (m, 4H), 3.47- 3.32 (m, 4H). 1-66 CF.sub.3 [01756]embedded image [01757]embedded image (500 MHz, Chloroform-d) δ 7.38-7.24 (m, 1H), 7.23- 7.13 (m, 3H), 3.84-3.66 (m, 4H), 3.47-3.33 (m, 4H). 1-67 CF.sub.3 [01758]embedded image [01759]embedded image (500 MHz, Chloroform-d) δ 7.44-7.37 (m, 2H), 7.17 (s, 1H), 7.11-7.03 (m, 2H), 3.90 -3.77 (m,4H), 1.79- 1.65 (m, 6H). 1-68 CF.sub.3 [01760]embedded image [01761]embedded image (500 MHz, Chloroform-d) δ 7.57-7.43 (m, 2H), 7.46- 7.37 (m, 2H), 7.32 (s, 1H), 3.84-3.66 (m, 4H), 3.47- 3.33 (m, 4H) 1-69 CF.sub.3 [01762]embedded image [01763]embedded image (500 MHz, Chloroform-d) δ 7.52-7.44 (m, 2H), 7.18 (s, 1H), 7.11-7.03 (m, 2H), 3.46 -3.23 (m, 2H), 2.16 v 2.02 (m, 2H), 1.92-1.77 (m, 4H). 1-70 CF.sub.3 [01764]embedded image [01765]embedded image (500 MHz, Chloroform-d) δ 7.51-7.44 (m, 2H), 7.27 (s, 1H), 7.11-7.03 (m, 2H), 3.64 (s, 3H), 2.34-2.22 (m, 4H), 1.77-1.67 (m, 2H), 1.65- 1.55 (m, 2H). 1-71 CF.sub.3 [01766]embedded image [01767]embedded image (500 MHz, Chloroform-d) δ 7.43-7.28 (m, 2H), 7.23- 7.16 (m, 1H), 7.14 (s, 1H), 4.31 (s, 2H), 3.30 (s, 3H). 1-72 CF.sub.3 [01768]embedded image [01769]embedded image (500 MHz, Chloroform-d) δ 7.57-7.41 (m, 2H), 4.07 (q, J = 8.0 Hz, 1H), 2.34 (t, J = 7.5 Hz, 2H), 2.05 (d, J = 8.0 Hz, 2H), 1.17-1.05 (m, 2H). 1-73 CF.sub.3 [01770]embedded image [01771]embedded image (500 MHz, Chloroform-d) δ 7.68 (d, J = 7.5 Hz, 2H), 7.57 (d, J = 7.5 Hz, 2H), 7.22 (s, 1H), 4.22 (q, J = 8.0 Hz, 2H), 1.31 (t, J = 8.0 Hz, 3H). 1-74 CF.sub.3 [01772]embedded image [01773]embedded image (500 MHz, Chloroform-d) δ 7.53-7.48 (m, 1H), 7.47- 7.40 (m, 2H), 7.31-7.18 (m, 2H), 4.23 (s, 2H), 2.71 (d, J = 8.0 Hz, 2H), 2.02 (s, 3H), 1.21 (t, J = 8.0 Hz, 3H), 1.19 (s, 6H). 1-75 CF.sub.3 [01774]embedded image [01775]embedded image (500 MHz, Chloroform-d) δ 7.48-7.40 (m, 1H), 7.32- 7.21 (m, 3H), 7.03-6.90 (m, 1H), 4.79-4.66 (m, 1H), 4.06 (q, J = 8.0 Hz, 2H), 1.21 (t, J = 8.0 Hz, 3H). 1-76 CF.sub.3 [01776]embedded image [01777]embedded image (500 MHz, Chloroform-d) δ 7.48-7.40 (m, 2H), 7.20 (s, 1H), 7.11-7.03 (m, 2H), 3.39 (s, 2H), 2.05 (s, 3H). 1-77 CF.sub.3 [01778]embedded image [01779]embedded image (500 MHz, Chloroform-d) δ 7.40-7.29 (2, 1H), 7.23-7.10 (m, 2H), 2.71 (t, J = 8.0 Hz, 2H), 2.60 (t, J = 8.0 Hz, 2H), 2.14 (s, 3H). 1-78 CF.sub.3 [01780]embedded image [01781]embedded image (500 MHz, Chloroform-d) δ 7.42-7.34 (m, 2H), 7.16 (s, 1H), 7.11-7.03 (m, 2H), 3.46 -3.30 (m, 2H), 2.73-2,66 (m, 2H), 2.19-2.09 (m, 1H), 1.79 (s, 2H), 1.26 (s, 3H). 1-79 CF.sub.3 [01782]embedded image [01783]embedded image (500 MHz, Chloroform-d) δ 8.16-8.09 (m, 2H), 7.67- 7.55 (m, 3H), 7.37-7.18 (m, 2H), 7.14-7.00 (m, 3H). 1-80 CF.sub.3 [01784]embedded image [01785]embedded image (500 MHz, Chloroform-d) δ 7.49-7.35 (m, 4H), 7.36- 7.26 (m, 2H), 7.26-7.18 (m, 3H), 2.52 (s, 3H), 2.33 (s, 3H). 1-81 CF.sub.3 [01786]embedded image [01787]embedded image (500 MHz, Chloroform-d) δ 8.05-7.99 (m, 2H), 7.51- 7.41 (m, 3H), 7.24 (s, 1H), 7.21-7.13 (m, 2H), 2.50 (s, 3H), 2.41 (s, 3H), 2.30 (s, 3H). 1-82 CF.sub.3 [01788]embedded image [01789]embedded image (500 MHz, Chloroform-d) δ 8.05-7.89 (m, 4H), 7.76- 7.59 (m, 4H), 7.25 (s, 1H). 1-83 CF.sub.3 [01790]embedded image [01791]embedded image (500 MHz, Chloroform-d) δ 7.59-7.52 (m, 2H), 7.49- 7.40 (m, 5H), 7.33 (s, 1H), 7.32-7.28 (m, 1H). 1-84 CF.sub.3 [01792]embedded image [01793]embedded image (500 MHz, Chloroform-d) δ 8.12-8.06 (m, 2H), 7.37- 7.19 (m, 3H), 7.15-7.03 (m, 3H), 3.80 (s, 3H). 1-85 CF.sub.3 [01794]embedded image [01795]embedded image (500 MHz, Chloroform-d) δ 7.93-7.58 (m, 2H), 7.46- 7.39 (m, 2H), 7.23 (s, 1H),7.11 -7.03 (m, 4H),5.19(s, 1H). 1-86 CF.sub.3 [01796]embedded image [01797]embedded image (500 MHz, Chloroform-d) δ 7.90 (dd, J = 7.5, 2.0 Hz, 1H), 7.81-7.73 (m, 2H), 7.75- 7.68 (m, 1H), 7.44 (s, 1H), 7.39-7.16(m, 3H). 1-87 CF.sub.3 [01798]embedded image [01799]embedded image (500 MHz, Chloroform-d) δ 8.10 (dd, J = 7.5, 2.0 Hz, 1H), 7.60-7.43 (m, 3H), 7.46- 7.37 (m, 3H), 7.25-7.15 (m, 2H), 2.39 (s, 3H). 1-88 CF.sub.3 [01800]embedded image [01801]embedded image (500 MHz, Chloroform-d) δ 7.83-7.68 (m, 2H), 7.52- 7.33 (m, 4H), 7.27-7.21 (m, 3H). 1-89 CF.sub.3 [01802]embedded image [01803]embedded image (500 MHz, Chloroform-d) δ 7.96-7.89 (m, 2H), 7.85- 7.79 (m, 2H), 7.73 (s, 1H), 7.46-7.38 (m, 2H), 7.33- 7.26 (m, 2H), 7.22 (s, 1H), 2.71 (q, J = 8.0 Hz, 2H), 2.10 (s, 3H), 1.21 (t, J = 8.0 Hz, 3H). 1-90 CF.sub.3 [01804]embedded image [01805]embedded image (500 MHz, Chloroform-d) δ 7.71-7.65 (m, 2H), 7.48- 7.34 (m, 2H), 7.25-7.20 (m, 3H), 6.82-6.75 (m, 2H), 3.02 (s, 6H). 1-91 CF.sub.3 [01806]embedded image [01807]embedded image (500 MHz, Chloroform-d) δ 7.57 (d, J = 2.0 Hz, 1H), 7.50- 7.36 (m, 4H), 7.33 (s, 1H),7.11 -7.03 (m, 2H). 1-92 CF.sub.3 [01808]embedded image [01809]embedded image (500 MHz, Chloroform-d) δ 8.24 (d, J = 2.0 Hz, 1H), 7.73 (dd, J = 7.5, 2.0 Hz, 1H), 7.54 (d, J = 7.5 Hz, 1H), 7.52 (d, J = 7.5 Hz, 2H), 7.25 (s, 1H), 7.13 (d, J = 7.5 Hz, 2H), 2.77 (d, J = 8.0 Hz, 2H), 1.19 (t, J = 8.0 Hz, 3H). 1-93 CF.sub.3 [01810]embedded image [01811]embedded image (500 MHz, Chloroform-d) δ 7.53-7.45 (m, 2H), 7.41- 7.32 (m, 2H), 7.25 (s, 1H), 7.15-7.03 (m, 2H). 1-94 CF.sub.3 [01812]embedded image [01813]embedded image (500 MHz, Chloroform-d) δ 7.31-7.27 (m, 3H), 7.31- 7.24 (m, 1H), 7.27-7.18 (m, 3H), 7.17-7.08 (m, 2H), 3.92 (s, 2H). 1-95 CF.sub.3 [01814]embedded image [01815]embedded image (500 MHz, Chloroform-d) δ 7.53-7.46 (m, 3H), 7.43- 7.31 (m, 3H), 7.25-7.15 (m, 3H), 3.54 (s, 2H). 1-96 CF.sub.3 [01816]embedded image [01817]embedded image (500 MHz, Chloroform-d) δ 7.59-7.41 (m, 5H), 7.39- 7.27 (m, 5H), 7.16 (s, 1H), 5.90 (d, J = 10.5 Hz, 1H). 1-97 CF.sub.3 [01818]embedded image [01819]embedded image (500 MHz, Chloroform-d) δ 7.50-7.42 (m, 4H), 7.45- 7.35 (m, 5H), 7.11-7.00 (d, J = 11.0 Hz, 1H),5.87 (d, J = 11.0 Hz, 1H). 1-98 CF.sub.3 [01820]embedded image [01821]embedded image (500 MHz, Chloroform-d) δ 7.62-7.55 (m, 2H), 7.47- 7.38 (m, 4H), 7.34 (s, 1H), 7.11 -7.03 (m, 2H),5.99 (s, 2H). 1-99 CF.sub.3 [01822]embedded image [01823]embedded image (500 MHz, Chloroform-d) δ 7.40-7.30 (m, 3H), 7.29- 7.18 (m, 3H), 7.21 (s, 1H), 6.99-6.87 (m, 3H), 3.10 (t, J = 8.0 Hz, 2H), 3.00 (t, J = 8.0 Hz, 2H). 1-100 CF.sub.3 [01824]embedded image [01825]embedded image (500 MHz, Chloroform-d) δ 7.48-7.40 (m, 3H), 7.24- 7.16 (m, 3H), 7.11-7.03 (m, 3H), 5.69 (s, 2H), 5.56 (s, 2H). 1-101 CF.sub.3 [01826]embedded image [01827]embedded image (500 MHz, Chloroform-d) δ 7.51-7.38 (m, 3H), 7.25- 7.14 (m, 3H),7.17(s, 1H), 7.08-7.00 (m, 2H), 4.52 (s, 2H), 4.31 (s, 3H). 1-102 CF.sub.3 [01828]embedded image [01829]embedded image (500 MHz, Chloroform-d) δ 7.49-7.41 (m, 3H), 7.21 (s, 1H), 7.11-7.03 (m, 2H), 6.89 -6.81 (m, 4H). 1-103 CF.sub.3 [01830]embedded image [01831]embedded image (500 MHz, Chloroform-d) δ 7.58-7.46 (m, 3H), 7.32- 7.20 (m, 5H), 7.19-7.07 (m, 2H), 3.70 (t, J = 8.0 Hz, 2H), 2.90 (t, J = 8.0 Hz, 2H), 2.70 (s, 3H). 1-104 CF.sub.3 [01832]embedded image [01833]embedded image (500 MHz, Chloroform-d) δ 7.57-7.51 (m, 2H), 7.52- 7.45 (m, 2H), 7.33 (s, 1H), 7.27 (s, 1H), 7.28-7.16 (m, 1H). 1-105 CF.sub.3 [01834]embedded image [01835]embedded image (500 MHz, Chloroform-d) δ 7.55 (dd, J = 7.5, 1.5 Hz, 1H), 7.42-7.33 (m, 3H), 7.24 (s, 1H), 7.28-7.16 (m, 3H), 6.48 (t, J = 7.5 Hz, 1H), 3.68 (s, 3H). 1-106 CF.sub.3 [01836]embedded image [01837]embedded image (500 MHz, Chloroform-d) δ 7.63 (d, J = 7.5 Hz, 2H), 7.41- 7.34 (m, 2H), 7.24 (s, 1H), 7.15-7.02 (m, 2H), 6.47- 6.38 (m, 1H). 1-107 CF.sub.3 [01838]embedded image [01839]embedded image (500 MHz, Chloroform-d) δ 8.11-8.06 (m, 1H), 7.57- 7.50 (m, 2H), 7.33-7.27 (m, 1H), 7.25 (s, 1H), 2.62 (s, 3H). 1-108 CF.sub.3 [01840]embedded image [01841]embedded image (500 MHz, Chloroform-d) δ 7.42-7.28 (m, 2H), 7.24 (s, 1H), 7.20-7.09 (m, 1H), 6.58 (s, 1H), 2.42 (s, 3H). 1-109 CF.sub.3 [01842]embedded image [01843]embedded image (500 MHz, Chloroform-d) δ 8.19-8.07 (m, 1H), 7.43- 7.27 (m, 3H), 7.24 (s, 1H), 7.20-7.06 (m, 2H). 1-110 CF.sub.3 [01844]embedded image [01845]embedded image (500 MHz, Chloroform-d) δ 8.37 (d, J = 2.5 Hz, 1H), 7.36- 7.28 (m, 2H), 7.22 (s, 1H),7.11 -7.03 (m, 2H), 6.80 (d, J = 7.5 Hz, 1H). 1-111 CF.sub.3 [01846]embedded image [01847]embedded image (500 MHz, Chloroform-d) δ 8.75 (d, J = 1.3 Hz, 1H), 7.70 (d, J = 8.0 Hz, 2H), 7.38 (d, J = 8.0 Hz, 2H). 1-112 CF.sub.3 [01848]embedded image [01849]embedded image (500 MHz, Chloroform-d) δ 9.21 (s, 1H), 8.79 (d, J = 5.5 Hz, 1H), 8.73 (d, J = 5.5 Hz, 1H), 7.24-7.13 (m, 4H). 1-113 CF.sub.3 [01850]embedded image [01851]embedded image (500 MHz, Chloroform-d) δ 8.56 (dd, J = 5.0, 1.0 Hz, 1H), 7.80 (dd, J = 8.0, 1.0 Hz, 1H), 7.37 (dd, J = 8.0, 5.0 Hz, 1H), 7.30-7.23 (m, 2H), 7.18- 7.13 (m, 2H), 2.97 (q, J = 8.0 Hz, 2H), 1.39 (t, J = 8.0 Hz, 3H) 1-114 CF.sub.3 [01852]embedded image [01853]embedded image (500 MHz, Chloroform-d) δ 8.12-8.02 (m, 2H), 8.08- 7.99 (m, 2H), 8.00-7.94 (m, 1H), 7.73-7.64 (m, 2H), 7.49 -7.41 (m, 2H),7.26 (s, 1H), 7.11-7.03 (m, 2H) 1-115 CF.sub.3 [01854]embedded image [01855]embedded image (500 MHz, Chloroform-d) δ 8.66-8.59 (m, 2H), 7.97 (dd, J = 7.5, 1.5 Hz, 1H), 7.62 (d, J = 7.5 Hz, 1H), 7.46-7.40 (m, 1H), 7.32-7.25 (m,2H), 7.26 -7.15 (m, 2H), 6.66-6.52 (m, 1H). 1-116 CF.sub.3 [01856]embedded image [01857]embedded image (500 MHz, Chloroform-d) δ 8.33-8.05 (m, 3H), 7.92 (d, J = 7.5, 1.5 Hz, 1H), 7.77-7.67 (m, 2H), 7.54-7.48 (m, 2H), 7.45-7.39 (m, 2H), 7.27 (s, 1H). 1-117 CF.sub.3 [01858]embedded image [01859]embedded image (500 MHz, Chloroform-d) δ 8.23-8.04 (m, 2H), 7.92 (d, J = 7.5 Hz, 1H), 7.75 (d, J = 7.5 Hz, 1H), 7.56-7.48 (m, 2H), 7.41-7.30 (m, 3H), 7.25 (s, 1H), 6.86 (dd, J = 7.5, 1.5 Hz, 1H). 1-118 CF.sub.3 [01860]embedded image [01861]embedded image (500 MHz, Chloroform-d) δ 7.77 (dd, J = 7.0, 2.5 Hz, 1H), 7.72 (d, J = 7.5 Hz, 2H), 7.62- 7.56 (m, 2H), 7.24 (s, 1H), 7.19-7.10 (m, 2H), 5.99 (s, 2H). 1-119 CF.sub.3 [01862]embedded image [01863]embedded image (500 MHz, Chloroform-d) δ 8.11-8.02 (m,2H), 7.59- 7.41 (m, 1H), 7.50-7.40 (m, 3H), 7.36-7.30 (m, 2H), 7.11 -7.03 (m, 2H). 1-120 CF.sub.3 [01864]embedded image [01865]embedded image (500 MHz, Chloroform-d) δ 7.65-7.58 (m, 2H), 7.54 (d, J = 1.5 Hz, 1H), 7.44-7.33 (m, 2H), 7.32-7.24 (m, 1H), 7.28 (s, 1H), 7.26-7.15 (m, 2H). 1-121 CF.sub.3 [01866]embedded image [01867]embedded image (500 MHz, Chloroform-d) δ 7.62 (s, 1H), 7.51-7.44 (m, 2H), 7.11-7.03 (m, 2H), 3.07 (q, J = 8.0 Hz, 2H), 1.50 (t, J = 8.0 Hz, 3H). 1-122 CF.sub.3 [01868]embedded image [01869]embedded image (500 MHz, Chloroform-d) δ 7.77 (d, J = 7.5 Hz, 2H), 7.57- 7.50 (m, 3H), 1.72-1.61 (m, 1H), 0.81-0.73 (m, 2H), 0.58 -0.51 (m,2H). 1-123 CF.sub.3 [01870]embedded image [01871]embedded image (500 MHz, Chloroform-d) δ 7.66-7.52 (m, 2H), 7.46- 7.39 (m, 2H), 7.34-7.29 (m, 1H), 5.15 (s, 2H), 3.05 (s, 3H), 2.71 (d, J = 8.0 Hz,2H), 1.21 (t, J = 8.0 Hz, 3H). 1-124 CF.sub.3 [01872]embedded image [01873]embedded image (500 MHz, Chloroform-d) δ 7.63-7.59 (m, 2H), 7.45- 7.33 (m, 2H), 7.25-7.18 (m, 1H), 4.45 (s, lH),3.75 (t, J = 7.5 Hz, 2H), 2.63 (t, J = 7.5 Hz, 2H), 1.83- 1.68 (m, 2H). 1-125 CF.sub.3 [01874]embedded image [01875]embedded image (500 MHz, Chloroform-d) δ 7.57 (s, 1H), 7.45-7.37 (m, 2H), 7.11-7.03 (m, 2H), 2.50 -2.38 (m, 8H), 2.27 (s, 3H). 1-126 CF.sub.3 [01876]embedded image [01877]embedded image (500 MHz, Chloroform-d) δ 7.76-7.70(m, 2H), 7.61 (s, 1H), 7.49-7.43 (m, 2H), 7.41 -7.30 (m, 1H), 7.20-7.10 (m, 2H), 2.42 (s, 3H). 1-127 CF.sub.3 [01878]embedded image [01879]embedded image (500 MHz, Chloroform-d) δ 7.78 (d, J = 7.5 Hz, 2H), 7.64 (s, 1H), 7.56-7.41 (m, 1H), 7.51-7.42 (m,2H), 7.19- 7.10 (m, 2H). 1-128 CF.sub.3 [01880]embedded image [01881]embedded image (500 MHz, Chloroform-d) δ 7.78-7.64 (m, 2H), 7.56- 7.41 (m, 1H), 7.51-7.42 (m, 2H), 7.19-7.10 (m,2H). 1-129 CF.sub.3 [01882]embedded image [01883]embedded image (500 MHz, Chloroform-d) δ 7.86 (d, J = 7.5 Hz, 2H), 7.76 (d, J = 7.5 Hz, 2H), 7.59 (s, 1H), 7.42-7.34 (m, 1H),7.16 -7.07 (m, 2H). 1-130 CF.sub.3 [01884]embedded image [01885]embedded image (500 MHz, Chloroform-d) δ 7.91 (d, J = 7.5 Hz, 2H), 7.78 (d, J = 7.5 Hz, 2H), 7.59 (s, 1H), 7.45-7.38 (m, 1H), 7.26 -7.17 (m, 2H). 1-131 CF.sub.3 [01886]embedded image [01887]embedded image (500 MHz, Chloroform-d) δ 7.70 (s, 1H), 7.64-7.57 (m, 2H), 7.41-7.31 (m, 3H), 7.08 (s, 2H), 2.55 (s, 6H), 2.13 (s, 3H). 1-132 CF.sub.3 [01888]embedded image [01889]embedded image (500 MHz, Chloroform-d) δ 7.76-7.70 (m, 2H), 7.58 (s, 1H), 7.45 (ddd, J = 7.6, 6.2, 2.1 Hz, 4H), 7.11-7.03 (m, 2H), 2.42 (d, J = 1.5 Hz, 2H). 1-133 CF.sub.3 [01890]embedded image [01891]embedded image (500 MHz, Chloroform-d) δ 7.83 (d, J = 2.0 Hz, 1H), 7.71- 7.63 (m, 2H), 7.55-7.47 (m, 3H), 7.11-7.03 (m, 2H). 1-134 CF.sub.3 [01892]embedded image [01893]embedded image (500 MHz, Chloroform-d) δ 7.84-7.76 (m, 2H), 7.59 (s, 1H), 7.49-7.41 (m, 2H),7.33 -7.24 (m, 2H), 7.11-7.03 (m, 2H). 1-135 CF.sub.3 [01894]embedded image [01895]embedded image (500 MHz, Chloroform-d) δ 8.46(d, J = 7.5Hz, 2H), 8.07 (d, J = 7.5 Hz, 2H), 7.58 (s, 1H), 7.32-7.22 (m, 3H). 1-136 CF.sub.3 [01896]embedded image [01897]embedded image (500 MHz, Chloroform-d) δ 8.32 (s, 1H), 8.08 (s, 1H), 7.60 -7.50 (m, 3H), 7.41-7.30 (m, 3H). 1-137 CF.sub.3 [01898]embedded image [01899]embedded image (500 MHz, Chloroform-d) δ 8.17-8.11 (m, 2H), 8.12- 8.05 (m, 2H), 7.53 (s, 1H), 7.46-7.38 (m,2H), 7.11- 7.03 (m, 2H), 3.30 (s, 3H). 1-138 CF.sub.3 [01900]embedded image [01901]embedded image (500 MHz, Chloroform-d) δ 7.61 (s, 1H), 7.64-7.57 (m, 1H), 7.52-7.39 (m, 2H), 7.28 -7.17 (m, 2H). 1-139 CF.sub.3 [01902]embedded image [01903]embedded image (500 MHz, Chloroform-d) δ 7.60-7.50 (m, 3H), 7.43 (d, J = 7.5 Hz, 2H), 7.40 (dd, J = 2.5, 1.5 Hz, 1H), 7.32-7.26 (m, 2H), 7.18 (s, 1H), 7.43 (t, J = 73.5 Hz, 1H). 1-140 CF.sub.3 [01904]embedded image [01905]embedded image (500 MHz, Chloroform-d) δ 8.33-8.28 (m, 2H), 8.17- 8.06 (m, 1H), 7.73-6.65 (m, 1H), 7.60-7.51 (m, 3H), 7.41 -7.30 (m, 3H), 2.60 (s, 3H). 1-141 CF.sub.3 [01906]embedded image [01907]embedded image (500 MHz, Chloroform-d) δ 8.10 (d, J = 7.5 Hz, 2H), 8.04 (d, J = 7.5 Hz, 2H), 7.69 (d, J = 7.5 Hz, 2H), 7.57 (d, J = 7.5 Hz, 2H), 7.17 (s, 1H), 6.41 (s, 2H). 1-142 CF.sub.3 [01908]embedded image [01909]embedded image (500 MHz, Chloroform-d) δ 7.79-7.70 (m, 3H), 7.45- 7.38 (m, 2H), 7.31-7.19 (m, 3H), 7.18-7.12 (m, 2H), 7.12 -7.04 (m, 2H). 1-143 CF.sub.3 [01910]embedded image [01911]embedded image (500 MHz, Chloroform-d) δ 7.60 (s, 1H), 7.53-7.45 (m, 2H), 7.30-7.20 (m, 5H), 7.11 -7.03 (m, 2H), 4.29 (s, 2H). 1-144 CF.sub.3 [01912]embedded image [01913]embedded image (500 MHz, Chloroform-d) δ 8.80 (dd, J = 7.5, 1.5 Hz, 1H), 8.26-8.15 (m, 2H), 8.01- 7.78 (m, 2H), 7.58-7.50 (m, 4H), 7.51-7.40 (m, 3H). 1-145 CF.sub.3 [01914]embedded image [01915]embedded image (500 MHz, Chloroform-d) δ 8.16 (d, J = 2.5 Hz, 1H), 7.75- 7.69 (m, 2H), 7.47-7.36 (m, 3H), 7.33-7.24 (m, 1H), 2.71 -2.61 (d, J = 8.0 Hz, 2H), 1.21 (t, J = 8.0 Hz, 3H). 1-146 CF.sub.3 [01916]embedded image [01917]embedded image (500 MHz, Chloroform-d) δ 8.41 (d, J = 1.5 Hz, 1H),7.99 (dd, J = 8.0, 1.5 Hz, 1H), 7.63 (s, 1H), 7.50-7.39 (m, 4H), 7.32-7.21 (m, 2H), 7.18- 7.08 (m, 3H), 6.96(dd, J = 7.5, 2.0 Hz, 1H). 1-147 CF.sub.3 [01918]embedded image [01919]embedded image (500 MHz, Chloroform-d) δ 9.38 (s, 1H), 8.81 (d, J = 1.5 Hz, 1H), 7.99-7.91 (m, 2H), 7.63 (s, 1H), 7.48-7.25 (m, 3H). 1-148 CF.sub.3 [01920]embedded image [01921]embedded image (500 MHz, Chloroform-d) δ 8.43 (d, J = 1.5 Hz, 1H), 8.15 (dd, J = 2.5,1.5 Hz, 1H), 7.85 (dd, J = 7.5,1.5 Hz, 1H), 7.77 -7.60 (m, 3H), 7.56-7.49 (m, 3H). 1-149 CF.sub.3 [01922]embedded image [01923]embedded image (500 MHz, Chloroform-d) δ 7.97 (dd, J = 6.5, 2.0 Hz, 1H), 7.70-7.65 (m, 2H), 7.61 (d, J = 1.5 Hz, 1H), 7.53-7.43 (m, 3H), 7.37-7.27 (m, 3H), 2.71 -2.62 (d, J = 8.0 Hz, 2H), 1.21 (t, J = 8.0 Hz, 3H). 1-150 CF.sub.3 [01924]embedded image [01925]embedded image (500 MHz, Chloroform-d) δ 7.73 (s, 1H), 7.59-7.49 (m, 2H), 7.36 (d, J = 2.5 Hz, 1H), 7.31-7.25 (m, 3H), 3.66 (s, 3H). 1-151 CF.sub.3 [01926]embedded image [01927]embedded image (500 MHz, Chloroform-d) δ 7.73-7.65 (m, 2H), 7.62 (s, 1H), 7.57-7.42 (m, 2H), 7.25 -7.19 (m,2H), 3.92 (s, 3H). 1-152 CF.sub.3 [01928]embedded image [01929]embedded image (500 MHz, Chloroform-d) δ 7.93-7.85 (m, 2H), 7.80 (dd, J = 7.5, 1.5 Hz, 1H), 7.72 (s, lH),7.33-7.19(m, 3H),7.11 (d, J = 7.5 Hz, 1H), 6.50 (dd, J = 7.5, 1.5 Hz, 1H), 3.80 (s, 3H). 1-153 CF.sub.3 [01930]embedded image [01931]embedded image (500 MHz, Chloroform-d) δ 7.76-7.60 (m, 4H), 7.56- 7.44 (.sub.m, 4H), 7.26-7.14 (m, 2H), 2.66 (q, J = 8.0 Hz, 1H), 1.21 (t, J = 8.0 Hz, 1H). 1-154 CF.sub.3 [01932]embedded image [01933]embedded image (500 MHz, Chloroform-d) δ 7.45 (dd, J = 7.5, 5.5 Hz, 2H), 7.28 (s, 1H),7.07(dd, J = 9.0, 7.5 Hz, 2H), 1.41 (t, J = 8.0 Hz, 2H), 1.36-1.22 (m, 12H), 0.93 (t, J = 8.0 Hz, 3H). 1-155 CF.sub.3 [01934]embedded image [01935]embedded image (500 MHz, Chloroform-d) δ 7.44 (d, J = 7.5 Hz, 2H), 7.22- 7.13 (m,3H), 3.62 (q,7 = 8.0 Hz, 2H), 2.33 (s, 3H), 1.36 (t, J = 8.0 Hz, 3H). 1-156 CF.sub.3 [01936]embedded image [01937]embedded image (500 MHz, Chloroform-d) δ 7.50(d, J = 7.5 Hz, 2H), 7.21 (s, 1H), 6.80 (d, J = 7.5 Hz, 2H), 3.80 (s, 3H),3.60(t, J = 7.5 Hz, 2H), 1.78-1.66 (m, 2H), 1.01 (t, J = 8.0 Hz, 3H). 1-157 CF.sub.3 [01938]embedded image [01939]embedded image (500 MHz, Chloroform-d) δ 7.30-7.22 (m, 2H), 7.20 (s, 1H), 7.15-7.05 (m, 1H), 3.65 (t, J = 8.0 Hz, 2H), 1.46-1.36 (m, 4H), 1.03 (t, J = 8.0 Hz, 3H). 1-158 CF.sub.3 [01940]embedded image [01941]embedded image (500 MHz, Chloroform-d) δ 7.52-7.43 (m, 2H), 7.34 (s, 1H), 7.27 (dd, J = 7.5, 2.0 Hz, 1H), 3.45 (d, J = 7.0 Hz, 2H), 1.49-1.38 (m, 1H), 0.92 (d, J = 7.5 Hz, 6H). 1-159 CF.sub.3 [01942]embedded image [01943]embedded image (500 MHz, Chloroform-d) δ 7.84 (dd, J = 2.0 Hz, 1H), 7.62 (d, J = 7.5 Hz, 1H), 7.43-7.33 (m, 1H), 7.19 (s, 1H), 3.60 (t, J = 7.5 Hz, 2H), 2.50 (s, 3H), 1.67-1.60 (m, 1H), 1.43- 1.31 (m, 2H), 0.97 (d, J = 6.5 Hz, 6H). 1-160 CF.sub.3 [01944]embedded image [01945]embedded image (500 MHz, Chloroform-d) δ 7.31 (d, J = 7.5 Hz, 1H), 7.22 (s, 1H), 7.14 (d, J = 7.5 Hz, 1H), 3.60 (t, J = 7.0 Hz, 2H), 1.65-1.55 (m, 2H), 1.43- 1.31 (m, 6H), 0.89 (t, J = 7.5 Hz, 3H). 1-161 CF.sub.3 [01946]embedded image [01947]embedded image (500 MHz, Chloroform-d) δ 7.40-7.35 (m, 2H), 7.33- 7.15 (m, 3H), 3.88-3.73 (m, 1H), 2.65-2.55 (m, 2H), 1.69 -1.55 (m, 2H), 1.59-1.39 (m, 3H), 1.28-1.07 (m, 11H), 0.89 (t, J = 7.5 Hz, 3H). 1-162 CF.sub.3 [01948]embedded image [01949]embedded image (500 MHz, Chloroform-d) δ 7.45-7.37(m, 2H), 7.20 (s, 1H), 7.11-7.03 (m, 2H), 3.65 (q, J = 8.0 Hz, 4H), 1.17 (t, J = 8.0 Hz, 6H). 1-163 CF.sub.3 [01950]embedded image [01951]embedded image (500 MHz, Chloroform-d) δ 7.45-7.37 (m, 2H), 7.24- 7.11 (m, 2H), 2.85 (t, J = 8.0 Hz, 2H), 1.94-1.81 (m, 2H), 1.38-1.29 (m, 2H), 1.32- 1.20 (m, 8H), 0.93-0.85 (t, J = 8.0 Hz, 3H). 1-164 CF.sub.3 [01952]embedded image [01953]embedded image (500 MHz, Chloroform-d) δ 7.53-7.47 (m, 2H), 7.48- 7.40 (m, 2H), 7.28-7.20 (m, 3H), 7.11-7.03 (m, 3H). 1-165 CF.sub.3 [01954]embedded image [01955]embedded image (500 MHz, Chloroform-d) δ 7.40-7.28 (m, 2H), 7.19- 7.14 (m, 2H), 2.61 (q, J = 8.0 Hz, 2H), 1.35 (t, J = 8.0 Hz, 3H). 1-166 CF.sub.3 [01956]embedded image [01957]embedded image (500 MHz, Chloroform-d) δ 7.45-7.37(m, 2H), 7.28 (s, 1H), 7.11-7.03 (m, 2H). 1-167 CF.sub.3 [01958]embedded image [01959]embedded image (500 MHz, Chloroform-d) δ 7.58 (dd, J = 5.5, 2.0 Hz, 1H), 7.36-7.29 (m, 1H), 7.32 (s, lH),7.16(dd, J = 10.5, 7.5 Hz, 1H), 3.78 (s, 6H). 1-168 CF.sub.3 [01960]embedded image [01961]embedded image 1-169 CF.sub.3 [01962]embedded image [01963]embedded image (500 MHz, Chloroform-d) δ 7.38-7.30 (m, 1H), 7.25- 7.13 (m, 2H), 7.08 (s, 1H), 2.65 (s, 6H). 1-170 CF.sub.3 [01964]embedded image [01965]embedded image (500 MHz, Chloroform-d) δ 7.46 (d, J = 7.0 Hz, 2H), 7.20 (d, J = 7.0 Hz,2H),7.15(s, 1H), 2.59 (s, 3H), 2.33 (s, 3H), 2.17 (q, J = 8.0 Hz, 2H), 0.92 (t, J = 8.0 Hz, 3H). 1-171 CF.sub.3 [01966]embedded image [01967]embedded image (500 MHz, Chloroform-d) δ 7.49 (d, J = 7.5 Hz, 2H), 6.80- 6.74 (m, 3H), 3.80 (s, 3H), 2.58 (s, 3H), 2.11 (t, J = 7.5 Hz, 2H), 1.54-1.44 (m, 2H), 0.76 (t, J = 8.0 Hz, 3H). 1-172 CF.sub.3 [01968]embedded image [01969]embedded image (500 MHz, Chloroform-d) δ 7.47-7.40 (m, 2H), 7.15 (s, 1H), 7.11-7.03 (m, 2H), 6.87 (t, J = 7.0 Hz, 1H), 2.11-2.00 (m, 2H), 1.54-1.42 (m, 2H), 0.81 (t, J = 8.0 Hz, 3H). 1-173 CF.sub.3 [01970]embedded image [01971]embedded image (500 MHz, Chloroform-d) δ 7.95-7.89 (m, 2H), 7.72- 7.66 (m, 2H), 7.09 (s, 1H), 2.62 (s, 3H), 2.05 (d, J = 7.0 Hz, 2H), 1.77- 1.68 (m, 1H), 0.97 (d, J = 6.5 Hz, 6H). 1-174 CF.sub.3 [01972]embedded image [01973]embedded image (500 MHz, Chloroform-d) δ 7.41 (d, J = 2.0 Hz, 1H), 7.32 (dd, J = 7.5, 2.0 Hz, 1H), 7.15 (d, J = 7.5 Hz, 1H), 7.08 (s, 1H), 2.66 (s, 3H), 2.30 (s, 3H), 2.20 (s, 3H), 1.16 (s, 9H). 1-175 CF.sub.3 [01974]embedded image [01975]embedded image (500 MHz, Chloroform-d) δ 7.99 (d, J = 7.0 Hz, 2H), 7.87- 7.81 (m, 3H), 3.30 (s, 3H), 2.59 (s, 3H), 2.11 (t, J = 8.0 Hz, 2H), 1.55- 1.40 (m, 4H), 0.95 (t, J = 8.0 Hz, 3H). 1-176 CF.sub.3 [01976]embedded image [01977]embedded image (500 MHz, Chloroform-d) δ 7.54 (d, J = 2.0 Hz, 1H), 7.49 (d, J = 7.5 Hz, 1H), 7.34 (dd, J = 7.5, 2.0 Hz, 1H), 7.14 (s, 1H), 2.57 (s, 3H), 2.11 (t, J = 8.0 Hz, 2H), 1.55-1.47 (m, 2H), 1.34-1.23 (m, 6H), 0.93 (t, J = 8.0 Hz, 3H). 1-177 CF.sub.3 [01978]embedded image [01979]embedded image (500 MHz, Chloroform-d) δ 7.50 (d, J = 7.5 Hz, 2H), 7.19- 7.03 (m, 3H), 4.00 (t, J = 7.5 Hz, 2H), 2.21-2.07 (m, 4H), 1.60-1.44 (m, 8H), 1.36- 1.23 (m,5H), 1.04 (t, J = 8.0 Hz, 3H), 0.92 (t, J = 8.0 Hz, 3H). 1-178 CF.sub.3 [01980]embedded image [01981]embedded image (500 MHz, Chloroform-d) δ 8.43-8.25 (m, 2H), 7.91- 7.80 (m, 1H), 7.63-7.55 (m, 1H), 7.16 (s, 1H), 2.11 (t, J = 7.5 Hz, 4H), 1.55-1.40 (m, 8H), 0.95 (t, J = 8.0 Hz, 6H). 1-179 CF.sub.3 [01982]embedded image [01983]embedded image (500 MHz, Chloroform-d) δ 7.62 (d, J = 2.5 Hz, 1H), 7.30 (s, 1H), 6.45 (d, J = 2.5 Hz, 1H), 4.00 (s, 3H), 2.55-2.41 (m, 2H), 2.32-2.02 (m, 2H), 1.68- 1.57 (m, 1H), 1.37- 1.19 (m, 2H), 1.02-0.88 (m, 9H). 1-180 CF.sub.3 [01984]embedded image [01985]embedded image (500 MHz, Chloroform-d) δ 7.47 (d, J = 7.0 Hz, 2H), 7.17- 7.03 (m, 3H), 2.05 (d, J = 7.0 Hz, 4H), 1.72-1.60 (m, 2H), 0.96 (d, J = 6.5 Hz, 12H). 1-181 CF.sub.3 [01986]embedded image [01987]embedded image (500 MHz, Chloroform-d) δ 7.59-7.51 (m, 2H), 7.41- 7.33 (m, 3H), 7.16 (s, 1H), 2.59 (s, 3H), 2.40 (t, J = 7.5 Hz, 2H), 1.61-1.55 (m, 3H), 1.31-1.15 (m, 2H), 1.17- 1.09 (m, 1H), 1.12-1.02 (m, 2H), 0.85 (t, J = 7.5 Hz, 2H), 0.74 (d, J = 6.5 Hz, 3H). 1-182 CF.sub.3 [01988]embedded image [01989]embedded image (500 MHz, Chloroform-d) δ 7.35-7.27 (m, 2H),7.16(dd, J = 7.5, 1.0 Hz, 1H), 7.13 (s, 1H), 2.57 (s, 3H), 2.30 (s, 3H), 2.20 (s, 3H), 2.11 (t, J = 8.0 Hz, 2H), 1.55-1.22 (m, 14H), 0.89 (t, J = 8.0 Hz, 3H). 1-183 CF.sub.3 [01990]embedded image [01991]embedded image 1-184 CF.sub.3 [01992]embedded image [01993]embedded image 1-185 CF.sub.3 [01994]embedded image [01995]embedded image (500 MHz, Chloroform-d) δ 7.47-7.40 (m, 2H), 7.16 (s, 1H), 7.11-7.03 (m, 2H), 4.21 (s, 2H), 3.19(s, 3H), 2.57 (s, 3H). 1-186 CF.sub.3 [01996]embedded image [01997]embedded image (500 MHz, Chloroform-d) δ 7.44-7.37 (m, 1H), 7.25- 7.16 (m, 2H),7.16(s, 1H), 3.28 (s, 2H), 2.60 (s, 3H), 2.00 (s, 3H). 1-187 CF.sub.3 [01998]embedded image [01999]embedded image (500 MHz, Chloroform-d) δ 7.59-7.51 (m, 2H), 7.41- 7.27 (m, 3H),7.14(s, 1H), 2.73 (q, J = 6.5 Hz, 1H), 2.59 (s, 3H), 2.10 (s,3H), 1.31 (d, J = 6.5 Hz, 3H). 1-188 CF.sub.3 [02000]embedded image [02001]embedded image (500 MHz, Chloroform-d) δ 7.45 (d, J = 7.5 Hz, 2H), 7.25 (d, J = 7.5 Hz, 2H), 7.11 (s, 1H), 2.73 (q, J = 6.5 Hz, 1H), 2.59 (s, 3H), 2.19 (d, J = 8.0 Hz, 2H), 1.31 (d, J = 6.5 Hz, 3H) 1.24 (t, J = 8.0 Hz, 3H). 1-189 CF.sub.3 [02002]embedded image [02003]embedded image (500 MHz, Chloroform-d) δ 8.01-7.91 (m, 2H), 7.70- 7.53 (m, 2H), 7.19 (s, 1H), 3.28 (s, 2H), 2.60 (s, 3H), 2.48 (q, J = 8.0 Hz, 2H), 1.21 (t, J = 8.0 Hz, 3H). 1-190 CF.sub.3 [02004]embedded image [02005]embedded image (500 MHz, Chloroform-d) δ 7.46 (d, J = 7.0 Hz, 1H), 7.17- 7.10 (m, 3H), 2.75-2.63 (m, 4H), 2.59 (s, 3H), 2.49 (q, J = 8.0 Hz, 2H), 1.21 (t, J = 8.0 Hz, 3H). 1-191 CF.sub.3 [02006]embedded image [02007]embedded image 1-192 CF.sub.3 [02008]embedded image [02009]embedded image (500 MHz, Chloroform-d) δ 7.73 (d, J = 7.5 Hz, 1H), 7.60- 7.53 (m, 3H), 3.28 (s, 2H), 2.71 (t, J = 8.0 Hz, 1H), 2.58 (s, 3H), 1.38-1.20 (m, 12H), 0.93 (t, J = 8.0 Hz, 3H). 1-193 CF.sub.3 [02010]embedded image [02011]embedded image (500 MHz, Chloroform-d) δ 7.50-7.40 (m, 1H), 7.37- 7.28 (m, 2H), 7.22-7.17 (m, 1H), 7.11 (s, 1H), 2.71-2.62 (m, 4H), 2.17 (q, J = 8.0 Hz, 2H), 1.60-1.50 (m, 6H), 1.21 (t, J = 8.0 Hz, 3H). 1-194 CF.sub.3 [02012]embedded image [02013]embedded image (500 MHz, Chloroform-d) δ 7.53 (t, J = 7.0 Hz, 2H), 7.44 (t, J = 7.0 Hz, 2H), 7.15 (s, 1H), 2.66-2.53 (m, 4H), 2.50 -2.36 (m, 4H). 1-195 CF.sub.3 [02014]embedded image [02015]embedded image (500 MHz, Chloroform-d) δ 7.58-7.50 (m, 2H), 7.52- 7.39 (m, 4H), 7.33-7.26 (m, 2H),7.17(s, 1H), 7.11-7.03 (m, 2H). 1-196 CF.sub.3 [02016]embedded image [02017]embedded image (500 MHz, Chloroform-d) δ 7.50 (s, 5H), 7.53-7.40 (m, 1H), 7.28-7.19 (m, 2H), 7.15 (s, 1H), 3.08 (s, 3H). 1-197 CF.sub.3 [02018]embedded image [02019]embedded image 1-198 CF.sub.3 [02020]embedded image [02021]embedded image (500 MHz, Chloroform-d) δ 8.59-8.37 (m, 2H), 7.72- 7.49 (m, 4H), 7.41-7.33 (m, 4H),7.19(s, 1H), 7.11-7.03 (m, 2H). 1-199 CF.sub.3 [02022]embedded image [02023]embedded image (500 MHz, Chloroform-d) δ 7.52-7.44 (m, 2H), 7.38- 7.23 (m, 7H), 7.26-7.16 (m, 4H), 7.09 (s, 1H). 1-200 CF.sub.3 [02024]embedded image [02025]embedded image (500 MHz, Chloroform-d) δ 7.62-7.52 (m, 2H), 7.45- 7.37 (m, 1H), 7.32-7.19 (m, 4H), 7.13 (s, 1H), 2.36 (s, 3H). 1-201 CF.sub.3 [02026]embedded image [02027]embedded image 1-202 CF.sub.3 OEt [02028]embedded image 1-203 CF.sub.3 [02029]embedded image [02030]embedded image 1-204 CF.sub.3 [02031]embedded image [02032]embedded image 1-205 CF.sub.3 [02033]embedded image [02034]embedded image 1-206 CF.sub.3 [02035]embedded image [02036]embedded image 1-207 CF.sub.3 [02037]embedded image [02038]embedded image (500 MHz, Chloroform-d) δ 7.50-7.43 (m, 2H), 7.35 (s, 1H), 7.11-7.03 (m, 2H), 4.07 (q, J = 8.0 Hz, 2H), 3.95 (t, J = 7.5 Hz, 2H), 2.48 (t, J = 7.0 Hz, 2H), 2.11-2.00 (m, 2H), 1.17 (t, J = 8.0 Hz, 3H). 1-208 CF.sub.3 [02039]embedded image [02040]embedded image (500 MHz, Chloroform-d) δ 7.45-7.32 (m, 3H), 7.26- 7.14 (m, 4H), 6.83-6.76 (m, 2H). 1-209 CF.sub.3 [02041]embedded image [02042]embedded image (500 MHz, Chloroform-d) δ 7.53-7.45 (m, 3H), 7.44- 7.27 (m, 3H), 7.11-7.03 (m, 4H), 4.98 (s, 2H). 1-210 CF.sub.3 [02043]embedded image [02044]embedded image (500 MHz, Chloroform-d) δ 7.44-7.27 (m, 4H), 7.13- 7.07 (m, 5H), 4.98 (s, 2H). 1-211 CF.sub.3 [02045]embedded image [02046]embedded image (500 MHz, Chloroform-d) δ 7.50-7.42 (m, 3H), 7.35 (s, 1H), 7.14-7.03 (m, 3H), 5.12 (s, 2H), 3.86 (s, 3H). 1-212 CF.sub.3 [02047]embedded image [02048]embedded image (500 MHz, Chloroform-d) δ 8.07-8.00 (m, 3H), 7.64- 7.56 (m, 3H), 7.54-7.42 (m, 2H),7.31 (s, 1H), 7.11-7.03 (m, 2H), 5.70 (s, 2H). 1-213 CF.sub.3 [02049]embedded image [02050]embedded image (500 MHz, Chloroform-d) δ 8.03-7.89 (m, 2H), 7.64- 7.56 (m, 2H), 7.54-7.34 (m, 1H), 7.28-7.18 (m, 3H), 5.70 (s, 2H). 1-214 CF.sub.3 [02051]embedded image [02052]embedded image (500 MHz, Chloroform-d) δ 7.42 (d, J = 7.0 Hz, 2H), 7.22 (d, J = 7.0 Hz, 2H), 7.12 (s, 1H), 2.47 (s, 6H), 2.33 (s, 3H). 1-215 CF.sub.3 [02053]embedded image [02054]embedded image (500 MHz, Chloroform-d) δ 7.47 (d, J = 7.5 Hz, 2H), 7.39 (d, J = 7.5 Hz, 2H), 7.12 (s, 1H), 2.59 (q, J = 8.0 Hz, 4H), 1.04 (t, J = 8.0 Hz, 6H). 1-216 CF [02055]embedded image [02056]embedded image 1-217 CF.sub.3 [02057]embedded image [02058]embedded image 1-218 CH.sub.2F [02059]embedded image [02060]embedded image 1-219 CH.sub.2F [02061]embedded image [02062]embedded image 1-220 CH.sub.2F [02063]embedded image [02064]embedded image 1-221 CHF.sub.2 [02065]embedded image [02066]embedded image 1-222 CHF.sub.2 [02067]embedded image [02068]embedded image 1-223 CFCF.sub.3 [02069]embedded image [02070]embedded image 1-224 CFCF.sub.3 [02071]embedded image [02072]embedded image 1-225 CFCF.sub.3 [02073]embedded image [02074]embedded image 1-226 CF.sub.3 [02075]embedded image [02076]embedded image 1-227 CF.sub.3 [02077]embedded image [02078]embedded image 1-228 CF.sub.3 [02079]embedded image [02080]embedded image 1-229 CF.sub.3 [02081]embedded image [02082]embedded image 1-230 CF.sub.3 [02083]embedded image [02084]embedded image 1-231 CF.sub.3 [02085]embedded image [02086]embedded image 1-232 CF.sub.3 [02087]embedded image [02088]embedded image 1-233 CF.sub.3 [02089]embedded image [02090]embedded image 1-234 CF.sub.3 [02091]embedded image [02092]embedded image 1-235 CF.sub.3 [02093]embedded image [02094]embedded image 1-236 CF.sub.3 [02095]embedded image [02096]embedded image 1-237 CF.sub.3 [02097]embedded image [02098]embedded image 1-238 CF.sub.3 [02099]embedded image [02100]embedded image 1-239 CF.sub.3 [02101]embedded image [02102]embedded image 1-240 CF.sub.3 [02103]embedded image [02104]embedded image .sup.1H NMR (500 MHz, Chloroform-d) 7.56-7.48 (m, 2H), 7.41-7.33 (m, 3H), 7.00- 6.91 (m, 2H), 5.27 (hept, J = 6.5 Hz, 1H), 1.73 (d, J = 7.0 Hz, 3H), 1.31 (d,J = 6.5 Hz, 6H). 1-241 CF.sub.3 CN [02105]embedded image 1-242 CF.sub.3 [02106]embedded image [02107]embedded image .sup.1H NMR (500MHz, Chloroform-d) δ 7.77-7.66 (m, 4H), 7.60-7.53 (m, 2H), 7.41-7.22 (m, 3H). 1-243 CF.sub.3 [02108]embedded image [02109]embedded image .sup.1H NMR (500MHz, Chloroform-d) δ 7.51-7.44 (m, 2H), 7.42-7.33 (m, 4H), 7.20 (s, 1H), 7.07-7.00 (m, 3H). 1-244 CF.sub.3 [02110]embedded image [02111]embedded image .sup.1H NMR (500MHz, Chloroform-d) δ 7.59-7.51 (m, 2H), 7.41-7.33 (m, 2H), 7.15 (s, 1H), 2.59 (s, 3H), 2.51 (s, 3H), 2.30 (s, 3H). 1-245 CF.sub.3 [02112]embedded image [02113]embedded image .sup.1H NMR (500 MHz, Chloroform-d) δ 7.55-7.47 (m, 2H), 7.41-7.30 (m, 2H), 7.11 (s, 1H), 2.47 (s, 6H), 2.32 (s, 3H). 1-246 CF.sub.3 [02114]embedded image [02115]embedded image .sup.1H NMR (500 MHz, Chloroform-d) 7.58-7.42 (m, 3H), 7.31-7.12(m, 3H), 2.85 (t, J = 7.5 Hz, 2H), 1.38-1.26 (m, 12H), 0.89 (t, J = 7.0 Hz, 1H). 1-247 CF.sub.3 [02116]embedded image [02117]embedded image .sup.1H NMR (500 MHz, Chloroform-d) 7.65-7.49 (m, 6H), 7.42-7.27 (m, 4H), 7.11 (s, 1H), 4.98 (s, 2H). 1-248 CF.sub.3 [02118]embedded image [02119]embedded image 1-249 CF.sub.3 [02120]embedded image [02121]embedded image 1-250 CF.sub.3 [02122]embedded image [02123]embedded image 1-251 CF.sub.3 [02124]embedded image Me

    [0190] The method for preparing the compound of the invention will be explained in detail in the following program and embodiment. The material is commercial available or prepared through known method reported in the literature or shown in the route. Those skilled in the art should understand that the compound of the invention can also be synthesized by other synthetic route. Although the detailed material and reaction condition in the synthetic route have been explicated in the following text, it is still easy to be replaced by other similar material and condition. Isomer of the compound, for example, that produced with the variation of the preparation method of the present invention is included in the scope of the present invention. In addition, the following preparation method can be further modified according to the disclosures of the present invention by using common chemical method known to those skilled in the art, for example, protection of suitable group in the process of the reaction, etc.

    [0191] The following method of application can be used to improve further understanding of the preparation method of the present invention. The specific material, class and condition have been determined to be further explication of the present invention, not to be any limit of the reasonable scope thereof. Reagents of the following synthetic compound showed in the table can either be purchased from the market or easily prepared by those skilled in the art.

    [0192] Examples of representative compounds are as follows:

    [0193] 1. Synthesis of Compound 1

    ##STR02125##

    [0194] (1) experimental apparatus: a 50 mL round bottom single-necked flask, a magnetic stirrer, and a thermostatic magnetic stirrer.

    [0195] Compound II (1 g, 3.9 mmol), Compound 1-a (0.72 g, 5.9 mmol), and potassium carbonate (1.62 g, 11.7 mmol) were placed in the round bottom flask, added with 1,4-dioxane (10 mL)/water (2 mL) and then subjected to replacement of nitrogen gas three times, followed by the quickly addition of Pd(dppf)Cl.sub.2CH.sub.2Cl.sub.2 (0.16 g), and subjected to replacement of nitrogen gas three times, then the reaction solution was subjected to replacement of nitrogen gas three times once again, and finally the reaction was carried out at 100° C. for 36 hours. The reaction was complete detected by HPLC, the reaction system was concentrated, and separated by column chromatography to give 0.8 g (3.1 mmol, yield: 79%) of Compound 1-b (white solid).

    [0196] (2) experimental apparatus: 50 mL round bottom single-necked flask, magnetic stirrer, thermostatic magnetic stirrer, and spherical condenser.

    [0197] Compound 1-b (0.8 g, 3.1 mmol) was placed in the round bottom flask, 8 mL of water and sodium hydroxide (0.37 g, 9.3 mmol) were added, the resulting mixture was reacted at 80° C. for 12 h. After the reaction was completed, the reaction solution was extracted with 30 mL of dichloromethane three times. The aqueous phase was adjusted to pH 2 with 1N HCl solution, and a white solid was precipitated. The filter cake was obtained by filtration, and then dried to give 0.65 g (2.7 mmol, yield 87%) of Compound 1.

    [0198] 2. Synthesis of Compound 27

    ##STR02126##

    [0199] (1) Compound II (1 g, 3.9 mmol), Compound 27-a (0.92 g, 5.9 mmol), and potassium carbonate (1.62 g, 11.7 mmol) were placed in a round bottom flask, added with 1,4-dioxane (10 mL)/water (2 mL) and then subjected to replacement of nitrogen gas three times, followed by the quickly addition of Pd(dppf) Cl.sub.2CH.sub.2Cl.sub.2 (0.16 g) and subjected to replacement of nitrogen gas three times, the reaction solution was then subjected to replacement of nitrogen gas three times once again, and finally the reaction was carried out at 120° C. for 36 hours. The reaction was complete detected by HPLC, the reaction system was concentrated and purified by concentration column chromatography (PE:EA=5:1) to give 0.71 g (2.4 mmol, yield 61%) of Compound 27-b (white solid).

    [0200] (2) Compound 27-b (0.71 g, 2.4 mmol) was placed in a round bottom flask, 8 mL of water and sodium hydroxide (0.096 g, 2.4 mmol) were added, the resulting mixture was reacted at 120° C. for 12 h. The reaction was complete detected by TEC, then the reaction solution was cooled and extracted three times with 30 mL of dichloromethane. The aqueous phase was adjusted to pH=2 with 1N HCl solution, and a white solid was precipitated, which was filtered to give a filter cake, and dried to give 0.35 g (1.3 mmol, yield 87%) of Compound 27.

    [0201] 3. Synthesis of Compound 32

    ##STR02127##

    [0202] (1) Compound II (1 g, 3.9 mmol), Compound 32-a (0.82 g, 5.9 mmol), and potassium carbonate (1.62 g, 11.7 mmol) were placed in a round bottom flask, added with 1,4-dioxane (10 mL)/water (1 mL) and then subjected to replacement of nitrogen gas three times, followed by the quickly addition of Pd(dppf)Cl.sub.2CH.sub.2Cl.sub.2 (0.16 g), and subjected to replacement of nitrogen gas three times, the reaction solution was then subjected to replacement of nitrogen gas three times once again, and finally the reaction was carried out 110° C. for 36 hours. After the reaction was complete detected by HPLC, the reaction solution was concentrated and purified by column chromatography (PE:EA=5:1) to give 0.8 g (3.1 mmol, yield 79%) of Compound 32-b (white solid).

    [0203] (2) Compound 32-b (0.8 g, 3.1 mmol) was placed in a round bottom flask, added with 8 mL of water and sodium hydroxide (0.37 g, 9.3 mmol), and then reacted at 120° C. for 12 h. After the reaction was complete detected by TLC, the reaction solution was extracted three times with 30 mL of dichloromethane. The aqueous phase was adjusted to pH 2 with 1N HCl solution, and a white solid was precipitated, which was filtered to give a filter cake, and dried to give 0.65 g (2.7 mmol, yield 87%) of Compound 32.

    [0204] 4. Synthesis of Compound 207

    ##STR02128##

    [0205] (1) Compound II (1 g, 3.9 mmol), Compound 207-a (0.83 g, 5.9 mmol), and potassium carbonate (1.61 g, 11.7 mmol) were placed in a round bottom flask, added with 1,4-dioxane (10 mL)/water (1 mL) and then subjected to replacement of nitrogen gas three times, followed by the quickly addition of Pd(dppf)Cl.sub.2CH.sub.2Cl.sub.2 (0.16 g), and then subjected to replacement of nitrogen gas three times, the reaction solution was then subjected to replacement of nitrogen gas three times once again, and finally the reaction was carried out at 110° C. for 36 hours. After the reaction was complete detected by HPLC, the reaction solution was concentrated and purified by column chromatography (PE:EA=3:1) to give 0.57 g (2.1 mmol, yield 53%) of Compound 207-b (white solid).

    [0206] (2) Compound 207-b (0.57 g, 2.1 mmol) was placed in a round bottom flask, added with 6 mL of HBr (30%, AcOH) and reacted at 50° C. for 12 h. After the reaction was complete detected by HPLC, the reaction solution was cooled to room temperature, added with water to precipitate, and filtered to obtain a white solid, which was dried to give 0.25 g (1.0 mmol, yield 47%) of Compound 207.

    [0207] 5. Synthesis of Compound 211

    ##STR02129##

    [0208] (1) Compound

    ##STR02130##

    (1.0 g, 5.8 mmol, 1.0 eq), bis-boronic acid pinacol ester (1.6 g, 6.38 mmol, 1.1 eq), and potassium acetate (1.1 g, 11.6 mmol, 2.0 eq) were placed in a 100 mL round bottom flask, added with toluene (40 mL) and then subjected to replacement of nitrogen gas once, followed by the quickly addition of Pd(dppf)Cl.sub.2CH.sub.2Cl.sub.2 (237 mg, 0.29 mmol, 0.05 eq), and then subjected to replacement of nitrogen gas three times, and then heated to 120° C. and reacted for 16 h. The system was cooled to room temperature, and Compound II (1.48 g, 5.8 mmol, 1.0 eq), K.sub.2CO.sub.3 (1.6 g, 11.6 mmol, 2.0 eq), 95% ethanol (8 mL) and Pd(dppf)Cl.sub.2CH.sub.2Cl.sub.2 (237 mg, 0.29 mmol, 0.05 eq) were added, and then subjected to replacement of nitrogen gas three times, and heated to 120° C. (reflux) and reacted for 4 h. After the reaction was complete detected by LCMS, the reaction mixture was concentrated and then added with silica gel and purified by column chromatography to give obtain Compound 211-b (560 mg, Y: 36%).

    [0209] (2) Compound 211-b (0.56 g, 2.0 mmol) was placed in a round bottom flask, added with AcOK (0.98 g, 10 mmol) and DMSO (5.6 mL) and then reacted at 125° C. for 3 h. After the reaction was complete, the temperature was lowered. The reaction solution was added with 20 mL of water, extracted three times with 30 mL of dichloromethane, and the aqueous phase was adjusted to pH 6 with 1N HCl solution, and a white solid was precipitated, which was filtered to obtain a filter cake, and dried to give 0.26 g of Compound 211 (1.6 mmol, yield 50%).

    [0210] 6. Synthesis of Compound 733

    ##STR02131##

    [0211] (1) experimental apparatus: a 50 mL round bottom single-necked flask, a magnetic stirrer, and a thermostatic magnetic stirrer.

    [0212] Compound II (1 g, 3.9 mmol), Compound 733-a (0.83 g, 5.9 mmol), and cesium carbonate (3.81 g, 11.7 mmol) were placed in the round bottom flask, added with 1,4-dioxane (20 mL)/water (5 mL) and then subjected to replacement of nitrogen gas three times, followed by the quickly addition of Pd(dppf)Cl.sub.2CH.sub.2Cl.sub.2 (0.16 g), and then subjected to replacement of nitrogen gas three times, and then the reaction solution was subjected to replacement of nitrogen gas three times once again, and finally the reaction was carried out at 100° C. for 36 hours. After the reaction was complete detected by HPLC, the reaction system was concentrated and purified by column chromatography to give 0.6 g (2.2 mmol, yield: 56%) of Compound 733-b (white solid).

    [0213] (2) experimental apparatus: a 50 mL round bottom single-necked flask, a magnetic stirrer, a thermostatic magnetic stirrer, and a spherical condenser.

    [0214] Compound 733-b (0.6 g, 2.2 mmol) was placed in the round bottom flask, added with 8 mL of water and sodium hydroxide (0.26 g, 6.6 mmol) and reacted at 80° C. for 12 h. After the reaction was complete, the reaction solution was extracted three times with 30 mL of dichloromethane, the aqueous phase was adjusted to pH 2 with 1N HCl solution, and a white solid was precipitated, a filter cake was obtained by filtration, and the filter cake was dried to give 0.41 g (1.6 mmol, yield 73%) of Compound 733.

    [0215] 7. Synthesis of Compound 734

    ##STR02132##

    [0216] (1) experimental apparatus: a 50 mL round bottom single-necked flask, a magnetic stirrer, and a thermostatic magnetic stirrer.

    [0217] Compound II (1 g, 3.9 mmol), Compound 734-a (1.0 g, 5.9 mmol), and cesium carbonate (3.81 g, 11.7 mmol) were placed in the round bottom flask, added with 1,4-dioxane (20 mL)/water (5 mL) and then subjected to replacement of nitrogen three times, followed by the quickly addition of Pd(dppf)Cl.sub.2CH.sub.2Cl.sub.2 (0.16 g), and subjected to replacement of nitrogen gas three times, then the reaction solution was subjected to replacement of nitrogen gas three times once again, and finally the reaction was carried out at 110° C. for 36 hours. After the reaction was complete detected by HPLC, the reaction system was concentrated and purified by column chromatography to give 0.7 g (2.3 mmol, yield 57%) of Compound 734-b (white solid).

    [0218] (2) experimental apparatus: a 50 mL round bottom single-necked flask, a magnetic stirrer, a thermostatic magnetic stirrer, and a spherical condenser.

    [0219] Compound 734-b (0.7 g, 2.3 mmol) was placed in the round bottom flask, added with 15 mL of water, sodium hydroxide (0.27 g, 6.9 mmol), and then reacted at 90° C. for 12 h. After the reaction was complete, the reaction solution was extracted three time with 30 mL of dichloromethane, the aqueous phase was adjusted to pH 2 with 1N HCl solution, and a white solid was precipitated, which was filtered to obtain a filter cake, and dried to give 0.41 g (1.6 mmol, yield 73%) of Compound 734.

    [0220] 8. Synthesis of Compound 744

    ##STR02133##

    [0221] (1) Compound II (1 g, 3.9 mmol) was placed in a round bottom flask, added with dioxane: H.sub.2O=3:1 (10 mL), sodium hydroxide (0.23 g, 5.8 mmol), and then reacted at 120° C. for 5 h. After the reaction was complete detected by TLC, the reaction solution was subjected to rotary evaporation to remove the solvent, added with 20 mL of water, and then extracted three times with 20 mL of dichloromethane. The aqueous phase was adjusted to pH 2 with 1N HCl solution, and a white solid was precipitated, which was dried to give 0.6 g (2.5 mmol, yield 65%) of Compound 744-b.

    [0222] (2) Compound 744-b (1 g, 4.1 mmol), Compound 744-a (0.96 g, 6.1 mmol), and potassium carbonate (1.69 g, 12.3 mmol) were placed in a round bottom flask, added with 1,4-dioxane (10 mL)/water (1 mL) and then subjected to replacement of nitrogen gas three times, followed by the quickly addition of Pd(dppf)Cl.sub.2CH.sub.2Cl.sub.2 (0.16 g), and then subjected to replacement of nitrogen gas three times, and then the reaction solution was subjected to replacement of nitrogen gas three times once again, and finally the reaction was carried out at 110° C. for 36 hours. After the reaction was complete detected by HPLC, the reaction mixture was concentrated, then added with 20 mL of water, and extracted three times with 30 mL of dichloromethane. The aqueous phase was adjusted to pH 4 with 1N HCl solution, and a white solid was precipitated, which was filtered to obtain a filter cake, and then dried to give 0.51 g of Compound 744 (1.85 mmol, yield 45%).

    [0223] 9. Synthesis of Compound 770

    ##STR02134##

    [0224] (1) Compound II (1 g, 3.9 mmol), Compound 770-a (0.92 g, 5.9 mmol), and cesium carbonate (3.81 g, 11.7 mmol) were placed in a round bottom flask, added with 1,4-dioxane (10 mL)/water (1 mL) and then subjected to replacement of nitrogen gas three times, followed by the quickly addition of Pd(dppf)Cl.sub.2CH.sub.2Cl.sub.2 (0.16 g) and then subjected to replacement of nitrogen gas three times, then the reaction solution was subjected to replacement of nitrogen gas three times once again, and finally the reaction was carried out at 110° C. for 36 hours. After the reaction was complete detected by HPLC, the reaction solution was directly concentrated and purified by column chromatography (PE:EA=3:1) to give 0.63 g (2.3 mmol, yield 58.9%) of Compound 770-b (white solid).

    [0225] (2) Compound 770-b (0.63 g, 2.3 mmol) was placed in a round bottom flask, added with AcOK (1.12 g, 11.5 mmol) and DMSO (6.3 mL) and reacted at 125° C. for 3 h. After the reaction was complete, the temperature was lowered. The reaction solution was added with 20 mL of water, and extracted three times with 30 mL of dichloromethane. The aqueous phase was adjusted to pH 6 with 1N HCl solution, and a white solid was precipitated, which was filtered to obtain a filter cake, and dried to give 0.41 g of Compound 770 (1.6 mmol, yield 73%).

    [0226] 10. Synthesis of Compound 774

    ##STR02135##

    [0227] (1) Compound II (1 g, 3.9 mmol), Compound 774-a (0.737 g, 5.9 mmol), and potassium carbonate (1.62 g, 11.7 mmol) were placed in a round bottom flask, added with 1,4-dioxane (10 mL)/water (1 mL) and then subjected to replacement of nitrogen gas three times, then followed by the quickly addition of Pd(dppf)Cl.sub.2CH.sub.2Cl.sub.2 (0.16 g), and then subjected to replacement of nitrogen gas three times, then the reaction solution was subjected to replacement of nitrogen gas three times once again, and finally the reaction was carried out at 110° C. for 36 hours. After the reaction was complete detected by HPLC, the reaction solution was concentrated and purified by column chromatography (PE:EA=5:1) to give 0.82 g (3.2 mmol, yield 83%) of Compound 774-b (white solid).

    [0228] (2) Compound 774-b (0.82 g, 3.2 mmol) was placed in a round bottom flask, added with AcOK (1.56 g, 16 mmol) and DMSO (8.3 mL) and reacted at 120° C. for 3 h. After the reaction was complete, the temperature was lowered. The reaction solution was added with 20 mL of water, and extracted with three time with 30 mL of dichloromethane. The aqueous phase was adjusted to pH 4 with 1N HCl solution, and a white solid was precipitated, which was filtered to obtain a filter cake, and then dried to give 0.50 g of Compound 774 (2.08 mmol, Yield 65%).

    [0229] 11. Synthesis of Compound 1-39

    ##STR02136##

    [0230] Compound 32 (1 eq.),

    ##STR02137##

    (1.1 eq.), potassium carbonate (1.5 eq.) and acetonitrile (5 V, V represents per gram of substrate corresponding to 1 mL of acetonitrile, similarly hereinafter) were added at room temperature into a 50 mL single-mouth eggplant-shaped bottle, stirred for 1 h at a controlled temperature of 20° C. After the reaction was complete detected by TLC, the reaction system was subjected to a rotary evaporator to remove acetonitrile, added with with water-ethyl acetate for extraction, the residue was separated by column chromatography with silica gel (100 mesh to 200 mesh) to give the product in a yield of 79%.

    [0231] 12. Synthesis of Compound 1-127

    ##STR02138##

    [0232] Compound 744 (1 eq.),

    ##STR02139##

    (2 eq.), potassium carbonate (3 eq.) and acetonitrile (10 V) were added into a 50 mL single-mouth eggplant-shaped flask at room temperature, and stirred at a controlled temperature of 80° C. for 12 h. After the reaction was complete detected by TLC, the reaction system was subjected to a rotary evaporator to remove acetonitrile, added with water-ethyl acetate for extraction. The residue was separated by column chromatography with silica gel (100 mesh to 200 mesh) to give a product in yield of 83%.

    [0233] 13. Synthesis of Compound 1-170

    ##STR02140##

    [0234] Referring to the synthesis method of Compound 1, Compound 4 was prepared, and then Compound 4-1 was prepared according to the synthesis method disclosed in WO2012142162A2. Finally, Compound 4-1 (1 eq.).),

    ##STR02141##

    (1.1 eq.), potassium carbonate (3 eq.) and acetonitrile (10 V) were added into a 50 mL single-mouth eggplant-shaped bottle at room temperature, hearted to 80° C., and stirred for 12 h. After the reaction was complete detected by TLC, the reaction system was subjected to a rotary evaporator to remove acetonitrile, and the residue was separated by column chromatography with silica gel (100 mesh to 200 mesh) to give a product in yield of 68%.

    [0235] 14. Synthesis of Compound 1-213

    ##STR02142##

    [0236] Compound 744 (1 eq.),

    ##STR02143##

    (1.5 eq.), triethylamine (3 eq.) and dichloromethane (10 V) were added into a 50 mL single-mouth eggplant-shaped flask at room temperature, and stirred at a controlled temperature of 40° C. for 1 h. After the reaction was complete detected by TLC, the reaction system was subjected to a rotary evaporator to remove dichloromethane, and added with water-ethyl acetate for extraction. The residue was separated by column chromatography with silica gel (100 mesh to 200 mesh) to give a product in yield of 72%.

    [0237] 15. Synthesis of Compound 1-242

    ##STR02144##

    [0238] Compound 1 (1 eq.),

    ##STR02145##

    (1.1 eq.), potassium carbonate (3 eq.) and acetonitrile (10 V) were added into a 50 mL single-mouth eggplant-shaped bottle at room temperature, and stirred at room temperature for 30 min. After the reaction was complete detected by TLC, the reaction system was subjected to distillation under reduced pressure to remove acetonitrile, then added with water (5V) for dissolution and extracted with ethyl acetate (5V*3). The ethyl acetate was removed by evaporation under reduced pressure, and the residue was purified by column chromatography with silica gel (100 mesh to 200 mesh) to give a product as Compound 1-242 in yield of 85%.

    [0239] 16. Synthesis of Compound 1-243

    ##STR02146##

    [0240] Compound 1 (1 eq.), triethylamine (3 eq.) and dichloromethane (5 V) were added into a 50 mL single-mouth eggplant-shaped flask under ice bath, and added dropwise with

    ##STR02147##

    (1.2 eq.) under ice bath, then stirred at room temperature for 30 min. After the reaction was complete detected by TLC, the reaction system was added with water (5V) and extracted with dichloromethane (5V*3). The dichloromethane was removed by distillation under reduced pressure, and the residue was separated by column chromatography with silica gel (100 mesh to 200 mesh) to give a product as Compound 1-243 in yield of 78%.

    [0241] 17. Synthesis of Compound 1-244

    ##STR02148##

    [0242] Compound 1 (1 equivalent), Phenofluor (1.5 equivalent), cesium fluoride (3 equivalents), and toluene (10 V) were added into a 50 mL single-mouth eggplant-shaped bottle at room temperature, heated to 80° C. and stirred for 18 h. After the reaction was complete detected by TLC, intermediate Compound 1-244-a was obtained after workup. Compound 1-244-a (1 eq.),

    ##STR02149##

    (1.2 eq.), potassium carbonate (3 eq.) and acetonitrile (10 V) were added to another 50 mL single-mouth eggplant-shaped bottle, heated to 80° C. and stirred for 18 h. After the reaction was complete detected by TLC, the reaction system was subjected to evaporation under reduced pressure to remove acetonitrile, then added with water (5V) for dissolution and extracted with ethyl acetate (5V*3). The ethyl acetate was removed by evaporation under reduced pressure, and the residue was purified by column chromatography with silica gel (100 mesh to 200 mesh) to give a product as Compound 1-244 in yield of 69%.

    [0243] 18. Synthesis of Compound 1-245

    ##STR02150##

    [0244] Compound 1 (1 eq.), POCl.sub.3 (1.5 eq.), 1,2-dichloroethane (10 V), and 5% N,N— dimethylformamide were added into a 50 mL single-mouth eggplant-shaped bottle at room temperature, heated to 80° C. and stirred for 6 h. After the reaction was complete detected by TLC, water (5V) was added for dissolution, and then extraction was carried out with 1,2-dichloroethane (5V*3). The 1,2-dichloroethane was removed by distillation under reduced pressure to give Compound 1-245-a. Compound 1-245-a (1 eq.),

    ##STR02151##

    (1.2 eq.), potassium hydroxide (3 eq.) and N,N-dimethylformamide (10 V) were added at room temperature into another 50 mL single-mouth eggplant-shaped bottle, heated to 100° C., and stirred for 18 h. After the reaction was complete detected by TLC, water (5 V) was added for dissolution, and then extraction was carried out with ethyl acetate (5 V*3). The ethyl acetate was removed by distillation under reduced pressure, and the residue was separated by column chromatography with silica gel (100 mesh to 200 mesh) to give a product as Compound 1-245 in a yield of 52%.

    [0245] The compounds in Table 1 and Table 2 are prepared by the methods described above.

    [0246] Evaluation of Biological Activity:

    [0247] The activity level standard of harmful plant destruction (i.e. growth inhibition rate) is as follows:

    [0248] Level 10: completely dead;

    [0249] Level 9: above 90% growth inhibition rate;

    [0250] Level 8: above 80% growth inhibition rate;

    [0251] Level 7: above 70% growth inhibition rate;

    [0252] Level 6: above 60% growth inhibition rate;

    [0253] Level 5: above 50% growth inhibition rate;

    [0254] Level 4: above 40% growth inhibition rate;

    [0255] Level 3: above 30% growth inhibition rate;

    [0256] Level 2: above 20% growth inhibition rate;

    [0257] Level 1: below 20% growth inhibition rate;

    [0258] Level 0: no effect.

    [0259] The above described growth inhibition rates are fresh weight inhibition rates.

    [0260] Experiment of post-emergence test: monocotyledonous and dicotyledonous weed seeds as well as main crop seeds (i.e., wheat, corn, rice, soybean, cotton, oilseed rape, millet and sorghum) were put into a plastic pot loaded with soil, then covered with 0.5-2 cm of soil, and the seeds were allowed to grow in good greenhouse environment. The test plants were treated at 2-3 leaf stage 2-3 weeks after sowing. The test compounds of the invention were dissolved in acetone respectively, then added with Tween-80 and diluted by a certain amount of water to give solutions with certain concentrations, and added with 80% vegetable oil methyl ester synergist at 1500 g/ha. The solution was sprayed to the plants with a sprayer. The plants were cultured for 3 weeks in the greenhouse. The experiment results of weed controlling effect after 3 weeks were listed in Table 3 and Table 4.

    TABLE-US-00003 TABLE 3 Experiment on weed control effect of compounds of Formula I in Post-emergence stage Compound Amaranthus Rorippa Veronica Chenopo- No. retroflexus indica polita diaceae Dose 1 10 10 10 8 2000 g/ha 4 10 10 10 8 2000 g/ha 8 10 10 10 8 2000 g/ha 24 10 10 10 10 2000 g/ha 26 10 10 10 10 1000 g/ha 27 10 10 10 10 1000 g/ha 28 10 10 10 10 1000 g/ha 29 10 10 10 10 1000 g/ha 30 10 10 10 10 1000 g/ha 31 10 10 10 10 1000 g/ha 32 10 10 10 10 1000 g/ha 33 10 10 10 10 1000 g/ha 34 10 10 10 10 1000 g/ha 35 10 10 10 10 1000 g/ha 36 10 10 10 10 1000 g/ha 37 10 10 10 10 1000 g/ha 38 10 10 10 10 1000 g/ha 39 10 10 10 10 1000 g/ha 40 10 10 10 10 1000 g/ha 41 10 10 10 10 1000 g/ha 42 10 10 10 10 1000 g/ha 43 10 10 10 10 1000 g/ha 44 10 10 10 10 1000 g/ha 45 10 10 10 10 1000 g/ha 46 10 10 10 10 1000 g/ha 47 10 10 10 10 1000 g/ha 48 10 10 10 10 1000 g/ha 49 10 10 10 10 1000 g/ha 50 10 10 10 10 1000 g/ha 51 10 10 10 10 1000 g/ha 52 10 10 10 10 1000 g/ha 53 10 10 10 10 1000 g/ha 54 10 10 10 10 1000 g/ha 55 10 10 10 10 1000 g/ha 56 10 10 10 10 1000 g/ha 57 10 10 10 10 1000 g/ha 58 10 10 10 10 1000 g/ha 59 10 10 10 10 1000 g/ha 60 10 10 10 10 1000 g/ha 61 10 10 10 10 1000 g/ha 62 10 10 10 10 1000 g/ha 63 10 10 10 10 1000 g/ha 64 10 10 10 10 1000 g/ha 65 10 10 10 10 1000 g/ha 66 10 10 10 10 1000 g/ha 67 10 10 10 10 1000 g/ha 68 10 10 10 10 1000 g/ha 69 10 10 10 10 1000 g/ha 70 10 10 10 10 1000 g/ha 71 10 10 10 10 1000 g/ha 72 10 10 10 10 1000 g/ha 77 10 10 10 10 2000 g/ha 81 10 10 10 10 1000 g/ha 82 10 10 10 10 1000 g/ha 83 10 10 10 10 1000 g/ha 92 10 10 10 10 1000 g/ha 93 10 10 10 10 1000 g/ha 94 10 10 10 10 1000 g/ha 95 10 10 10 10 1000 g/ha 96 10 10 10 10 1000 g/ha 97 10 10 10 10 1000 g/ha 111 10 10 10 10 1000 g/ha 114 10 10 10 10 1000 g/ha 128 10 10 10 10 1000 g/ha 163 10 10 10 10 2000 g/ha 165 10 10 10 10 2000 g/ha 166 10 10 10 10 2000 g/ha 168 10 10 10 10 2000 g/ha 169 10 10 10 10 2000 g/ha 173 10 10 10 10 2000 g/ha 179 10 10 10 10 2000 g/ha 202 10 10 10 10 2000 g/ha 204 10 10 10 10 2000 g/ha 205 10 10 10 10 2000 g/ha 206 10 10 10 10 2000 g/ha 207 10 10 10 10 2000 g/ha 211 10 10 10 10 2000 g/ha 212 10 10 10 10 2000 g/ha 214 10 10 10 10 2000 g/ha 218 10 10 10 10 2000 g/ha 219 10 10 10 10 2000 g/ha 220 10 10 10 10 2000 g/ha 221 10 10 10 10 2000 g/ha 222 10 10 10 10 2000 g/ha 223 10 10 10 10 2000 g/ha 224 10 10 10 10 2000 g/ha 225 10 10 10 10 2000 g/ha 226 10 10 10 10 2000 g/ha 227 10 10 10 10 2000 g/ha 231 10 10 10 10 2000 g/ha 236 10 10 10 10 2000 g/ha 263 10 10 10 10 2000 g/ha 279 10 10 10 10 2000 g/ha 323 10 10 10 10 2000 g/ha 349 10 10 10 10 2000 g/ha 370 10 10 10 10 2000 g/ha 371 10 10 10 10 2000 g/ha 380 10 10 10 10 2000 g/ha 414 10 10 10 10 3000 g/ha 418 10 10 10 10 3000 g/ha 439 10 10 10 10 3000 g/ha 540 10 10 10 10 3000 g/ha 543 10 10 10 10 3000 g/ha 544 10 10 10 10 3000 g/ha 546 10 10 10 10 3000 g/ha 570 10 10 10 10 3000 g/ha 588 10 10 10 10 3000 g/ha 589 10 10 10 10 3000 g/ha 594 10 10 10 10 3000 g/ha 595 10 10 10 10 3000 g/ha 597 10 10 10 10 3000 g/ha 613 10 10 10 10 3000 g/ha 634 10 10 10 10 3000 g/ha 636 10 10 10 10 3000 g/ha 637 10 10 10 10 3000 g/ha 714 10 10 10 10 3000 g/ha 723 10 10 10 10 3000 g/ha 732 10 10 10 10 1000 g/ha 733 10 10 10 10 1000 g/ha 734 10 10 10 10 1000 g/ha 735 10 10 10 10 1000 g/ha 736 10 10 10 10 1000 g/ha 737 10 10 10 10 3000 g/ha 739 10 10 10 10 3000 g/ha 740 10 10 10 10 3000 g/ha 741 10 10 10 10 3000 g/ha 742 10 10 10 10 3000 g/ha 743 10 10 10 10 3000 g/ha 744 10 10 10 10 3000 g/ha 745 10 10 10 10 3000 g/ha 746 10 10 10 10 3000 g/ha 753 10 10 10 10 3000 g/ha 755 10 10 10 10 3000 g/ha 761 10 10 10 10 3000 g/ha 762 10 10 10 10 3000 g/ha 763 10 10 10 10 3000 g/ha 764 10 10 10 10 3000 g/ha 766 10 10 10 10 3000 g/ha 768 10 10 10 10 3000 g/ha 769 10 10 10 10 3000 g/ha 770 10 10 10 10 3000 g/ha 771 10 10 10 10 3000 g/ha 772 10 10 10 10 3000 g/ha 774 10 10 10 10 3000 g/ha 775 10 10 10 10 3000 g/ha 776 10 10 10 10 3000 g/ha 777 10 10 10 10 3000 g/ha 778 10 10 10 10 3000 g/ha 779 10 10 10 10 3000 g/ha 780 10 10 10 10 3000 g/ha 781 10 10 10 10 3000 g/ha 782 10 10 10 10 3000 g/ha 783 10 10 10 10 3000 g/ha 784 10 10 10 10 3000 g/ha 787 10 10 10 10 3000 g/ha 791 10 10 10 10 3000 g/ha 794 10 10 10 10 3000 g/ha 803 10 10 10 10 3000 g/ha 804 10 10 10 10 3000 g/ha 805 10 10 10 10 3000 g/ha 806 10 10 10 10 3000 g/ha 807 10 10 10 10 3000 g/ha 808 10 10 10 10 3000 g/ha 809 10 10 10 10 3000 g/ha 810 10 10 10 10 3000 g/ha 811 10 10 10 10 3000 g/ha 812 10 10 10 10 3000 g/ha 813 10 10 10 10 3000 g/ha 816 10 10 10 10 3000 g/ha 820 10 10 10 10 3000 g/ha 823 10 10 10 10 3000 g/ha 824 10 10 10 10 3000 g/ha 825 10 10 10 10 3000 g/ha 826 10 10 10 10 3000 g/ha 827 10 10 10 10 3000 g/ha 828 10 10 10 10 3000 g/ha 829 10 10 10 10 3000 g/ha 830 10 10 10 10 3000 g/ha 831 10 10 10 10 3000 g/ha 832 10 10 10 10 3000 g/ha 833 10 10 10 10 3000 g/ha 834 10 10 10 10 3000 g/ha 839 10 10 10 10 3000 g/ha 844 10 10 10 10 2000 g/ha 857 10 10 10 10 3000 g/ha 873 10 10 10 10 3000 g/ha 877 10 10 10 10 3000 g/ha 963 10 10 10 10 3000 g/ha 964 10 10 10 10 3000 g/ha 965 10 10 10 10 3000 g/ha 966 10 10 10 10 3000 g/ha 967 10 10 10 10 3000 g/ha 968 10 10 10 10 3000 g/ha 969 10 10 10 10 3000 g/ha 970 10 10 10 10 3000 g/ha 971 10 10 10 10 3000 g/ha 972 10 10 10 10 3000 g/ha 973 10 10 10 10 3000 g/ha 974 10 10 10 10 3000 g/ha 975 10 10 10 10 3000 g/ha 976 10 10 10 10 3000 g/ha 977 10 10 10 10 3000 g/ha 978 10 10 10 10 3000 g/ha 979 10 10 10 10 3000 g/ha 980 10 10 10 10 3000 g/ha 983 10 10 10 10 3000 g/ha 984 10 10 10 10 3000 g/ha 986 10 10 10 10 3000 g/ha 987 10 10 10 10 3000 g/ha 988 10 10 10 10 3000 g/ha 989 10 10 10 10 3000 g/ha 990 10 10 10 10 3000 g/ha 991 10 10 10 10 3000 g/ha 992 10 10 10 10 3000 g/ha 993 10 10 10 10 3000 g/ha 994 10 10 10 10 3000 g/ha 995 10 10 10 10 3000 g/ha 996 10 10 10 10 3000 g/ha 997 10 10 10 10 3000 g/ha 998 10 10 10 10 3000 g/ha 999 10 10 10 10 3000 g/ha 1000 10 10 10 10 3000 g/ha 1001 10 10 10 10 3000 g/ha 1002 10 10 10 10 3000 g/ha 1003 10 10 10 10 3000 g/ha 1004 10 10 10 10 3000 g/ha 1005 10 10 10 10 3000 g/ha 1006 10 10 10 10 3000 g/ha 1007 10 10 10 10 3000 g/ha 1008 10 10 10 10 3000 g/ha 1018 10 10 10 10 3000 g/ha 1076 10 10 10 10 3000 g/ha 1081 10 10 10 10 3000 g/ha 1286 10 10 10 10 3000 g/ha 1522 10 N N 10 3000 g/ha 1523 10 10 10 10 3000 g/ha 1524 10 10 10 10 3000 g/ha Note: N means no data.

    TABLE-US-00004 TABLE 4 Experiment on weed control effect of derivatives of Formula I-1 in Post-emergence stage Compound Amaranthus Rorippa Veronica Chenopo- No. retroflexus indica polita diaceae Dose 1-1 10 10 10 10 3000 g/ha 1-2 10 10 10 10 3000 g/ha 1-3 10 10 10 10 3000 g/ha 1-4 10 10 10 10 3000 g/ha 1-7 10 10 10 10 3000 g/ha 1-8 10 10 10 10 3000 g/ha 1-9 10 10 10 10 3000 g/ha 1-10 10 10 10 10 3000 g/ha 1-14 10 10 10 10 3000 g/ha 1-15 10 10 10 10 3000 g/ha 1-16 10 10 10 10 3000 g/ha 1-17 10 10 10 10 3000 g/ha 1-18 10 10 10 10 3000 g/ha 1-19 10 10 10 10 3000 g/ha 1-22 10 10 10 10 3000 g/ha 1-23 10 10 10 10 3000 g/ha 1-25 10 10 10 10 3000 g/ha 1-26 10 10 10 10 3000 g/ha 1-29 10 10 10 10 3000 g/ha 1-30 10 10 10 10 3000 g/ha 1-31 10 10 10 10 3000 g/ha 1-33 10 10 10 10 3000 g/ha 1-35 10 10 10 10 3000 g/ha 1-36 10 10 10 10 3000 g/ha 1-38 10 10 10 10 3000 g/ha 1-39 10 10 10 10 3000 g/ha 1-40 10 10 10 10 3000 g/ha 1-42 10 10 10 10 3000 g/ha 1-43 10 10 10 10 3000 g/ha 1-47 10 10 10 10 3000 g/ha 1-51 10 10 10 10 3000 g/ha 1-53 10 10 10 10 3000 g/ha 1-54 10 10 10 10 3000 g/ha 1-55 10 10 10 10 3000 g/ha 1-58 10 10 10 10 3000 g/ha 1-60 10 10 10 10 3000 g/ha 1-63 10 10 10 10 3000 g/ha 1-64 10 10 10 10 3000 g/ha 1-65 10 10 10 10 3000 g/ha 1-66 10 10 10 10 3000 g/ha 1-67 10 10 10 10 3000 g/ha 1-68 10 10 10 10 3000 g/ha 1-69 10 10 10 10 3000 g/ha 1-70 10 10 10 10 3000 g/ha 1-71 10 10 10 10 3000 g/ha 1-75 10 10 10 10 3000 g/ha 1-76 10 10 10 10 3000 g/ha 1-77 10 10 10 10 3000 g/ha 1-78 10 10 10 10 3000 g/ha 1-79 10 10 10 10 3000 g/ha 1-80 10 10 10 10 3000 g/ha 1-82 10 10 10 10 3000 g/ha 1-83 10 10 10 10 3000 g/ha 1-84 10 10 10 10 3000 g/ha 1-85 10 10 10 10 3000 g/ha 1-86 10 10 10 10 3000 g/ha 1-87 10 10 10 10 3000 g/ha 1-88 10 10 10 10 3000 g/ha 1-90 10 10 10 10 3000 g/ha 1-91 10 10 10 10 3000 g/ha 1-93 10 10 10 10 3000 g/ha 1-94 10 10 10 10 3000 g/ha 1-95 10 10 10 10 3000 g/ha 1-96 10 10 10 10 3000 g/ha 1-97 10 10 10 10 3000 g/ha 1-98 10 10 10 10 3000 g/ha 1-99 10 10 10 10 3000 g/ha 1-100 10 10 10 10 3000 g/ha 1-101 10 10 10 10 3000 g/ha 1-102 10 10 10 10 3000 g/ha 1-103 10 10 10 10 3000 g/ha 1-104 10 10 10 10 3000 g/ha 1-105 10 10 10 10 3000 g/ha 1-106 10 10 10 10 3000 g/ha 1-107 10 10 10 10 3000 g/ha 1-108 10 10 10 10 3000 g/ha 1-109 10 10 10 10 3000 g/ha 1-110 10 10 10 10 3000 g/ha 1-111 10 10 10 10 3000 g/ha 1-112 10 10 10 10 3000 g/ha 1-113 10 10 10 10 3000 g/ha 1-114 10 10 10 10 3000 g/ha 1-115 10 10 10 10 3000 g/ha 1-116 10 10 10 10 3000 g/ha 1-117 10 10 10 10 3000 g/ha 1-118 10 10 10 10 3000 g/ha 1-119 10 10 10 10 3000 g/ha 1-120 10 10 10 10 3000 g/ha 1-121 10 10 10 10 3000 g/ha 1-122 10 10 10 10 3000 g/ha 1-123 10 10 10 10 3000 g/ha 1-124 10 10 10 10 3000 g/ha 1-125 10 10 10 10 3000 g/ha 1-126 10 10 10 10 3000 g/ha 1-127 10 10 10 10 3000 g/ha 1-128 10 10 10 10 3000 g/ha 1-129 10 10 10 10 3000 g/ha 1-130 10 10 10 10 3000 g/ha 1-131 10 10 10 10 3000 g/ha 1-132 10 10 10 10 3000 g/ha 1-133 10 10 10 10 3000 g/ha 1-134 10 10 10 10 3000 g/ha 1-135 10 10 10 10 3000 g/ha 1-136 10 10 10 10 3000 g/ha 1-137 10 10 10 10 3000 g/ha 1-138 10 10 10 10 3000 g/ha 1-139 10 10 10 10 3000 g/ha 1-140 10 10 10 10 3000 g/ha 1-141 10 10 10 10 3000 g/ha 1-142 10 10 10 10 3000 g/ha 1-143 10 10 10 10 3000 g/ha 1-144 10 10 10 10 3000 g/ha 1-145 10 10 10 10 3000 g/ha 1-146 10 10 10 10 3000 g/ha 1-147 10 10 10 10 3000 g/ha 1-148 10 10 10 10 3000 g/ha 1-149 10 10 10 10 3000 g/ha 1-150 10 10 10 10 3000 g/ha 1-151 10 10 10 10 3000 g/ha 1-152 10 10 10 10 3000 g/ha 1-153 10 10 10 10 3000 g/ha 1-154 10 10 10 10 3000 g/ha 1-155 10 10 10 10 3000 g/ha 1-156 10 10 10 10 3000 g/ha 1-157 10 10 10 10 3000 g/ha 1-158 10 10 10 10 3000 g/ha 1-159 10 10 10 10 3000 g/ha 1-160 10 10 10 10 3000 g/ha 1-162 10 10 10 10 3000 g/ha 1-163 10 10 10 10 3000 g/ha 1-164 10 10 10 10 3000 g/ha 1-165 10 10 10 10 3000 g/ha 1-166 10 10 10 10 3000 g/ha 1-167 10 10 10 10 3000 g/ha 1-169 10 10 10 10 3000 g/ha 1-170 10 10 10 10 3000 g/ha 1-171 10 10 10 10 3000 g/ha 1-172 10 10 10 10 3000 g/ha 1-173 10 10 10 10 3000 g/ha 1-174 10 10 10 10 3000 g/ha 1-175 10 10 10 10 3000 g/ha 1-176 10 10 10 10 3000 g/ha 1-178 10 10 10 10 3000 g/ha 1-179 10 10 10 10 3000 g/ha 1-180 10 10 10 10 3000 g/ha 1-181 10 10 10 10 3000 g/ha 1-207 10 10 10 10 3000 g/ha 1-208 10 10 10 10 3000 g/ha 1-209 10 10 10 10 3000 g/ha 1-210 10 10 10 10 3000 g/ha 1-211 10 10 10 10 3000 g/ha 1-212 10 10 10 10 3000 g/ha 1-213 10 10 10 10 3000 g/ha 1-240 10 10 10 10 3000 g/ha

    Comparative Experiment

    [0261] The post-emergence test conditions were the same as above, and the results are shown in Table 5.

    [0262] Control Compound A:

    ##STR02152##

    [0263] Control Compound B:

    ##STR02153##

    [0264] Control Compound C:

    ##STR02154##

    (from patent CN106316962A)

    [0265] Control Compound D:

    ##STR02155##

    [0266] Control Compound E:

    ##STR02156##

    TABLE-US-00005 TABLE 5 Results of comparison experiment Echinochloa Setaria Rorippa Galium Veronica Compound crus-galli viridis Chenopodiaceae indica aparine polita Dose 32 10 10 10 10 10 10 300 g/ha 35 10 10 10 10 9 10 300 g/ha 51 6 9 10 10 8 9 300 g/ha 202 7 10 10 10 10 8 300 g/ha 206 10 10 10 10 10 10 300 g/ha 207 10 10 10 10 10 10 300 g/ha 220 10 10 10 10 10 10 300 g/ha 733 10 10 10 10 10 10 300 g/ha 739 10 10 10 10 8 10 300 g/ha 740 10 10 10 10 10 10 300 g/ha 744 10 10 10 10 10 10 300 g/ha 779 10 10 10 10 10 10 300 g/ha 844 10 10 10 10 10 10 150 g/ha 1000 10 10 10 10 10 10 300 g/ha 1524 N 10 10 10 9 9 300 g/ha 1-39 10 10 10 10 10 10 150 g/ha 1-43 10 10 10 10 10 10 150 g/ha 1-55 10 10 10 10 10 10 150 g/ha 1-82 7 10 10 10 7 8 150 g/ha 1-86 10 10 10 10 10 10 150 g/ha A 0 3 5 2 5 3 300 g/ha B 0 3 3 3 4 3 300 g/ha C 0 0 3 3 2 2 300 g/ha D 0 0 1 1 0 0 300 g/ha E 0 0 1 1 0 0 300 g/ha Note: N means no data.

    [0267] It can be seen from the above table, the compounds of the present invention have superior herbicidal activity compared with the control compounds.

    [0268] In addition, after testing, the compounds of the present invention have good selectivity for crops when being applied preemergence or postemergence, especially for wheat, rice, soybean, cotton, corn, sorghum, millet and other crops.

    [0269] Experiment of Pre-Emergence Test:

    [0270] Seeds of monocotyledonous and dicotyledonous weeds and main crops (e.g. wheat, corn, rice, soybean, cotton, oilseed rape, millet and sorghum) were put into a plastic pot loaded with soil and covered with 0.5-2 cm of soil. The test compounds of the present invention was dissolved with acetone, then added with Tween-80, diluted by a certain amount of water to reach a certain concentration, and sprayed immediately after sowing. The obtained seeds were incubated for 4 weeks in the greenhouse after spraying. The test results were observed 3 weeks later. It was observed that the herbicides of the present invention mostly had excellent effect at dose of 250 g/ha, especially to weeds such as Echinochloa crusgalli, Digitaria sanguinalis and Abutilon theophrasti, etc., and many compounds had good selectivity for corn, wheat, rice, soybean, oilseed rape, etc.

    [0271] It is found in the experiment that the compounds of the present invention generally have good weed control efficacy, especially for major broadleaf weeds such as Abutilon theophrasti and Bidens bipinnata, etc., which are widely occurred in corn, rice and wheat fields, and have excellent commercial value. Above all, it is noted that the compound of the invention have extremely high activity to broadleaf weeds, which are resistant to ALS inhibitor, like corn gromwell, cleavers and chickweed, etc.

    [0272] Transplanted rice safety evaluation and weed control effect evaluation in rice field:

    [0273] Rice field soil was loaded into a 1/1,000,000 ha pot. The seeds of Echinochloa crusgalli, Scirpus juncoides, Bidens tripartite and Sagittaria trifolia L. were sowed and gently covered with soil, then left to stand still in greenhouse in the state of 0.5-1 cm of water storage. The tuber of Sagittaria trifolia L. was planted in the next day or 2 days later. It was kept at 3-4 cm of water storage thereafter. The weeds were treated by dripping the WP or SC water diluents prepared according to the common preparation method of the compounds of the present invention with pipette homogeneously to achieve specified effective amount when Echinochloa crusgalli, Scirpus juncoides and Bidens tripartite reached 0.5 leaf stage and Sagittaria trifolia L. reached the time point of primary leaf stage.

    [0274] In addition, the rice field soil that loaded into the 1/1,000,000 ha pot was leveled to keep water storage at 3-4 cm depth. The 3 leaf stage rice (japonica rice) was transplanted at 3 cm of transplanting depth the next day. The compound of the present invention was treated by the same way after 5 days of transplantation.

    [0275] The fertility condition of Echinochloa crusgalli, Scirpus juncoides, Bidens tripartite and Sagittaria trifolia L. 14 days after the treatment of the compound of the invention and the fertility condition of rice 21 days after the treatment of the compound of the invention respectively with the naked eye. Evaluate the weed control effect with 1-10 activity standard level. It has been found that many of the compounds of the present invention have excellent activity and selectivity, especially for Sagittaria trifolia L. and Echinochloa crusgalli.

    [0276] Note: The seeds of Echinochloa crusgalli, Scirpus juncoides, Sagittaria trifolia L. and Bidens tripartite were collected from Heilongjiang Province of China. Tests indicated that the weeds were resistant to common rate of pyrazosulfuron-ethyl.

    [0277] Further, the present invention also relates to a herbicidal composition comprising component (i) (such as the compound of Formula I) and component (ii), and some of the compositions are as follows:

    [0278] 1 (Compound No. as shown in Table 1, similarly hereinafter)+Sulcotrione, 1+Mesotrione, 1+Topramezone, 1+Tembotrione, 1+Bicyclopyrone, 1+Tefuryltrione, 1+Benzobicyclon, 1+Lancotrione, 1+Shuangzuocaotong, 1+Huanbifucaotong, 1+Sanzuohuangcaotong, 1+Benzuofucaotong, 1+Pyrasulfotole, 1+Pyrazolate, 1+Benzofenap, 1+Tolpyralate, 1+Fenquinotrione, 1+Isoxaflutole, 1+Fluroxypyr or esters thereof, 1+Halauxifen-methyl, 1+Florpyrauxifen-benzyl, 1+Quinclorac, 1+Quinmerac, 1+Chipton or salts/esters thereof, 1+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 1+MCPB or salts/esters thereof, 1+2,4-D or salts/esters thereof, 1+Dichlorprop or salts/esters thereof, 1+2,4-DB or salts/esters thereof, 1+Dicamba, 1+Picloram, 1+Trichlopyr, 1+Clopyralid, 1+Triclopyr, 1+Flurochloridone, 1+Flurtamone, 1+Diflufenican, 1+Picolinafen, 1+Beflubutamid, 1+Norflurazon, 1+Fluridone.

    [0279] 2+Sulcotrione, 2+Mesotrione, 2+Topramezone, 2+Tembotrione, 2+Bicyclopyrone, 2+Tefuryltrione, 2+Benzobicyclon, 2+Lancotrione, 2+Shuangzuocaotong, 2+Huanbifucaotong, 2+Sanzuohuangcaotong, 2+Benzuofucaotong, 2+Pyrasulfotole, 2+Pyrazolate, 2+Benzofenap, 2+Tolpyralate, 2+Fenquinotrione, 2+Isoxaflutole, 2+Fluroxypyr or esters thereof, 2+Halauxifen-methyl, 2+Florpyrauxifen-benzyl, 2+Quinclorac, 2+Quinmerac, 2+Chipton or salts/esters thereof, 2+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 2+MCPB or salts/esters thereof, 2+2,4-D or salts/esters thereof, 2+Dichlorprop or salts/esters thereof, 2+2,4-DB or salts/esters thereof, 2+Dicamba, 2+Picloram, 2+Trichlopyr, 2+Clopyralid, 2+Triclopyr, 2+Flurochloridone, 2+Flurtamone, 2+Diflufenican, 2+Picolinafen, 2+Beflubutamid, 2+Norflurazon, 2+Fluridone.

    [0280] 3+Sulcotrione, 3+Mesotrione, 3+Topramezone, 3+Tembotrione, 3+Bicyclopyrone, 3+Tefuryltrione, 3+Benzobicyclon, 3+Lancotrione, 3+Shuangzuocaotong, 3+Huanbifucaotong, 3+Sanzuohuangcaotong, 3+Benzuofucaotong, 3+Pyrasulfotole, 3+Pyrazolate, 3+Benzofenap, 3+Tolpyralate, 3+Fenquinotrione, 3+Isoxaflutole, 3+Fluroxypyr or esters thereof, 3+Halauxifen-methyl, 3+Florpyrauxifen-benzyl, 3+Quinclorac, 3+Quinmerac, 3+Chipton or salts/esters thereof, 3+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 3+MCPB or salts/esters thereof, 3+2,4-D or salts/esters thereof, 3+Dichlorprop or salts/esters thereof, 3+2,4-DB or salts/esters thereof, 3+Dicamba, 3+Picloram, 3+Trichlopyr, 3+Clopyralid, 3+Triclopyr, 3+Flurochloridone, 3+Flurtamone, 3+Diflufenican, 3+Picolinafen, 3+Beflubutamid, 3+Norflurazon, 3+Fluridone.

    [0281] 4+Sulcotrione, 4+Mesotrione, 4+Topramezone, 4+Tembotrione, 4+Bicyclopyrone, 4+Tefuryltrione, 4+Benzobicyclon, 4+Lancotrione, 4+Shuangzuocaotong, 4+Huanbifucaotong, 4+Sanzuohuangcaotong, 4+Benzuofucaotong, 4+Pyrasulfotole, 4+Pyrazolate, 4+Benzofenap, 4+Tolpyralate, 4+Fenquinotrione, 4+Isoxaflutole, 4+Fluroxypyr or esters thereof, 4+Halauxifen-methyl, 4+Florpyrauxifen-benzyl, 4+Quinclorac, 4+Quinmerac, 4+Chipton or salts/esters thereof, 4+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 4+MCPB or salts/esters thereof, 4+2,4-D or salts/esters thereof, 4+Dichlorprop or salts/esters thereof, 4+2,4-DB or salts/esters thereof, 4+Dicamba, 4+Picloram, 4+Trichlopyr, 4+Clopyralid, 4+Triclopyr, 4+Flurochloridone, 4+Flurtamone, 4+Diflufenican, 4+Picolinafen, 4+Beflubutamid, 4+Norflurazon, 4+Fluridone.

    [0282] 7+Sulcotrione, 7+Mesotrione, 7+Topramezone, 7+Tembotrione, 7+Bicyclopyrone, 7+Tefuryltrione, 7+Benzobicyclon, 7+Lancotrione, 7+Shuangzuocaotong, 7+Huanbifucaotong, 7+Sanzuohuangcaotong, 7+Benzuofucaotong, 7+Pyrasulfotole, 7+Pyrazolate, 7+Benzofenap, 7+Tolpyralate, 7+Fenquinotrione, 7+Isoxaflutole, 7+Fluroxypyr or esters thereof, 7+Halauxifen-methyl, 7+Florpyrauxifen-benzyl, 7+Quinclorac, 7+Quinmerac, 7+Chipton or salts/esters thereof, 7+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 7+MCPB or salts/esters thereof, 7+2,4-D or salts/esters thereof, 7+Dichlorprop or salts/esters thereof, 7+2,4-DB or salts/esters thereof, 7+Dicamba, 7+Picloram, 7+Trichlopyr, 7+Clopyralid, 7+Triclopyr, 7+Flurochloridone, 7+Flurtamone, 7+Diflufenican, 7+Picolinafen, 7+Beflubutamid, 7+Norflurazon, 7+Fluridone.

    [0283] 8+Sulcotrione, 8+Mesotrione, 8+Topramezone, 8+Tembotrione, 8+Bicyclopyrone, 8+Tefuryltrione, 8+Benzobicyclon, 8+Lancotrione, 8+Shuangzuocaotong, 8+Huanbifucaotong, 8+Sanzuohuangcaotong, 8+Benzuofucaotong, 8+Pyrasulfotole, 8+Pyrazolate, 8+Benzofenap, 8+Tolpyralate, 8+Fenquinotrione, 8+Isoxaflutole, 8+Fluroxypyr or esters thereof, 8+Halauxifen-methyl, 8+Florpyrauxifen-benzyl, 8+Quinclorac, 8+Quinmerac, 8+Chipton or salts/esters thereof, 8+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 8+MCPB or salts/esters thereof, 8+2,4-D or salts/esters thereof, 8+Dichlorprop or salts/esters thereof, 8+2,4-DB or salts/esters thereof, 8+Dicamba, 8+Picloram, 8+Trichlopyr, 8+Clopyralid, 8+Triclopyr, 8+Flurochloridone, 8+Flurtamone, 8+Diflufenican, 8+Picolinafen, 8+Beflubutamid, 8+Norflurazon, 8+Fluridone.

    [0284] 22+Sulcotrione, 22+Mesotrione, 22+Topramezone, 22+Tembotrione, 22+Bicyclopyrone, 22+Tefuryltrione, 22+Benzobicyclon, 22+Lancotrione, 22+Shuangzuocaotong, 22+Huanbifucaotong, 22+Sanzuohuangcaotong, 22+Benzuofucaotong, 22+Pyrasulfotole, 22+Pyrazolate, 22+Benzofenap, 22+Tolpyralate, 22+Fenquinotrione, 22+Isoxaflutole, 22+Fluroxypyr or esters thereof, 22+Halauxifen-methyl, 22+Florpyrauxifen-benzyl, 22+Quinclorac, 22+Quinmerac, 22+Chipton or salts/esters thereof, 22+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 22+MCPB or salts/esters thereof, 22+2,4-D or salts/esters thereof, 22+Dichlorprop or salts/esters thereof, 22+2,4-DB or salts/esters thereof, 22+Dicamba, 22+Picloram, 22+Trichlopyr, 22+Clopyralid, 22+Triclopyr, 22+Flurochloridone, 22+Flurtamone, 22+Diflufenican, 22+Picolinafen, 22+Beflubutamid, 22+Norflurazon, 22+Fluridone.

    [0285] 26+Sulcotrione, 26+Mesotrione, 26+Topramezone, 26+Tembotrione, 26+Bicyclopyrone, 26+Tefuryltrione, 26+Benzobicyclon, 26+Lancotrione, 26+Shuangzuocaotong, 26+Huanbifucaotong, 26+Sanzuohuangcaotong, 26+Benzuofucaotong, 26+Pyrasulfotole, 26+Pyrazolate, 26+Benzofenap, 26+Tolpyralate, 26+Fenquinotrione, 26+Isoxaflutole, 26+Fluroxypyr or esters thereof, 26+Halauxifen-methyl, 26+Florpyrauxifen-benzyl, 26+Quinclorac, 26+Quinmerac, 26+Chipton or salts/esters thereof, 26+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 26+MCPB or salts/esters thereof, 26+2,4-D or salts/esters thereof, 26+Dichlorprop or salts/esters thereof, 26+2,4-DB or salts/esters thereof, 26+Dicamba, 26+Picloram, 26+Trichlopyr, 26+Clopyralid, 26+Triclopyr, 26+Flurochloridone, 26+Flurtamone, 26+Diflufenican, 26+Picolinafen, 26+Beflubutamid, 26+Norflurazon, 26+Fluridone.

    [0286] 27+Sulcotrione, 27+Mesotrione, 27+Topramezone, 27+Tembotrione, 27+Bicyclopyrone, 27+Tefuryltrione, 27+Benzobicyclon, 27+Lancotrione, 27+Shuangzuocaotong, 27+Huanbifucaotong, 27+Sanzuohuangcaotong, 27+Benzuofucaotong, 27+Pyrasulfotole, 27+Pyrazolate, 27+Benzofenap, 27+Tolpyralate, 27+Fenquinotrione, 27+Isoxaflutole, 27+Fluroxypyr or esters thereof, 27+Halauxifen-methyl, 27+Florpyrauxifen-benzyl, 27+Quinclorac, 27+Quinmerac, 27+Chipton or salts/esters thereof, 27+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 27+MCPB or salts/esters thereof, 27+2,4-D or salts/esters thereof, 27+Dichlorprop or salts/esters thereof, 27+2,4-DB or salts/esters thereof, 27+Dicamba, 27+Picloram, 27+Trichlopyr, 27+Clopyralid, 27+Triclopyr, 27+Flurochloridone, 27+Flurtamone, 27+Diflufenican, 27+Picolinafen, 27+Beflubutamid, 27+Norflurazon, 27+Fluridone.

    [0287] 32+Sulcotrione, 32+Mesotrione, 32+Topramezone, 32+Tembotrione, 32+Bicyclopyrone, 32+Tefuryltrione, 32+Benzobicyclon, 32+Lancotrione, 32+Shuangzuocaotong, 32+Huanbifucaotong, 32+Sanzuohuangcaotong, 32+Benzuofucaotong, 32+Pyrasulfotole, 32+Pyrazolate, 32+Benzofenap, 32+Tolpyralate, 32+Fenquinotrione, 32+Isoxaflutole, 32+Fluroxypyr or esters thereof, 32+Halauxifen-methyl, 32+Florpyrauxifen-benzyl, 32+Quinclorac, 32+Quinmerac, 32+Chipton or salts/esters thereof, 32+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 32+MCPB or salts/esters thereof, 32+2,4-D or salts/esters thereof, 32+Dichlorprop or salts/esters thereof, 32+2,4-DB or salts/esters thereof, 32+Dicamba, 32+Picloram, 32+Trichlopyr, 32+Clopyralid, 32+Triclopyr, 32+Flurochloridone, 32+Flurtamone, 32+Diflufenican, 32+Picolinafen, 32+Beflubutamid, 32+Norflurazon, 32+Fluridone.

    [0288] 34+Sulcotrione, 34+Mesotrione, 34+Topramezone, 34+Tembotrione, 34+Bicyclopyrone, 34+Tefuryltrione, 34+Benzobicyclon, 34+Lancotrione, 34+Shuangzuocaotong, 34+Huanbifucaotong, 34+Sanzuohuangcaotong, 34+Benzuofucaotong, 34+Pyrasulfotole, 34+Pyrazolate, 34+Benzofenap, 34+Tolpyralate, 34+Fenquinotrione, 34+Isoxaflutole, 34+Fluroxypyr or esters thereof, 34+Halauxifen-methyl, 34+Florpyrauxifen-benzyl, 34+Quinclorac, 34+Quinmerac, 34+Chipton or salts/esters thereof, 34+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 34+MCPB or salts/esters thereof, 34+2,4-D or salts/esters thereof, 34+Dichlorprop or salts/esters thereof, 34+2,4-DB or salts/esters thereof, 34+Dicamba, 34+Picloram, 34+Trichlopyr, 34+Clopyralid, 34+Triclopyr, 34+Flurochloridone, 34+Flurtamone, 34+Diflufenican, 34+Picolinafen, 34+Beflubutamid, 34+Norflurazon, 34+Fluridone.

    [0289] 35+Sulcotrione, 35+Mesotrione, 35+Topramezone, 35+Tembotrione, 35+Bicyclopyrone, 35+Tefuryltrione, 35+Benzobicyclon, 35+Lancotrione, 35+Shuangzuocaotong, 35+Huanbifucaotong, 35+Sanzuohuangcaotong, 35+Benzuofucaotong, 35+Pyrasulfotole, 35+Pyrazolate, 35+Benzofenap, 35+Tolpyralate, 35+Fenquinotrione, 35+Isoxaflutole, 35+Fluroxypyr or esters thereof, 35+Halauxifen-methyl, 35+Florpyrauxifen-benzyl, 35+Quinclorac, 35+Quinmerac, 35+Chipton or salts/esters thereof, 35+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 35+MCPB or salts/esters thereof, 35+2,4-D or salts/esters thereof, 35+Dichlorprop or salts/esters thereof, 35+2,4-DB or salts/esters thereof, 35+Dicamba, 35+Picloram, 35+Trichlopyr, 35+Clopyralid, 35+Triclopyr, 35+Flurochloridone, 35+Flurtamone, 35+Diflufenican, 35+Picolinafen, 35+Beflubutamid, 35+Norflurazon, 35+Fluridone.

    [0290] 37+Sulcotrione, 37+Mesotrione, 37+Topramezone, 37+Tembotrione, 37+Bicyclopyrone, 37+Tefuryltrione, 37+Benzobicyclon, 37+Lancotrione, 37+Shuangzuocaotong, 37+Huanbifucaotong, 37+Sanzuohuangcaotong, 37+Benzuofucaotong, 37+Pyrasulfotole, 37+Pyrazolate, 37+Benzofenap, 37+Tolpyralate, 37+Fenquinotrione, 37+Isoxaflutole, 37+Fluroxypyr or esters thereof, 37+Halauxifen-methyl, 37+Florpyrauxifen-benzyl, 37+Quinclorac, 37+Quinmerac, 37+Chipton or salts/esters thereof, 37+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 37+MCPB or salts/esters thereof, 37+2,4-D or salts/esters thereof, 37+Dichlorprop or salts/esters thereof, 37+2,4-DB or salts/esters thereof, 37+Dicamba, 37+Picloram, 37+Trichlopyr, 37+Clopyralid, 37+Triclopyr, 37+Flurochloridone, 37+Flurtamone, 37+Diflufenican, 37+Picolinafen, 37+Beflubutamid, 37+Norflurazon, 37+Fluridone.

    [0291] 38+Sulcotrione, 38+Mesotrione, 38+Topramezone, 38+Tembotrione, 38+Bicyclopyrone, 38+Tefuryltrione, 38+Benzobicyclon, 38+Lancotrione, 38+Shuangzuocaotong, 38+Huanbifucaotong, 38+Sanzuohuangcaotong, 38+Benzuofucaotong, 38+Pyrasulfotole, 38+Pyrazolate, 38+Benzofenap, 38+Tolpyralate, 38+Fenquinotrione, 38+Isoxaflutole, 38+Fluroxypyr or esters thereof, 38+Halauxifen-methyl, 38+Florpyrauxifen-benzyl, 38+Quinclorac, 38+Quinmerac, 38+Chipton or salts/esters thereof, 38+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 38+MCPB or salts/esters thereof, 38+2,4-D or salts/esters thereof, 38+Dichlorprop or salts/esters thereof, 38+2,4-DB or salts/esters thereof, 38+Dicamba, 38+Picloram, 38+Trichlopyr, 38+Clopyralid, 38+Triclopyr, 38+Flurochloridone, 38+Flurtamone, 38+Diflufenican, 38+Picolinafen, 38+Beflubutamid, 38+Norflurazon, 38+Fluridone.

    [0292] 39+Sulcotrione, 39+Mesotrione, 39+Topramezone, 39+Tembotrione, 39+Bicyclopyrone, 39+Tefuryltrione, 39+Benzobicyclon, 39+Lancotrione, 39+Shuangzuocaotong, 39+Huanbifucaotong, 39+Sanzuohuangcaotong, 39+Benzuofucaotong, 39+Pyrasulfotole, 39+Pyrazolate, 39+Benzofenap, 39+Tolpyralate, 39+Fenquinotrione, 39+Isoxaflutole, 39+Fluroxypyr or esters thereof, 39+Halauxifen-methyl, 39+Florpyrauxifen-benzyl, 39+Quinclorac, 39+Quinmerac, 39+Chipton or salts/esters thereof, 39+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 39+MCPB or salts/esters thereof, 39+2,4-D or salts/esters thereof, 39+Dichlorprop or salts/esters thereof, 39+2,4-DB or salts/esters thereof, 39+Dicamba, 39+Picloram, 39+Trichlopyr, 39+Clopyralid, 39+Triclopyr, 39+Flurochloridone, 39+Flurtamone, 39+Diflufenican, 39+Picolinafen, 39+Beflubutamid, 39+Norflurazon, 39+Fluridone.

    [0293] 40+Sulcotrione, 40+Mesotrione, 40+Topramezone, 40+Tembotrione, 40+Bicyclopyrone, 40+Tefuryltrione, 40+Benzobicyclon, 40+Lancotrione, 40+Shuangzuocaotong, 40+Huanbifucaotong, 40+Sanzuohuangcaotong, 40+Benzuofucaotong, 40+Pyrasulfotole, 40+Pyrazolate, 40+Benzofenap, 40+Tolpyralate, 40+Fenquinotrione, 40+Isoxaflutole, 40+Fluroxypyr or esters thereof, 40+Halauxifen-methyl, 40+Florpyrauxifen-benzyl, 40+Quinclorac, 40+Quinmerac, 40+Chipton or salts/esters thereof, 40+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 40+MCPB or salts/esters thereof, 40+2,4-D or salts/esters thereof, 40+Dichlorprop or salts/esters thereof, 40+2,4-DB or salts/esters thereof, 40+Dicamba, 40+Picloram, 40+Trichlopyr, 40+Clopyralid, 40+Triclopyr, 40+Flurochloridone, 40+Flurtamone, 40+Diflufenican, 40+Picolinafen, 40+Beflubutamid, 40+Norflurazon, 40+Fluridone.

    [0294] 42+Sulcotrione, 42+Mesotrione, 42+Topramezone, 42+Tembotrione, 42+Bicyclopyrone, 42+Tefuryltrione, 42+Benzobicyclon, 42+Lancotrione, 42+Shuangzuocaotong, 42+Huanbifucaotong, 42+Sanzuohuangcaotong, 42+Benzuofucaotong, 42+Pyrasulfotole, 42+Pyrazolate, 42+Benzofenap, 42+Tolpyralate, 42+Fenquinotrione, 42+Isoxaflutole, 42+Fluroxypyr or esters thereof, 42+Halauxifen-methyl, 42+Florpyrauxifen-benzyl, 42+Quinclorac, 42+Quinmerac, 42+Chipton or salts/esters thereof, 42+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 42+MCPB or salts/esters thereof, 42+2,4-D or salts/esters thereof, 42+Dichlorprop or salts/esters thereof, 42+2,4-DB or salts/esters thereof, 42+Dicamba, 42+Picloram, 42+Trichlopyr, 42+Clopyralid, 42+Triclopyr, 42+Flurochloridone, 42+Flurtamone, 42+Diflufenican, 42+Picolinafen, 42+Beflubutamid, 42+Norflurazon, 42+Fluridone.

    [0295] 43+Sulcotrione, 43+Mesotrione, 43+Topramezone, 43+Tembotrione, 43+Bicyclopyrone, 43+Tefuryltrione, 43+Benzobicyclon, 43+Lancotrione, 43+Shuangzuocaotong, 43+Huanbifucaotong, 43+Sanzuohuangcaotong, 43+Benzuofucaotong, 43+Pyrasulfotole, 43+Pyrazolate, 43+Benzofenap, 43+Tolpyralate, 43+Fenquinotrione, 43+Isoxaflutole, 43+Fluroxypyr or esters thereof, 43+Halauxifen-methyl, 43+Florpyrauxifen-benzyl, 43+Quinclorac, 43+Quinmerac, 43+Chipton or salts/esters thereof, 43+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 43+MCPB or salts/esters thereof, 43+2,4-D or salts/esters thereof, 43+Dichlorprop or salts/esters thereof, 43+2,4-DB or salts/esters thereof, 43+Dicamba, 43+Picloram, 43+Trichlopyr, 43+Clopyralid, 43+Triclopyr, 43+Flurochloridone, 43+Flurtamone, 43+Diflufenican, 43+Picolinafen, 43+Beflubutamid, 43+Norflurazon, 43+Fluridone.

    [0296] 44+Sulcotrione, 44+Mesotrione, 44+Topramezone, 44+Tembotrione, 44+Bicyclopyrone, 44+Tefuryltrione, 44+Benzobicyclon, 44+Lancotrione, 44+Shuangzuocaotong, 44+Huanbifucaotong, 44+Sanzuohuangcaotong, 44+Benzuofucaotong, 44+Pyrasulfotole, 44+Pyrazolate, 44+Benzofenap, 44+Tolpyralate, 44+Fenquinotrione, 44+Isoxaflutole, 44+Fluroxypyr or esters thereof, 44+Halauxifen-methyl, 44+Florpyrauxifen-benzyl, 44+Quinclorac, 44+Quinmerac, 44+Chipton or salts/esters thereof, 44+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 44+MCPB or salts/esters thereof, 44+2,4-D or salts/esters thereof, 44+Dichlorprop or salts/esters thereof, 44+2,4-DB or salts/esters thereof, 44+Dicamba, 44+Picloram, 44+Trichlopyr, 44+Clopyralid, 44+Triclopyr, 44+Flurochloridone, 44+Flurtamone, 44+Diflufenican, 44+Picolinafen, 44+Beflubutamid, 44+Norflurazon, 44+Fluridone.

    [0297] 50+Sulcotrione, 50+Mesotrione, 50+Topramezone, 50+Tembotrione, 50+Bicyclopyrone, 50+Tefuryltrione, 50+Benzobicyclon, 50+Lancotrione, 50+Shuangzuocaotong, 50+Huanbifucaotong, 50+Sanzuohuangcaotong, 50+Benzuofucaotong, 50+Pyrasulfotole, 50+Pyrazolate, 50+Benzofenap, 50+Tolpyralate, 50+Fenquinotrione, 50+Isoxaflutole, 50+Fluroxypyr or esters thereof, 50+Halauxifen-methyl, 50+Florpyrauxifen-benzyl, 50+Quinclorac, 50+Quinmerac, 50+Chipton or salts/esters thereof, 50+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 50+MCPB or salts/esters thereof, 50+2,4-D or salts/esters thereof, 50+Dichlorprop or salts/esters thereof, 50+2,4-DB or salts/esters thereof, 50+Dicamba, 50+Picloram, 50+Trichlopyr, 50+Clopyralid, 50+Triclopyr, 50+Flurochloridone, 50+Flurtamone, 50+Diflufenican, 50+Picolinafen, 50+Beflubutamid, 50+Norflurazon, 50+Fluridone.

    [0298] 51+Sulcotrione, 51+Mesotrione, 51+Topramezone, 51+Tembotrione, 51+Bicyclopyrone, 51+Tefuryltrione, 51+Benzobicyclon, 51+Lancotrione, 51+Shuangzuocaotong, 51+Huanbifucaotong, 51+Sanzuohuangcaotong, 51+Benzuofucaotong, 51+Pyrasulfotole, 51+Pyrazolate, 51+Benzofenap, 51+Tolpyralate, 51+Fenquinotrione, 51+Isoxaflutole, 51+Fluroxypyr or esters thereof, 51+Halauxifen-methyl, 51+Florpyrauxifen-benzyl, 51+Quinclorac, 51+Quinmerac, 51+Chipton or salts/esters thereof, 51+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 51+MCPB or salts/esters thereof, 51+2,4-D or salts/esters thereof, 51+Dichlorprop or salts/esters thereof, 51+2,4-DB or salts/esters thereof, 51+Dicamba, 51+Picloram, 51+Trichlopyr, 51+Clopyralid, 51+Triclopyr, 51+Flurochloridone, 51+Flurtamone, 51+Diflufenican, 51+Picolinafen, 51+Beflubutamid, 51+Norflurazon, 51+Fluridone.

    [0299] 53+Sulcotrione, 53+Mesotrione, 53+Topramezone, 53+Tembotrione, 53+Bicyclopyrone, 53+Tefuryltrione, 53+Benzobicyclon, 53+Lancotrione, 53+Shuangzuocaotong, 53+Huanbifucaotong, 53+Sanzuohuangcaotong, 53+Benzuofucaotong, 53+Pyrasulfotole, 53+Pyrazolate, 53+Benzofenap, 53+Tolpyralate, 53+Fenquinotrione, 53+Isoxaflutole, 53+Fluroxypyr or esters thereof, 53+Halauxifen-methyl, 53+Florpyrauxifen-benzyl, 53+Quinclorac, 53+Quinmerac, 53+Chipton or salts/esters thereof, 53+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 53+MCPB or salts/esters thereof, 53+2,4-D or salts/esters thereof, 53+Dichlorprop or salts/esters thereof, 53+2,4-DB or salts/esters thereof, 53+Dicamba, 53+Picloram, 53+Trichlopyr, 53+Clopyralid, 53+Triclopyr, 53+Flurochloridone, 53+Flurtamone, 53+Diflufenican, 53+Picolinafen, 53+Beflubutamid, 53+Norflurazon, 53+Fluridone.

    [0300] 56+Sulcotrione, 56+Mesotrione, 56+Topramezone, 56+Tembotrione, 56+Bicyclopyrone, 56+Tefuryltrione, 56+Benzobicyclon, 56+Lancotrione, 56+Shuangzuocaotong, 56+Huanbifucaotong, 56+Sanzuohuangcaotong, 56+Benzuofucaotong, 56+Pyrasulfotole, 56+Pyrazolate, 56+Benzofenap, 56+Tolpyralate, 56+Fenquinotrione, 56+Isoxaflutole, 56+Fluroxypyr or esters thereof, 56+Halauxifen-methyl, 56+Florpyrauxifen-benzyl, 56+Quinclorac, 56+Quinmerac, 56+Chipton or salts/esters thereof, 56+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 56+MCPB or salts/esters thereof, 56+2,4-D or salts/esters thereof, 56+Dichlorprop or salts/esters thereof, 56+2,4-DB or salts/esters thereof, 56+Dicamba, 56+Picloram, 56+Trichlopyr, 56+Clopyralid, 56+Triclopyr, 56+Flurochloridone, 56+Flurtamone, 56+Diflufenican, 56+Picolinafen, 56+Beflubutamid, 56+Norflurazon, 56+Fluridone.

    [0301] 57+Sulcotrione, 57+Mesotrione, 57+Topramezone, 57+Tembotrione, 57+Bicyclopyrone, 57+Tefuryltrione, 57+Benzobicyclon, 57+Lancotrione, 57+Shuangzuocaotong, 57+Huanbifucaotong, 57+Sanzuohuangcaotong, 57+Benzuofucaotong, 57+Pyrasulfotole, 57+Pyrazolate, 57+Benzofenap, 57+Tolpyralate, 57+Fenquinotrione, 57+Isoxaflutole, 57+Fluroxypyr or esters thereof, 57+Halauxifen-methyl, 57+Florpyrauxifen-benzyl, 57+Quinclorac, 57+Quinmerac, 57+Chipton or salts/esters thereof, 57+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 57+MCPB or salts/esters thereof, 57+2,4-D or salts/esters thereof, 57+Dichlorprop or salts/esters thereof, 57+2,4-DB or salts/esters thereof, 57+Dicamba, 57+Picloram, 57+Trichlopyr, 57+Clopyralid, 57+Triclopyr, 57+Flurochloridone, 57+Flurtamone, 57+Diflufenican, 57+Picolinafen, 57+Beflubutamid, 57+Norflurazon, 57+Fluridone.

    [0302] 58+Sulcotrione, 58+Mesotrione, 58+Topramezone, 58+Tembotrione, 58+Bicyclopyrone, 58+Tefuryltrione, 58+Benzobicyclon, 58+Lancotrione, 58+Shuangzuocaotong, 58+Huanbifucaotong, 58+Sanzuohuangcaotong, 58+Benzuofucaotong, 58+Pyrasulfotole, 58+Pyrazolate, 58+Benzofenap, 58+Tolpyralate, 58+Fenquinotrione, 58+Isoxaflutole, 58+Fluroxypyr or esters thereof, 58+Halauxifen-methyl, 58+Florpyrauxifen-benzyl, 58+Quinclorac, 58+Quinmerac, 58+Chipton or salts/esters thereof, 58+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 58+MCPB or salts/esters thereof, 58+2,4-D or salts/esters thereof, 58+Dichlorprop or salts/esters thereof, 58+2,4-DB or salts/esters thereof, 58+Dicamba, 58+Picloram, 58+Trichlopyr, 58+Clopyralid, 58+Triclopyr, 58+Flurochloridone, 58+Flurtamone, 58+Diflufenican, 58+Picolinafen, 58+Beflubutamid, 58+Norflurazon, 58+Fluridone.

    [0303] 59+Sulcotrione, 59+Mesotrione, 59+Topramezone, 59+Tembotrione, 59+Bicyclopyrone, 59+Tefuryltrione, 59+Benzobicyclon, 59+Lancotrione, 59+Shuangzuocaotong, 59+Huanbifucaotong, 59+Sanzuohuangcaotong, 59+Benzuofucaotong, 59+Pyrasulfotole, 59+Pyrazolate, 59+Benzofenap, 59+Tolpyralate, 59+Fenquinotrione, 59+Isoxaflutole, 59+Fluroxypyr or esters thereof, 59+Halauxifen-methyl, 59+Florpyrauxifen-benzyl, 59+Quinclorac, 59+Quinmerac, 59+Chipton or salts/esters thereof, 59+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 59+MCPB or salts/esters thereof, 59+2,4-D or salts/esters thereof, 59+Dichlorprop or salts/esters thereof, 59+2,4-DB or salts/esters thereof, 59+Dicamba, 59+Picloram, 59+Trichlopyr, 59+Clopyralid, 59+Triclopyr, 59+Flurochloridone, 59+Flurtamone, 59+Diflufenican, 59+Picolinafen, 59+Beflubutamid, 59+Norflurazon, 59+Fluridone.

    [0304] 60+Sulcotrione, 60+Mesotrione, 60+Topramezone, 60+Tembotrione, 60+Bicyclopyrone, 60+Tefuryltrione, 60+Benzobicyclon, 60+Lancotrione, 60+Shuangzuocaotong, 60+Huanbifucaotong, 60+Sanzuohuangcaotong, 60+Benzuofucaotong, 60+Pyrasulfotole, 60+Pyrazolate, 60+Benzofenap, 60+Tolpyralate, 60+Fenquinotrione, 60+Isoxaflutole, 60+Fluroxypyr or esters thereof, 60+Halauxifen-methyl, 60+Florpyrauxifen-benzyl, 60+Quinclorac, 60+Quinmerac, 60+Chipton or salts/esters thereof, 60+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 60+MCPB or salts/esters thereof, 60+2,4-D or salts/esters thereof, 60+Dichlorprop or salts/esters thereof, 60+2,4-DB or salts/esters thereof, 60+Dicamba, 60+Picloram, 60+Trichlopyr, 60+Clopyralid, 60+Triclopyr, 60+Flurochloridone, 60+Flurtamone, 60+Diflufenican, 60+Picolinafen, 60+Beflubutamid, 60+Norflurazon, 60+Fluridone.

    [0305] 66+Sulcotrione, 66+Mesotrione, 66+Topramezone, 66+Tembotrione, 66+Bicyclopyrone, 66+Tefuryltrione, 66+Benzobicyclon, 66+Lancotrione, 66+Shuangzuocaotong, 66+Huanbifucaotong, 66+Sanzuohuangcaotong, 66+Benzuofucaotong, 66+Pyrasulfotole, 66+Pyrazolate, 66+Benzofenap, 66+Tolpyralate, 66+Fenquinotrione, 66+Isoxaflutole, 66+Fluroxypyr or esters thereof, 66+Halauxifen-methyl, 66+Florpyrauxifen-benzyl, 66+Quinclorac, 66+Quinmerac, 66+Chipton or salts/esters thereof, 66+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 66+MCPB or salts/esters thereof, 66+2,4-D or salts/esters thereof, 66+Dichlorprop or salts/esters thereof, 66+2,4-DB or salts/esters thereof, 66+Dicamba, 66+Picloram, 66+Trichlopyr, 66+Clopyralid, 66+Triclopyr, 66+Flurochloridone, 66+Flurtamone, 66+Diflufenican, 66+Picolinafen, 66+Beflubutamid, 66+Norflurazon, 66+Fluridone.

    [0306] 68+Sulcotrione, 68+Mesotrione, 68+Topramezone, 68+Tembotrione, 68+Bicyclopyrone, 68+Tefuryltrione, 68+Benzobicyclon, 68+Lancotrione, 68+Shuangzuocaotong, 68+Huanbifucaotong, 68+Sanzuohuangcaotong, 68+Benzuofucaotong, 68+Pyrasulfotole, 68+Pyrazolate, 68+Benzofenap, 68+Tolpyralate, 68+Fenquinotrione, 68+Isoxaflutole, 68+Fluroxypyr or esters thereof, 68+Halauxifen-methyl, 68+Florpyrauxifen-benzyl, 68+Quinclorac, 68+Quinmerac, 68+Chipton or salts/esters thereof, 68+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 68+MCPB or salts/esters thereof, 68+2,4-D or salts/esters thereof, 68+Dichlorprop or salts/esters thereof, 68+2,4-DB or salts/esters thereof, 68+Dicamba, 68+Picloram, 68+Trichlopyr, 68+Clopyralid, 68+Triclopyr, 68+Flurochloridone, 68+Flurtamone, 68+Diflufenican, 68+Picolinafen, 68+Beflubutamid, 68+Norflurazon, 68+Fluridone.

    [0307] 77+Sulcotrione, 77+Mesotrione, 77+Topramezone, 77+Tembotrione, 77+Bicyclopyrone, 77+Tefuryltrione, 77+Benzobicyclon, 77+Lancotrione, 77+Shuangzuocaotong, 77+Huanbifucaotong, 77+Sanzuohuangcaotong, 77+Benzuofucaotong, 77+Pyrasulfotole, 77+Pyrazolate, 77+Benzofenap, 77+Tolpyralate, 77+Fenquinotrione, 77+Isoxaflutole, 77+Fluroxypyr or esters thereof, 77+Halauxifen-methyl, 77+Florpyrauxifen-benzyl, 77+Quinclorac, 77+Quinmerac, 77+Chipton or salts/esters thereof, 77+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 77+MCPB or salts/esters thereof, 77+2,4-D or salts/esters thereof, 77+Dichlorprop or salts/esters thereof, 77+2,4-DB or salts/esters thereof, 77+Dicamba, 77+Picloram, 77+Trichlopyr, 77+Clopyralid, 77+Triclopyr, 77+Flurochloridone, 77+Flurtamone, 77+Diflufenican, 77+Picolinafen, 77+Beflubutamid, 77+Norflurazon, 77+Fluridone.

    [0308] 79+Sulcotrione, 79+Mesotrione, 79+Topramezone, 79+Tembotrione, 79+Bicyclopyrone, 79+Tefuryltrione, 79+Benzobicyclon, 79+Lancotrione, 79+Shuangzuocaotong, 79+Huanbifucaotong, 79+Sanzuohuangcaotong, 79+Benzuofucaotong, 79+Pyrasulfotole, 79+Pyrazolate, 79+Benzofenap, 79+Tolpyralate, 79+Fenquinotrione, 79+Isoxaflutole, 79+Fluroxypyr or esters thereof, 79+Halauxifen-methyl, 79+Florpyrauxifen-benzyl, 79+Quinclorac, 79+Quinmerac, 79+Chipton or salts/esters thereof, 79+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 79+MCPB or salts/esters thereof, 79+2,4-D or salts/esters thereof, 79+Dichlorprop or salts/esters thereof, 79+2,4-DB or salts/esters thereof, 79+Dicamba, 79+Picloram, 79+Trichlopyr, 79+Clopyralid, 79+Triclopyr, 79+Flurochloridone, 79+Flurtamone, 79+Diflufenican, 79+Picolinafen, 79+Beflubutamid, 79+Norflurazon, 79+Fluridone.

    [0309] 87+Sulcotrione, 87+Mesotrione, 87+Topramezone, 87+Tembotrione, 87+Bicyclopyrone, 87+Tefuryltrione, 87+Benzobicyclon, 87+Lancotrione, 87+Shuangzuocaotong, 87+Huanbifucaotong, 87+Sanzuohuangcaotong, 87+Benzuofucaotong, 87+Pyrasulfotole, 87+Pyrazolate, 87+Benzofenap, 87+Tolpyralate, 87+Fenquinotrione, 87+Isoxaflutole, 87+Fluroxypyr or esters thereof, 87+Halauxifen-methyl, 87+Florpyrauxifen-benzyl, 87+Quinclorac, 87+Quinmerac, 87+Chipton or salts/esters thereof, 87+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 87+MCPB or salts/esters thereof, 87+2,4-D or salts/esters thereof, 87+Dichlorprop or salts/esters thereof, 87+2,4-DB or salts/esters thereof, 87+Dicamba, 87+Picloram, 87+Trichlopyr, 87+Clopyralid, 87+Triclopyr, 87+Flurochloridone, 87+Flurtamone, 87+Diflufenican, 87+Picolinafen, 87+Beflubutamid, 87+Norflurazon, 87+Fluridone.

    [0310] 92+Sulcotrione, 92+Mesotrione, 92+Topramezone, 92+Tembotrione, 92+Bicyclopyrone, 92+Tefuryltrione, 92+Benzobicyclon, 92+Lancotrione, 92+Shuangzuocaotong, 92+Huanbifucaotong, 92+Sanzuohuangcaotong, 92+Benzuofucaotong, 92+Pyrasulfotole, 92+Pyrazolate, 92+Benzofenap, 92+Tolpyralate, 92+Fenquinotrione, 92+Isoxaflutole, 92+Fluroxypyr or esters thereof, 92+Halauxifen-methyl, 92+Florpyrauxifen-benzyl, 92+Quinclorac, 92+Quinmerac, 92+Chipton or salts/esters thereof, 92+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 92+MCPB or salts/esters thereof, 92+2,4-D or salts/esters thereof, 92+Dichlorprop or salts/esters thereof, 92+2,4-DB or salts/esters thereof, 92+Dicamba, 92+Picloram, 92+Trichlopyr, 92+Clopyralid, 92+Triclopyr, 92+Flurochloridone, 92+Flurtamone, 92+Diflufenican, 92+Picolinafen, 92+Beflubutamid, 92+Norflurazon, 92+Fluridone. 191+Sulcotrione, 191+Mesotrione, 191+Topramezone, 191+Tembotrione, 191+Bicyclopyrone, 191+Tefuryltrione, 191+Benzobicyclon, 191+Lancotrione, 191+Shuangzuocaotong, 191+Huanbifucaotong, 191+Sanzuohuangcaotong, 191+Benzuofucaotong,

    [0311] 191+Pyrasulfotole, 191+Pyrazolate, 191+Benzofenap, 191+Tolpyralate, 191+Fenquinotrione, 191+Isoxaflutole, 191+Fluroxypyr or esters thereof, 191+Halauxifen-methyl, 191+Florpyrauxifen-benzyl, 191+Quinclorac, 191+Quinmerac, 191+Chipton or salts/esters thereof, 191+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 191+MCPB or salts/esters thereof, 191+2,4-D or salts/esters thereof, 191+Dichlorprop or salts/esters thereof, 191+2,4-DB or salts/esters thereof, 191+Dicamba, 191+Picloram, 191+Trichlopyr, 191+Clopyralid, 191+Triclopyr, 191+Flurochloridone, 191+Flurtamone, 191+Diflufenican, 191+Picolinafen, 191+Beflubutamid, 191+Norflurazon, 191+Fluridone.

    [0312] 202+Sulcotrione, 202+Mesotrione, 202+Topramezone, 202+Tembotrione, 202+Bicyclopyrone, 202+Tefuryltrione, 202+Benzobicyclon, 202+Lancotrione, 202+Shuangzuocaotong, 202+Huanbifucaotong, 202+Sanzuohuangcaotong, 202+Benzuofucaotong, 202+Pyrasulfotole, 202+Pyrazolate, 202+Benzofenap, 202+Tolpyralate, 202+Fenquinotrione, 202+Isoxaflutole, 202+Fluroxypyr or esters thereof, 202+Halauxifen-methyl, 202+Florpyrauxifen-benzyl, 202+Quinclorac, 202+Quinmerac, 202+Chipton or salts/esters thereof, 202+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 202+MCPB or salts/esters thereof, 202+2,4-D or salts/esters thereof, 202+Dichlorprop or salts/esters thereof, 202+2,4-DB or salts/esters thereof, 202+Dicamba, 202+Picloram, 202+Trichlopyr, 202+Clopyralid, 202+Triclopyr, 202+Flurochloridone, 202+Flurtamone, 202+Diflufenican, 202+Picolinafen, 202+Beflubutamid, 202+Norflurazon, 202+Fluridone.

    [0313] 206+Sulcotrione, 206+Mesotrione, 206+Topramezone, 206+Tembotrione, 206+Bicyclopyrone, 206+Tefuryltrione, 206+Benzobicyclon, 206+Lancotrione, 206+Shuangzuocaotong, 206+Huanbifucaotong, 206+Sanzuohuangcaotong, 206+Benzuofucaotong, 206+Pyrasulfotole, 206+Pyrazolate, 206+Benzofenap, 206+Tolpyralate, 206+Fenquinotrione, 206+Isoxaflutole, 206+Fluroxypyr or esters thereof, 206+Halauxifen-methyl, 206+Florpyrauxifen-benzyl, 206+Quinclorac, 206+Quinmerac, 206+Chipton or salts/esters thereof, 206+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 206+MCPB or salts/esters thereof, 206+2,4-D or salts/esters thereof, 206+Dichlorprop or salts/esters thereof, 206+2,4-DB or salts/esters thereof, 206+Dicamba, 206+Picloram, 206+Trichlopyr, 206+Clopyralid, 206+Triclopyr, 206+Flurochloridone, 206+Flurtamone, 206+Diflufenican, 206+Picolinafen, 206+Beflubutamid, 206+Norflurazon, 206+Fluridone. 207+Sulcotrione, 207+Mesotrione, 207+Topramezone, 207+Tembotrione, 207+Bicyclopyrone, 207+Tefuryltrione, 207+Benzobicyclon, 207+Lancotrione, 207+Shuangzuocaotong, 207+Huanbifucaotong, 207+Sanzuohuangcaotong, 207+Benzuofucaotong,

    [0314] 207+Pyrasulfotole, 207+Pyrazolate, 207+Benzofenap, 207+Tolpyralate, 207+Fenquinotrione, 207+Isoxaflutole, 207+Fluroxypyr or esters thereof, 207+Halauxifen-methyl, 207+Florpyrauxifen-benzyl, 207+Quinclorac, 207+Quinmerac, 207+Chipton or salts/esters thereof, 207+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 207+MCPB or salts/esters thereof, 207+2,4-D or salts/esters thereof, 207+Dichlorprop or salts/esters thereof, 207+2,4-DB or salts/esters thereof, 207+Dicamba, 207+Picloram, 207+Trichlopyr, 207+Clopyralid, 207+Triclopyr, 207+Flurochloridone, 207+Flurtamone, 207+Diflufenican, 207+Picolinafen, 207+Beflubutamid, 207+Norflurazon, 207+Fluridone.

    [0315] 220+Sulcotrione, 220+Mesotrione, 220+Topramezone, 220+Tembotrione, 220+Bicyclopyrone, 220+Tefuryltrione, 220+Benzobicyclon, 220+Lancotrione, 220+Shuangzuocaotong, 220+Huanbifucaotong, 220+Sanzuohuangcaotong, 220+Benzuofucaotong, 220+Pyrasulfotole, 220+Pyrazolate, 220+Benzofenap, 220+Tolpyralate, 220+Fenquinotrione, 220+Isoxaflutole, 220+Fluroxypyr or esters thereof, 220+Halauxifen-methyl, 220+Florpyrauxifen-benzyl, 220+Quinclorac, 220+Quinmerac, 220+Chipton or salts/esters thereof, 220+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 220+MCPB or salts/esters thereof, 220+2,4-D or salts/esters thereof, 220+Dichlorprop or salts/esters thereof, 220+2,4-DB or salts/esters thereof, 220+Dicamba, 220+Picloram, 220+Trichlopyr, 220+Clopyralid, 220+Triclopyr, 220+Flurochloridone, 220+Flurtamone, 220+Diflufenican, 220+Picolinafen, 220+Beflubutamid, 220+Norflurazon, 220+Fluridone.

    [0316] 278+Sulcotrione, 278+Mesotrione, 278+Topramezone, 278+Tembotrione, 278+Bicyclopyrone, 278+Tefuryltrione, 278+Benzobicyclon, 278+Lancotrione, 278+Shuangzuocaotong, 278+Huanbifucaotong, 278+Sanzuohuangcaotong, 278+Benzuofucaotong, 278+Pyrasulfotole, 278+Pyrazolate, 278+Benzofenap, 278+Tolpyralate, 278+Fenquinotrione, 278+Isoxaflutole, 278+Fluroxypyr or esters thereof, 278+Halauxifen-methyl, 278+Florpyrauxifen-benzyl, 278+Quinclorac, 278+Quinmerac, 278+Chipton or salts/esters thereof, 278+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 278+MCPB or salts/esters thereof, 278+2,4-D or salts/esters thereof, 278+Dichlorprop or salts/esters thereof, 278+2,4-DB or salts/esters thereof, 278+Dicamba, 278+Picloram, 278+Trichlopyr, 278+Clopyralid, 278+Triclopyr, 278+Flurochloridone, 278+Flurtamone, 278+Diflufenican, 278+Picolinafen, 278+Beflubutamid, 278+Norflurazon, 278+Fluridone.

    [0317] 341+Sulcotrione, 341+Mesotrione, 341+Topramezone, 341+Tembotrione, 341+Bicyclopyrone, 341+Tefuryltrione, 341+Benzobicyclon, 341+Lancotrione, 341+Shuangzuocaotong, 341+Huanbifucaotong, 341+Sanzuohuangcaotong, 341+Benzuofucaotong, 341+Pyrasulfotole, 341+Pyrazolate, 341+Benzofenap, 341+Tolpyralate, 341+Fenquinotrione, 341+Isoxaflutole, 341+Fluroxypyr or esters thereof, 341+Halauxifen-methyl, 341+Florpyrauxifen-benzyl, 341+Quinclorac, 341+Quinmerac, 341+Chipton or salts/esters thereof, 341+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 341+MCPB or salts/esters thereof, 341+2,4-D or salts/esters thereof, 341+Dichlorprop or salts/esters thereof, 341+2,4-DB or salts/esters thereof, 341+Dicamba, 341+Picloram, 341+Trichlopyr, 341+Clopyralid, 341+Triclopyr, 341+Flurochloridone, 341+Flurtamone, 341+Diflufenican, 341+Picolinafen, 341+Beflubutamid, 341+Norflurazon, 341+Fluridone.

    [0318] 732+Sulcotrione, 732+Mesotrione, 732+Topramezone, 732+Tembotrione, 732+Bicyclopyrone, 732+Tefuryltrione, 732+Benzobicyclon, 732+Lancotrione, 732+Shuangzuocaotong, 732+Huanbifucaotong, 732+Sanzuohuangcaotong, 732+Benzuofucaotong, 732+Pyrasulfotole, 732+Pyrazolate, 732+Benzofenap, 732+Tolpyralate, 732+Fenquinotrione, 732+Isoxaflutole, 732+Fluroxypyr or esters thereof, 732+Halauxifen-methyl, 732+Florpyrauxifen-benzyl, 732+Quinclorac, 732+Quinmerac, 732+Chipton or salts/esters thereof, 732+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 732+MCPB or salts/esters thereof, 732+2,4-D or salts/esters thereof, 732+Dichlorprop or salts/esters thereof, 732+2,4-DB or salts/esters thereof, 732+Dicamba, 732+Picloram, 732+Trichlopyr, 732+Clopyralid, 732+Triclopyr, 732+Flurochloridone, 732+Flurtamone, 732+Diflufenican, 732+Picolinafen, 732+Beflubutamid, 732+Norflurazon, 732+Fluridone.

    [0319] 733+Sulcotrione, 733+Mesotrione, 733+Topramezone, 733+Tembotrione, 733+Bicyclopyrone, 733+Tefuryltrione, 733+Benzobicyclon, 733+Lancotrione, 733+Shuangzuocaotong, 733+Huanbifucaotong, 733+Sanzuohuangcaotong, 733+Benzuofucaotong, 733+Pyrasulfotole, 733+Pyrazolate, 733+Benzofenap, 733+Tolpyralate, 733+Fenquinotrione, 733+Isoxaflutole, 733+Fluroxypyr or esters thereof, 733+Halauxifen-methyl, 733+Florpyrauxifen-benzyl, 733+Quinclorac, 733+Quinmerac, 733+Chipton or salts/esters thereof, 733+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 733+MCPB or salts/esters thereof, 733+2,4-D or salts/esters thereof, 733+Dichlorprop or salts/esters thereof, 733+2,4-DB or salts/esters thereof, 733+Dicamba, 733+Picloram, 733+Trichlopyr, 733+Clopyralid, 733+Triclopyr, 733+Flurochloridone, 733+Flurtamone, 733+Diflufenican, 733+Picolinafen, 733+Beflubutamid, 733+Norflurazon, 733+Fluridone.

    [0320] 734+Sulcotrione, 734+Mesotrione, 734+Topramezone, 734+Tembotrione, 734+Bicyclopyrone, 734+Tefuryltrione, 734+Benzobicyclon, 734+Lancotrione, 734+Shuangzuocaotong, 734+Huanbifucaotong, 734+Sanzuohuangcaotong, 734+Benzuofucaotong, 734+Pyrasulfotole, 734+Pyrazolate, 734+Benzofenap, 734+Tolpyralate, 734+Fenquinotrione, 734+Isoxaflutole, 734+Fluroxypyr or esters thereof, 734+Halauxifen-methyl, 734+Florpyrauxifen-benzyl, 734+Quinclorac, 734+Quinmerac, 734+Chipton or salts/esters thereof, 734+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 734+MCPB or salts/esters thereof, 734+2,4-D or salts/esters thereof, 734+Dichlorprop or salts/esters thereof, 734+2,4-DB or salts/esters thereof, 734+Dicamba, 734+Picloram, 734+Trichlopyr, 734+Clopyralid, 734+Triclopyr, 734+Flurochloridone, 734+Flurtamone, 734+Diflufenican, 734+Picolinafen, 734+Beflubutamid, 734+Norflurazon, 734+Fluridone.

    [0321] 735+Sulcotrione, 735+Mesotrione, 735+Topramezone, 735+Tembotrione, 735+Bicyclopyrone, 735+Tefuryltrione, 735+Benzobicyclon, 735+Lancotrione, 735+Shuangzuocaotong, 735+Huanbifucaotong, 735+Sanzuohuangcaotong, 735+Benzuofucaotong, 735+Pyrasulfotole, 735+Pyrazolate, 735+Benzofenap, 735+Tolpyralate, 735+Fenquinotrione, 735+Isoxaflutole, 735+Fluroxypyr or esters thereof, 735+Halauxifen-methyl, 735+Florpyrauxifen-benzyl, 735+Quinclorac, 735+Quinmerac, 735+Chipton or salts/esters thereof, 735+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 735+MCPB or salts/esters thereof, 735+2,4-D or salts/esters thereof, 735+Dichlorprop or salts/esters thereof, 735+2,4-DB or salts/esters thereof, 735+Dicamba, 735+Picloram, 735+Trichlopyr, 735+Clopyralid, 735+Triclopyr, 735+Flurochloridone, 735+Flurtamone, 735+Diflufenican, 735+Picolinafen, 735+Beflubutamid, 735+Norflurazon, 735+Fluridone. 736+Sulcotrione, 736+Mesotrione, 736+Topramezone, 736+Tembotrione, 736+Bicyclopyrone, 736+Tefuryltrione, 736+Benzobicyclon, 736+Lancotrione, 736+Shuangzuocaotong, 736+Huanbifucaotong, 736+Sanzuohuangcaotong, 736+Benzuofucaotong,

    [0322] 736+Pyrasulfotole, 736+Pyrazolate, 736+Benzofenap, 736+Tolpyralate, 736+Fenquinotrione, 736+Isoxaflutole, 736+Fluroxypyr or esters thereof, 736+Halauxifen-methyl, 736+Florpyrauxifen-benzyl, 736+Quinclorac, 736+Quinmerac, 736+Chipton or salts/esters thereof, 736+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 736+MCPB or salts/esters thereof, 736+2,4-D or salts/esters thereof, 736+Dichlorprop or salts/esters thereof, 736+2,4-DB or salts/esters thereof, 736+Dicamba, 736+Picloram, 736+Trichlopyr, 736+Clopyralid, 736+Triclopyr, 736+Flurochloridone, 736+Flurtamone, 736+Diflufenican, 736+Picolinafen, 736+Beflubutamid, 736+Norflurazon, 736+Fluridone.

    [0323] 737+Sulcotrione, 737+Mesotrione, 737+Topramezone, 737+Tembotrione, 737+Bicyclopyrone, 737+Tefuryltrione, 737+Benzobicyclon, 737+Lancotrione, 737+Shuangzuocaotong, 737+Huanbifucaotong, 737+Sanzuohuangcaotong, 737+Benzuofucaotong, 737+Pyrasulfotole, 737+Pyrazolate, 737+Benzofenap, 737+Tolpyralate, 737+Fenquinotrione, 737+Isoxaflutole, 737+Fluroxypyr or esters thereof, 737+Halauxifen-methyl, 737+Florpyrauxifen-benzyl, 737+Quinclorac, 737+Quinmerac, 737+Chipton or salts/esters thereof, 737+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 737+MCPB or salts/esters thereof, 737+2,4-D or salts/esters thereof, 737+Dichlorprop or salts/esters thereof, 737+2,4-DB or salts/esters thereof, 737+Dicamba, 737+Picloram, 737+Trichlopyr, 737+Clopyralid, 737+Triclopyr, 737+Flurochloridone, 737+Flurtamone, 737+Diflufenican, 737+Picolinafen, 737+Beflubutamid, 737+Norflurazon, 737+Fluridone.

    [0324] 738+Sulcotrione, 738+Mesotrione, 738+Topramezone, 738+Tembotrione, 738+Bicyclopyrone, 738+Tefuryltrione, 738+Benzobicyclon, 738+Lancotrione, 738+Shuangzuocaotong, 738+Huanbifucaotong, 738+Sanzuohuangcaotong, 738+Benzuofucaotong, 738+Pyrasulfotole, 738+Pyrazolate, 738+Benzofenap, 738+Tolpyralate, 738+Fenquinotrione, 738+Isoxaflutole, 738+Fluroxypyr or esters thereof, 738+Halauxifen-methyl, 738+Florpyrauxifen-benzyl, 738+Quinclorac, 738+Quinmerac, 738+Chipton or salts/esters thereof, 738+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 738+MCPB or salts/esters thereof, 738+2,4-D or salts/esters thereof, 738+Dichlorprop or salts/esters thereof, 738+2,4-DB or salts/esters thereof, 738+Dicamba, 738+Picloram, 738+Trichlopyr, 738+Clopyralid, 738+Triclopyr, 738+Flurochloridone, 738+Flurtamone, 738+Diflufenican, 738+Picolinafen, 738+Beflubutamid, 738+Norflurazon, 738+Fluridone.

    [0325] 739+Sulcotrione, 739+Mesotrione, 739+Topramezone, 739+Tembotrione, 739+Bicyclopyrone, 739+Tefuryltrione, 739+Benzobicyclon, 739+Lancotrione, 739+Shuangzuocaotong, 739+Huanbifucaotong, 739+S anzuohuangc aotong, 739+Benzuofucaotong, 739+Pyrasulfotole, 739+Pyrazolate, 739+Benzofenap, 739+Tolpyralate, 739+Fenquinotrione, 739+Isoxaflutole, 739+Fluroxypyr or esters thereof, 739+Halauxifen-methyl, 739+Florpyrauxifen-benzyl, 739+Quinclorac, 739+Quinmerac, 739+Chipton or salts/esters thereof, 739+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 739+MCPB or salts/esters thereof, 739+2,4-D or salts/esters thereof, 739+Dichlorprop or salts/esters thereof, 739+2,4-DB or salts/esters thereof, 739+Dicamba, 739+Picloram, 739+Trichlopyr, 739+Clopyralid, 739+Triclopyr, 739+Flurochloridone, 739+Flurtamone, 739+Diflufenican, 739+Picolinafen, 739+Beflubutamid, 739+Norflurazon, 739+Fluridone.

    [0326] 740+Sulcotrione, 740+Mesotrione, 740+Topramezone, 740+Tembotrione, 740+Bicyclopyrone, 740+Tefuryltrione, 740+Benzobicyclon, 740+Lancotrione, 740+Shuangzuocaotong, 740+Huanbifucaotong, 740+Sanzuohuangcaotong, 740+Benzuofucaotong, 740+Pyrasulfotole, 740+Pyrazolate, 740+Benzofenap, 740+Tolpyralate, 740+Fenquinotrione, 740+Isoxaflutole, 740+Fluroxypyr or esters thereof, 740+Halauxifen-methyl, 740+Florpyrauxifen-benzyl, 740+Quinclorac, 740+Quinmerac, 740+Chipton or salts/esters thereof, 740+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 740+MCPB or salts/esters thereof, 740+2,4-D or salts/esters thereof, 740+Dichlorprop or salts/esters thereof, 740+2,4-DB or salts/esters thereof, 740+Dicamba, 740+Picloram, 740+Trichlopyr, 740+Clopyralid, 740+Triclopyr, 740+Flurochloridone, 740+Flurtamone, 740+Diflufenican, 740+Picolinafen, 740+Beflubutamid, 740+Norflurazon, 740+Fluridone.

    [0327] 741+Sulcotrione, 741+Mesotrione, 741+Topramezone, 741+Tembotrione, 741+Bicyclopyrone, 741+Tefuryltrione, 741+Benzobicyclon, 741+Lancotrione, 741+Shuangzuocaotong, 741+Huanbifucaotong, 741+Sanzuohuangcaotong, 741+Benzuofucaotong, 741+Pyrasulfotole, 741+Pyrazolate, 741+Benzofenap, 741+Tolpyralate, 741+Fenquinotrione, 741+Isoxaflutole, 741+Fluroxypyr or esters thereof, 741+Halauxifen-methyl, 741+Florpyrauxifen-benzyl, 741+Quinclorac, 741+Quinmerac, 741+Chipton or salts/esters thereof, 741+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 741+MCPB or salts/esters thereof, 741+2,4-D or salts/esters thereof, 741+Dichlorprop or salts/esters thereof, 741+2,4-DB or salts/esters thereof, 741+Dicamba, 741+Picloram, 741+Trichlopyr, 741+Clopyralid, 741+Triclopyr, 741+Flurochloridone, 741+Flurtamone, 741+Diflufenican, 741+Picolinafen, 741+Beflubutamid, 741+Norflurazon, 741+Fluridone.

    [0328] 742+Sulcotrione, 742+Mesotrione, 742+Topramezone, 742+Tembotrione, 742+Bicyclopyrone, 742+Tefuryltrione, 742+Benzobicyclon, 742+Lancotrione, 742+Shuangzuocaotong, 742+Huanbifucaotong, 742+Sanzuohuangcaotong, 742+Benzuofucaotong, 742+Pyrasulfotole, 742+Pyrazolate, 742+Benzofenap, 742+Tolpyralate, 742+Fenquinotrione, 742+Isoxaflutole, 742+Fluroxypyr or esters thereof, 742+Halauxifen-methyl, 742+Florpyrauxifen-benzyl, 742+Quinclorac, 742+Quinmerac, 742+Chipton or salts/esters thereof, 742+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 742+MCPB or salts/esters thereof, 742+2,4-D or salts/esters thereof, 742+Dichlorprop or salts/esters thereof, 742+2,4-DB or salts/esters thereof, 742+Dicamba, 742+Picloram, 742+Trichlopyr, 742+Clopyralid, 742+Triclopyr, 742+Flurochloridone, 742+Flurtamone, 742+Diflufenican, 742+Picolinafen, 742+Beflubutamid, 742+Norflurazon, 742+Fluridone.

    [0329] 743+Sulcotrione, 743+Mesotrione, 743+Topramezone, 743+Tembotrione, 743+Bicyclopyrone, 743+Tefuryltrione, 743+Benzobicyclon, 743+Lancotrione, 743+Shuangzuocaotong, 743+Huanbifucaotong, 743+S anzuohuangc aotong, 743+Benzuofucaotong, 743+Pyrasulfotole, 743+Pyrazolate, 743+Benzofenap, 743+Tolpyralate, 743+Fenquinotrione, 743+Isoxaflutole, 743+Fluroxypyr or esters thereof, 743+Halauxifen-methyl, 743+Florpyrauxifen-benzyl, 743+Quinclorac, 743+Quinmerac, 743+Chipton or salts/esters thereof, 743+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 743+MCPB or salts/esters thereof, 743+2,4-D or salts/esters thereof, 743+Dichlorprop or salts/esters thereof, 743+2,4-DB or salts/esters thereof, 743+Dicamba, 743+Picloram, 743+Trichlopyr, 743+Clopyralid, 743+Triclopyr, 743+Flurochloridone, 743+Flurtamone, 743+Diflufenican, 743+Picolinafen, 743+Beflubutamid, 743+Norflurazon, 743+Fluridone.

    [0330] 744+Sulcotrione, 744+Mesotrione, 744+Topramezone, 744+Tembotrione, 744+Bicyclopyrone, 744+Tefuryltrione, 744+Benzobicyclon, 744+Lancotrione, 744+Shuangzuocaotong, 744+Huanbifucaotong, 744+Sanzuohuangcaotong, 744+Benzuofucaotong, 744+Pyrasulfotole, 744+Pyrazolate, 744+Benzofenap, 744+Tolpyralate, 744+Fenquinotrione, 744+Isoxaflutole, 744+Fluroxypyr or esters thereof, 744+Halauxifen-methyl, 744+Florpyrauxifen-benzyl, 744+Quinclorac, 744+Quinmerac, 744+Chipton or salts/esters thereof, 744+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 744+MCPB or salts/esters thereof, 744+2,4-D or salts/esters thereof, 744+Dichlorprop or salts/esters thereof, 744+2,4-DB or salts/esters thereof, 744+Dicamba, 744+Picloram, 744+Trichlopyr, 744+Clopyralid, 744+Triclopyr, 744+Flurochloridone, 744+Flurtamone, 744+Diflufenican, 744+Picolinafen, 744+Beflubutamid, 744+Norflurazon, 744+Fluridone.

    [0331] 745+Sulcotrione, 745+Mesotrione, 745+Topramezone, 745+Tembotrione, 745+Bicyclopyrone, 745+Tefuryltrione, 745+Benzobicyclon, 745+Lancotrione, 745+Shuangzuocaotong, 745+Huanbifucaotong, 745+Sanzuohuangcaotong, 745+Benzuofucaotong, 745+Pyrasulfotole, 745+Pyrazolate, 745+Benzofenap, 745+Tolpyralate, 745+Fenquinotrione, 745+Isoxaflutole, 745+Fluroxypyr or esters thereof, 745+Halauxifen-methyl, 745+Florpyrauxifen-benzyl, 745+Quinclorac, 745+Quinmerac, 745+Chipton or salts/esters thereof, 745+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 745+MCPB or salts/esters thereof, 745+2,4-D or salts/esters thereof, 745+Dichlorprop or salts/esters thereof, 745+2,4-DB or salts/esters thereof, 745+Dicamba, 745+Picloram, 745+Trichlopyr, 745+Clopyralid, 745+Triclopyr, 745+Flurochloridone, 745+Flurtamone, 745+Diflufenican, 745+Picolinafen, 745+Beflubutamid, 745+Norflurazon, 745+Fluridone.

    [0332] 746+Sulcotrione, 746+Mesotrione, 746+Topramezone, 746+Tembotrione, 746+Bicyclopyrone, 746+Tefuryltrione, 746+Benzobicyclon, 746+Lancotrione, 746+Shuangzuocaotong, 746+Huanbifucaotong, 746+Sanzuohuangcaotong, 746+Benzuofucaotong, 746+Pyrasulfotole, 746+Pyrazolate, 746+Benzofenap, 746+Tolpyralate, 746+Fenquinotrione, 746+Isoxaflutole, 746+Fluroxypyr or esters thereof, 746+Halauxifen-methyl, 746+Florpyrauxifen-benzyl, 746+Quinclorac, 746+Quinmerac, 746+Chipton or salts/esters thereof, 746+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 746+MCPB or salts/esters thereof, 746+2,4-D or salts/esters thereof, 746+Dichlorprop or salts/esters thereof, 746+2,4-DB or salts/esters thereof, 746+Dicamba, 746+Picloram, 746+Trichlopyr, 746+Clopyralid, 746+Triclopyr, 746+Flurochloridone, 746+Flurtamone, 746+Diflufenican, 746+Picolinafen, 746+Beflubutamid, 746+Norflurazon, 746+Fluridone.

    [0333] 779+Sulcotrione, 779+Mesotrione, 779+Topramezone, 779+Tembotrione, 779+Bicyclopyrone, 779+Tefuryltrione, 779+Benzobicyclon, 779+Lancotrione, 779+Shuangzuocaotong, 779+Huanbifucaotong, 779+Sanzuohuangcaotong, 779+Benzuofucaotong, 779+Pyrasulfotole, 779+Pyrazolate, 779+Benzofenap, 779+Tolpyralate, 779+Fenquinotrione, 779+Isoxaflutole, 779+Fluroxypyr or esters thereof, 779+Halauxifen-methyl, 779+Florpyrauxifen-benzyl, 779+Quinclorac, 779+Quinmerac, 779+Chipton or salts/esters thereof, 779+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 779+MCPB or salts/esters thereof, 779+2,4-D or salts/esters thereof, 779+Dichlorprop or salts/esters thereof, 779+2,4-DB or salts/esters thereof, 779+Dicamba, 779+Picloram, 779+Trichlopyr, 779+Clopyralid, 779+Triclopyr, 779+Flurochloridone, 779+Flurtamone, 779+Diflufenican, 779+Picolinafen, 779+Beflubutamid, 779+Norflurazon, 779+Fluridone.

    [0334] 963+Sulcotrione, 963+Mesotrione, 963+Topramezone, 963+Tembotrione, 963+Bicyclopyrone, 963+Tefuryltrione, 963+Benzobicyclon, 963+Lancotrione, 963+Shuangzuocaotong, 963+Huanbifucaotong, 963+Sanzuohuangcaotong, 963+Benzuofucaotong, 963+Pyrasulfotole, 963+Pyrazolate, 963+Benzofenap, 963+Tolpyralate, 963+Fenquinotrione, 963+Isoxaflutole, 963+Fluroxypyr or esters thereof, 963+Halauxifen-methyl, 963+Florpyrauxifen-benzyl, 963+Quinclorac, 963+Quinmerac, 963+Chipton or salts/esters thereof, 963+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 963+MCPB or salts/esters thereof, 963+2,4-D or salts/esters thereof, 963+Dichlorprop or salts/esters thereof, 963+2,4-DB or salts/esters thereof, 963+Dicamba, 963+Picloram, 963+Trichlopyr, 963+Clopyralid, 963+Triclopyr, 963+Flurochloridone, 963+Flurtamone, 963+Diflufenican, 963+Picolinafen, 963+Beflubutamid, 963+Norflurazon, 963+Fluridone.

    [0335] 1000+Sulcotrione, 1000+Mesotrione, 1000+Topramezone, 1000+Tembotrione, 1000+Bicyclopyrone, 1000+Tefuryltrione, 1000+Benzobicyclon, 1000+Lancotrione, 1000+Shuangzuocaotong, 1000+Huanbifucaotong, 1000+Sanzuohuangcaotong, 1000+Benzuofucaotong, 1000+Pyrasulfotole, 1000+Pyrazolate, 1000+Benzofenap, 1000+Tolpyralate, 1000+Fenquinotrione, 1000+Isoxaflutole, 1000+Fluroxypyr or esters thereof, 1000+Halauxifen-methyl, 1000+Florpyrauxifen-benzyl, 1000+Quinclorac, 1000+Quinmerac, 1000+Chipton or salts/esters thereof, 1000+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 1000+MCPB or salts/esters thereof, 1000+2,4-D or salts/esters thereof, 1000+Dichlorprop or salts/esters thereof, 1000+2,4-DB or salts/esters thereof, 1000+Dicamba, 1000+Picloram, 1000+Trichlopyr, 1000+Clopyralid, 1000+Triclopyr, 1000+Flurochloridone, 1000+Flurtamone, 1000+Diflufenican, 1000+Picolinafen, 1000+Beflubutamid, 1000+Norflurazon, 1000+Fluridone.

    [0336] 1-3+Sulcotrione, 1-3+Mesotrione, 1-3+Topramezone, 1-3+Tembotrione, 1-3+Bicyclopyrone, 1-3+Tefuryltrione, 1-3+Benzobicyclon, 1-3+Lancotrione, 1-3+Shuangzuocaotong, 1-3+Huanbifucaotong, 1-3+Sanzuohuangcaotong, 1-3+Benzuofucaotong, 1-3+Pyrasulfotole, 1-3+Pyrazolate, 1-3+Benzofenap, 1-3+Tolpyralate, 1-3+Fenquinotrione, 1-3+Isoxaflutole, 1-3+Fluroxypyr or esters thereof, 1-3+Halauxifen-methyl, 1-3+Florpyrauxifen-benzyl, 1-3+Quinclorac, 1-3+Quinmerac, 1-3+Chipton or salts/esters thereof, 1-3+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 1-3+MCPB or salts/esters thereof, 1-3+2,4-D or salts/esters thereof, 1-3+Dichlorprop or salts/esters thereof, 1-3+2,4-DB or salts/esters thereof, 1-3+Dicamba, 1-3+Picloram, 1-3+Trichlopyr, 1-3+Clopyralid, 1-3+Triclopyr, 1-3+Flurochloridone, 1-3+Flurtamone, 1-3+Diflufenican, 1-3+Picolinafen, 1-3+Beflubutamid, 1-3+Norflurazon, 1-3+Fluridone. 1-39+Sulcotrione, 1-39+Mesotrione, 1-39+Topramezone, 1-39+Tembotrione, 1-39+Bicyclopyrone, 1-39+Tefuryltrione, 1-39+Benzobicyclon, 1-39+Lancotrione, 1-39+Shuangzuocaotong, 1-39+Huanbifucaotong, 1-39+Sanzuohuangcaotong, 1-39+Benzuofucaotong, 1-39+Pyrasulfotole, 1-39+Pyrazolate, 1-39+Benzofenap, 1-39+Tolpyralate, 1-39+Fenquinotrione, 1-39+Isoxaflutole, 1-39+Fluroxypyr or esters thereof, 1-39+Halauxifen-methyl, 1-39+Florpyrauxifen-benzyl, 1-39+Quinclorac, 1-39+Quinmerac, 1-39+Chipton or salts/esters thereof, 1-39+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 1-39+MCPB or salts/esters thereof, 1-39+2,4-D or salts/esters thereof, 1-39+Dichlorprop or salts/esters thereof, 1-39+2,4-DB or salts/esters thereof, 1-39+Dicamba, 1-39+Picloram, 1-39+Trichlopyr, 1-39+Clopyralid, 1-39+Triclopyr, 1-39+Flurochloridone, 1-39+Flurtamone, 1-39+Diflufenican, 1-39+Picolinafen, 1-39+Beflubutamid, 1-39+Norflurazon, 1-39+Fluridone. 1-43+Sulcotrione, 1-43+Mesotrione, 1-43+Topramezone, 1-43+Tembotrione, 1-43+Bicyclopyrone, 1-43+Tefuryltrione, 1-43+Benzobicyclon, 1-43+Lancotrione, 1-43+Shuangzuocaotong, 1-43+Huanbifucaotong, 1-43+Sanzuohuangcaotong, 1-43+Benzuofucaotong, 1-43+Pyrasulfotole, 1-43+Pyrazolate, 1-43+Benzofenap, 1-43+Tolpyralate, 1-43+Fenquinotrione, 1-43+Isoxaflutole, 1-43+Fluroxypyr or esters thereof, 1-43+Halauxifen-methyl, 1-43+Florpyrauxifen-benzyl, 1-43+Quinclorac, 1-43+Quinmerac, 1-43+Chipton or salts/esters thereof, 1-43+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 1-43+MCPB or salts/esters thereof, 1-43+2,4-D or salts/esters thereof, 1-43+Dichlorprop or salts/esters thereof, 1-43+2,4-DB or salts/esters thereof, 1-43+Dicamba, 1-43+Picloram, 1-43+Trichlopyr, 1-43+Clopyralid, 1-43+Triclopyr, 1-43+Flurochloridone, 1-43+Flurtamone, 1-43+Diflufenican, 1-43+Picolinafen, 1-43+Beflubutamid, 1-43+Norflurazon, 1-43+Fluridone.

    [0337] 1-55+Sulcotrione, 1-55+Mesotrione, 1-55+Topramezone, 1-55+Tembotrione, 1-55+Bicyclopyrone, 1-55+Tefuryltrione, 1-55+Benzobicyclon, 1-55+Lancotrione, 1-55+Shuangzuocaotong, 1-55+Huanbifucaotong, 1-55+Sanzuohuangcaotong, 1-55+Benzuofucaotong, 1-55+Pyrasulfotole, 1-55+Pyrazolate, 1-55+Benzofenap, 1-55+Tolpyralate, 1-55+Fenquinotrione, 1-55+Isoxaflutole, 1-55+Fluroxypyr or esters thereof, 1-55+Halauxifen-methyl, 1-55+Florpyrauxifen-benzyl, 1-55+Quinclorac, 1-55+Quinmerac, 1-55+Chipton or salts/esters thereof, 1-55+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 1-55+MCPB or salts/esters thereof, 1-55+2,4-D or salts/esters thereof, 1-55+Dichlorprop or salts/esters thereof, 1-55+2,4-DB or salts/esters thereof, 1-55+Dicamba, 1-55+Picloram, 1-55+Trichlopyr, 1-55+Clopyralid, 1-55+Triclopyr, 1-55+Flurochloridone, 1-55+Flurtamone, 1-55+Diflufenican, 1-55+Picolinafen, 1-55+Beflubutamid, 1-55+Norflurazon, 1-55+Fluridone.

    [0338] 1-82+Sulcotrione, 1-82+Mesotrione, 1-82+Topramezone, 1-82+Tembotrione, 1-82+Bicyclopyrone, 1-82+Tefuryltrione, 1-82+Benzobicyclon, 1-82+Lancotrione, 1-82+Shuangzuocaotong, 1-82+Huanbifucaotong, 1-82+Sanzuohuangcaotong, 1-82+Benzuofucaotong, 1-82+Pyrasulfotole, 1-82+Pyrazolate, 1-82+Benzofenap, 1-82+Tolpyralate, 1-82+Fenquinotrione, 1-82+Isoxaflutole, 1-82+Fluroxypyr or esters thereof, 1-82+Halauxifen-methyl, 1-82+Florpyrauxifen-benzyl, 1-82+Quinclorac, 1-82+Quinmerac, 1-82+Chipton or salts/esters thereof, 1-82+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 1-82+MCPB or salts/esters thereof, 1-82+2,4-D or salts/esters thereof, 1-82+Dichlorprop or salts/esters thereof, 1-82+2,4-DB or salts/esters thereof, 1-82+Dicamba, 1-82+Picloram, 1-82+Trichlopyr, 1-82+Clopyralid, 1-82+Triclopyr, 1-82+Flurochloridone, 1-82+Flurtamone, 1-82+Diflufenican, 1-82+Picolinafen, 1-82+Beflubutamid, 1-82+Norflurazon, 1-82+Fluridone.

    [0339] 1-86+Sulcotrione, 1-86+Mesotrione, 1-86+Topramezone, 1-86+Tembotrione, 1-86+Bicyclopyrone, 1-86+Tefuryltrione, 1-86+Benzobicyclon, 1-86+Lancotrione, 1-86+Shuangzuocaotong, 1-86+Huanbifucaotong, 1-86+Sanzuohuangcaotong, 1-86+Benzuofucaotong, 1-86+Pyrasulfotole, 1-86+Pyrazolate, 1-86+Benzofenap, 1-86+Tolpyralate, 1-86+Fenquinotrione, 1-86+Isoxaflutole, 1-86+Fluroxypyr or esters thereof, 1-86+Halauxifen-methyl, 1-86+Florpyrauxifen-benzyl, 1-86+Quinclorac, 1-86+Quinmerac, 1-86+Chipton or salts/esters thereof, 1-86+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 1-86+MCPB or salts/esters thereof, 1-86+2,4-D or salts/esters thereof, 1-86+Dichlorprop or salts/esters thereof, 1-86+2,4-DB or salts/esters thereof, 1-86+Dicamba, 1-86+Picloram, 1-86+Trichlopyr, 1-86+Clopyralid, 1-86+Triclopyr, 1-86+Flurochloridone, 1-86+Flurtamone, 1-86+Diflufenican, 1-86+Picolinafen, 1-86+Beflubutamid, 1-86+Norflurazon, 1-86+Fluridone.

    [0340] 1-226+Sulcotrione, 1-226+Mesotrione, 1-226+Topramezone, 1-226+Tembotrione, 1-226+Bicyclopyrone, 1-226+Tefuryltrione, 1-226+Benzobicyclon, 1-226+Lancotrione, 1-226+Shuangzuocaotong, 1-226+Huanbifucaotong, 1-226+Sanzuohuangcaotong, 1-226+Benzuofucaotong, 1-226+Pyrasulfotole, 1-226+Pyrazolate, 1-226+Benzofenap, 1-226+Tolpyralate, 1-226+Fenquinotrione, 1-226+Isoxaflutole, 1-226+Fluroxypyr or esters thereof, 1-226+Halauxifen-methyl, 1-226+Florpyrauxifen-benzyl, 1-226+Quinclorac, 1-226+Quinmerac, 1-226+Chipton or salts/esters thereof, 1-226+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 1-226+MCPB or salts/esters thereof, 1-226+2,4-D or salts/esters thereof, 1-226+Dichlorprop or salts/esters thereof, 1-226+2,4-DB or salts/esters thereof, 1-226+Dicamba, 1-226+Picloram, 1-226+Trichlopyr, 1-226+Clopyralid, 1-226+Triclopyr, 1-226+Flurochloridone, 1-226+Flurtamone, 1-226+Diflufenican, 1-226+Picolinafen, 1-226+Beflubutamid, 1-226+Norflurazon, 1-226+Fluridone.

    [0341] 1-227+Sulcotrione, 1-227+Mesotrione, 1-227+Topramezone, 1-227+Tembotrione, 1-227+Bicyclopyrone, 1-227+Tefuryltrione, 1-227+Benzobicyclon, 1-227+Lancotrione, 1-227+Shuangzuocaotong, 1-227+Huanbifucaotong, 1-227+Sanzuohuangcaotong, 1-227+Benzuofucaotong, 1-227+Pyrasulfotole, 1-227+Pyrazolate, 1-227+Benzofenap, 1-227+Tolpyralate, 1-227+Fenquinotrione, 1-227+Isoxaflutole, 1-227+Fluroxypyr or esters thereof, 1-227+Halauxifen-methyl, 1-227+Florpyrauxifen-benzyl, 1-227+Quinclorac, 1-227+Quinmerac, 1-227+Chipton or salts/esters thereof, 1-227+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 1-227+MCPB or salts/esters thereof, 1-227+2,4-D or salts/esters thereof, 1-227+Dichlorprop or salts/esters thereof, 1-227+2,4-DB or salts/esters thereof, 1-227+Dicamba, 1-227+Picloram, 1-227+Trichlopyr, 1-227+Clopyralid, 1-227+Triclopyr, 1-227+Flurochloridone, 1-227+Flurtamone, 1-227+Diflufenican, 1-227+Picolinafen, 1-227+Beflubutamid, 1-227+Norflurazon, 1-227+Fluridone.

    [0342] 1-228+Sulcotrione, 1-228+Mesotrione, 1-228+Topramezone, 1-228+Tembotrione, 1-228+Bicyclopyrone, 1-228+Tefuryltrione, 1-228+Benzobicyclon, 1-228+Lancotrione, 1-228+Shuangzuocaotong, 1-228+Huanbifucaotong, 1-228+Sanzuohuangcaotong, 1-228+Benzuofucaotong, 1-228+Pyrasulfotole, 1-228+Pyrazolate, 1-228+Benzofenap, 1-228+Tolpyralate, 1-228+Fenquinotrione, 1-228+Isoxaflutole, 1-228+Fluroxypyr or esters thereof, 1-228+Halauxifen-methyl, 1-228+Florpyrauxifen-benzyl, 1-228+Quinclorac, 1-228+Quinmerac, 1-228+Chipton or salts/esters thereof, 1-228+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 1-228+MCPB or salts/esters thereof, 1-228+2,4-D or salts/esters thereof, 1-228+Dichlorprop or salts/esters thereof, 1-228+2,4-DB or salts/esters thereof, 1-228+Dicamba, 1-228+Picloram, 1-228+Trichlopyr, 1-228+Clopyralid, 1-228+Triclopyr, 1-228+Flurochloridone, 1-228+Flurtamone, 1-228+Diflufenican, 1-228+Picolinafen, 1-228+Beflubutamid, 1-228+Norflurazon, 1-228+Fluridone.

    [0343] 1-229+Sulcotrione, 1-229+Mesotrione, 1-229+Topramezone, 1-229+Tembotrione, 1-229+Bicyclopyrone, 1-229+Tefuryltrione, 1-229+Benzobicyclon, 1-229+Lancotrione, 1-229+Shuangzuocaotong, 1-229+Huanbifucaotong, 1-229+Sanzuohuangcaotong, 1-229+Benzuofucaotong, 1-229+Pyrasulfotole, 1-229+Pyrazolate, 1-229+Benzofenap, 1-229+Tolpyralate, 1-229+Fenquinotrione, 1-229+Isoxaflutole, 1-229+Fluroxypyr or esters thereof, 1-229+Halauxifen-methyl, 1-229+Florpyrauxifen-benzyl, 1-229+Quinclorac, 1-229+Quinmerac, 1-229+Chipton or salts/esters thereof, 1-229+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 1-229+MCPB or salts/esters thereof, 1-229+2,4-D or salts/esters thereof, 1-229+Dichlorprop or salts/esters thereof, 1-229+2,4-DB or salts/esters thereof, 1-229+Dicamba, 1-229+Picloram, 1-229+Trichlopyr, 1-229+Clopyralid, 1-229+Triclopyr, 1-229+Flurochloridone, 1-229+Flurtamone, 1-229+Diflufenican, 1-229+Picolinafen, 1-229+Beflubutamid, 1-229+Norflurazon, 1-229+Fluridone.

    [0344] 1-230+Sulcotrione, 1-230+Mesotrione, 1-230+Topramezone, 1-230+Tembotrione, 1-230+Bicyclopyrone, 1-230+Tefuryltrione, 1-230+Benzobicyclon, 1-230+Lancotrione, 1-230+Shuangzuocaotong, 1-230+Huanbifucaotong, 1-230+Sanzuohuangcaotong, 1-230+Benzuofucaotong, 1-230+Pyrasulfotole, 1-230+Pyrazolate, 1-230+Benzofenap, 1-230+Tolpyralate, 1-230+Fenquinotrione, 1-230+Isoxaflutole, 1-230+Fluroxypyr or esters thereof, 1-230+Halauxifen-methyl, 1-230+Florpyrauxifen-benzyl, 1-230+Quinclorac, 1-230+Quinmerac, 1-230+Chipton or salts/esters thereof, 1-230+2-methyl 4-chlorophenoxypropionic acid or salts/esters thereof, 1-230+MCPB or salts/esters thereof, 1-230+2,4-D or salts/esters thereof, 1-230+Dichlorprop or salts/esters thereof, 1-230+2,4-DB or salts/esters thereof, 1-230+Dicamba, 1-230+Picloram, 1-230+Trichlopyr, 1-230+Clopyralid, 1-230+Triclopyr, 1-230+Flurochloridone, 1-230+Flurtamone, 1-230+Diflufenican, 1-230+Picolinafen, 1-230+Beflubutamid, 1-230+Norflurazon, 1-230+Fluridone.

    [0345] Wherein, the actual control effect of the combination of the above components (i) and (ii) on weeds were tested with postemergence applicaitons, that is, when the weeds were in the 3-4 leaf stage, the combination mentioned above diluted with 30 kg/667 m.sup.2 water were sprayed uniformly to the stems and leaves of the weed by the hand sprayer. 20 days after treatment, Theoretical fresh weight inhibition rate of a combination of two active ingredients in each group was calculated by the Cowing method (E0=X+Y−X*Y/100), and then compared with an actually measured inhibition rate (E), thereby effect of the combination (hereafter referred to as combined effect) on weeds was evaluated: the value of E−E0, which was greater than 10%, corresponded to a synergistic effect, the value of E−E0, which was less than −10%, corresponded to an antagonistic effect, and the value of E−E0, which was from −10% to 10%, corresponded to an additional effect. An optimum ratio of the two active ingredients was determined by the actual control effect, characteristics of herbicides, and balance of a corresponding formula. Wherein, in the formula, X represented the fresh weight inhibition rate of the active ingredient A in a dosage of P, and Y represented the fresh weight inhibition rate of the active ingredient B in a dosage of Q. The statistic results are shown in Table 6.

    TABLE-US-00006 TABLE 6 Actual control effect and synergistic effect of the mixture of (i) and (ii) in weeds (Gowing method) Inhibitory Inhibitory effect of effect of component (i) component (ii) when applied when applied Component (i)/ (i) + (ii) Weed alone at alone at E E0 E − E0 Compound No. Component (ii) g a.i./ha species same dose same dose (%) (%) (%) (%) 1 Sulcotrione 30 + 50 Abutilon 20 30 100 44 56 theophrasti 1 Mesotrione 30 + 30 Abutilon 20 40 100 52 48 theophrasti 1 Topramezone 30 + 5  Abutilon 20 40 100 52 48 theophrasti 1 Tembotrione 30 + 15 Abutilon 20 30 100 44 56 theophrasti 1 Bicyclopyrone 30 + 15 Abutilon 20 40 100 52 48 theophrasti 1 Tefuryltrione 30 + 50 Abutilon 20 40 80 52 28 theophrasti 1 Benzobicyclon  30 + 150 Abutilon 20 50 100 60 40 theophrasti 1 Lancotrione 30 + 50 Abutilon 20 40 100 52 48 theophrasti 1 Shuangzuocaotong 30 + 5  Sisymbrium 20 40 100 52 48 sophia 1 Huanbifucaotong 30 + 30 Abutilon 20 30 100 44 56 theophrasti 1 Sanzuohuangcaotong 30 + 30 Abutilon 20 30 100 44 56 theophrasti 1 Benzuofucaotong 30 + 15 Abutilon 20 40 100 52 48 theophrasti 1 Pyrasulfotole 30 + 15 Abutilon 20 50 100 60 40 theophrasti 1 Benzofenap  30 + 150 Abutilon 20 40 100 52 48 theophrasti 1 Tolpyralate 30 + 5  Abutilon 20 50 100 60 40 theophrasti 1 Isoxaflutole 30 + 30 Abutilon 20 30 100 44 56 theophrasti 1 Fluroxypyr 30 + 30 Galium 20 40 80 52 28 aparine 1 Halauxifen- 30 + 2  Abutilon 20 40 100 52 48 methyl theophrasti 1 Florpyrauxifen- 30 + 2  Abutilon 20 45 100 56 44 benzyl theophrasti 1 Quinclorac 30 + 50 Galium 20 50 80 60 20 aparine 1 Chipton 30 + 60 Sisymbrium 20 40 80 52 28 sodium salt sophia 1 2-methyl 4-  30 + 100 Sisymbrium 20 30 75 44 31 chlorophenoxy sophia propionic acid 1 MCPB  30 + 200 Sisymbrium 20 40 85 52 33 sophia 1 2,4-D iso-octyl 30 + 50 Sisymbrium 20 40 85 52 33 ester sophia 1 Dichlorprop  30 + 100 Sisymbrium 20 40 100 52 48 sophia 1 2,4-DB  30 + 200 Sisymbrium 20 50 90 60 30 sophia 1 Dicamba 30 + 10 Sisymbrium 20 30 75 44 31 sophia 1 Picloram 30 + 50 Abutilon 20 40 80 52 28 theophrasti 1 Trichlopyr 30 + 50 Abutilon 20 40 70 52 18 theophrasti 1 Clopyralid 30 + 50 Galinsoga 30 40 85 58 27 parviflora 1 Triclopyr 30 + 50 Abutilon 20 35 75 48 27 theophrasti 1 Flurochloridone  30 + 100 Galium 20 40 90 52 38 aparine 1 Flurtamone  30 + 100 Galium 20 35 85 48 37 aparine 1 Diflufenican  30 + 100 Veronica 30 45 90 61.5 28.5 polita 1 Picolinafen 30 + 50 Abutilon 20 30 85 44 41 theophrasti 1 Beflubutamid  30 + 200 Abutilon 20 40 100 52 48 theophrasti 1 Norflurazon  30 + 300 Abutilon 20 50 85 60 25 theophrasti 1 Fluridone  30 + 100 Abutilon 20 45 85 56 29 theophrasti

    [0346] At the same time, it is found after several tests that similar herbicidal effects were achieved when other components (i) of the present invention were combined with the component (ii). In addition, the compound and the composition of the present invention have good selectivity to many gramineae grasses such as zoysia japonica, Bermuda grass, tall fescue, bluegrass, ryegrass and seashore paspalum etc, and are able to control many important grass weeds and broadleaf weeds. The compounds also show excellent selectivity and commercial value in the tests on wheat, corn, rice, sugarcane, soybean, cotton, oil sunflower, potato, orchards and vegetables in different herbicide application methods.