1. Patent Search
  2. Details

Novel isothiazolamides, processes for their preparation and their use as herbicides and/or plant growth regulators

20190037848 · 2019-02-07

    Inventors

    Cpc classification

    International classification

    Abstract

    The invention relates to the technical field of the herbicides and/or plant growth regulators. Specifically, the invention primarily relates to novel isothiazolamides, and compositions comprising said novel isothiazolamides. Further, the present invention relates to processes for the preparation said novel isothiazolamides and their use as herbicides and/or plant growth regulators.

    Claims

    1. A product comprising one or more compounds of formula (G) and/or one or more salts thereof, ##STR00023## in which A is CR.sup.6R.sup.7, W is O or S, R.sup.1 is hydrogen, (C.sub.1-C.sub.12)-alkyl, (C.sub.1-C.sub.12)-haloalkyl, (C.sub.2-C.sub.12)-alkenyl, (C.sub.2-C.sub.12)-haloalkenyl, (C.sub.2-C.sub.12)-alkynyl, (C.sub.2-C.sub.12)-haloalkynyl, NR.sup.13R.sup.14, R.sup.13R.sup.14N(C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.6)-alkoxy, (C.sub.1-C.sub.6)-haloalkoxy, (C.sub.1-C.sub.6)-haloalkoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.6)-alkoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.6)-alkoxy-(C.sub.2-C.sub.6)-alkoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, (C.sub.1-C.sub.4)-haloalkylthio, (C.sub.1-C.sub.4)-haloalkylsulphoxy, (C.sub.1-C.sub.4)-haloalkylsulphonyl, (C.sub.1-C.sub.4)-alkylthio-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylsulphoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylsulphonyl-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-haloalkylthio-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-haloalkylsulphoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-haloalkylsulphonyl-(C.sub.1-C.sub.3)-alkyl, (C.sub.3-C.sub.12)-cycloalkyl, (C.sub.3-C.sub.8)-cycloalkenyl, (C.sub.3-C.sub.12)-cycloalkyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.3-C.sub.8)-cycloalkenyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.3-C.sub.8)-cycloalkoxy, (C.sub.3-C.sub.8)-cycloalkyl-(C.sub.1-C.sub.6)-alkoxy, aryl, aryl-(C.sub.1-C.sub.3)-alkyl, heteroaryl, heteroaryl-(C.sub.1-C.sub.3)-alkyl, heterocyclyl, heterocyclyl-(C.sub.1-C.sub.3)-alkyl, aryloxy, heteroaryloxy, heterocyclyloxy, a bicyclic or a heterobicyclic residue, wherein each of the last-mentioned 17 residues is unsubstituted or is substituted by one or more residues from the group consisting of halogen, nitro, hydroxyl, cyano, NR.sup.13R.sup.14, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, (C.sub.1-C.sub.4)-haloalkylthio, (C.sub.1-C.sub.4)-haloalkylsulphoxy, (C.sub.1-C.sub.4)-haloalkylsulphonyl, (C.sub.1-C.sub.4)-alkoxycarbonyl, (C.sub.1-C.sub.4)-haloalkoxycarbonyl, (C.sub.1-C.sub.4)-alkylcarboxy, (C.sub.3-C.sub.6)-cycloalkyl, (C.sub.3-C.sub.6)-cycloalkyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.4)-alkoxycarbonyl-(C.sub.1-C.sub.4)-alkyl, hydroxycarbonyl, hydroxycarbonyl-(C.sub.1-C.sub.4)-alkyl, R.sup.13R.sup.14N-carbonyl, and wherein heterocyclyl has q oxo groups, and wherein each of the aforementioned heterocyclic residues, in addition to the carbon atoms, has in each case p ring members from the group consisting of N(R.sup.12).sub.m, O and S(O).sub.n, R.sup.2 is hydrogen, (C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.6)-haloalkyl, (C.sub.2-C.sub.6)-alkenyl, (C.sub.2-C.sub.6)-haloalkenyl, (C.sub.2-C.sub.6)-alkynyl, (C.sub.2-C.sub.6)-haloalkynyl, (C.sub.1-C.sub.4)-alkylsulphonyl, (C.sub.1-C.sub.4)-haloalkylsulphonyl, (C.sub.1-C.sub.6)-alkylcarbonyl, (C.sub.2-C.sub.6)-alkenylcarbonyl, (C.sub.2-C.sub.6)-alkynylcarbonyl, (C.sub.1-C.sub.6)-haloalkylcarbonyl, (C.sub.2-C.sub.6)-haloalkenylcarbonyl, (C.sub.2-C.sub.6)-haloalkynylcarbonyl, (C.sub.1-C.sub.6)-alkoxycarbonyl, di((C.sub.1-C.sub.6)-alkyl)aminocarbonyl, (C.sub.3-C.sub.8)-cycloalkyl, (C.sub.3-C.sub.8)-cycloalkyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.3-C.sub.8)-cycloalkylcarbonyl, (C.sub.3-C.sub.8)-cycloalkyl-(C.sub.1-C.sub.6)-alkylcarbonyl, heteroarylcarbonyl, or arylcarbonyl, wherein each of the last-mentioned 6 residues is unsubstituted or is substituted by one or more residues from the group consisting of halogen, nitro, hydroxyl, cyano, NR.sup.13R.sup.14, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, (C.sub.1-C.sub.4)-haloalkylthio, (C.sub.1-C.sub.4)-haloalkylsulphoxy, (C.sub.1-C.sub.4)-haloalkylsulphonyl, (C.sub.1-C.sub.4)-alkoxycarbonyl, (C.sub.1-C.sub.4)-haloalkoxycarbonyl, (C.sub.1-C.sub.4)-alkylcarboxy, (C.sub.3-C.sub.6)-cycloalkyl, (C.sub.3-C.sub.6)-cycloalkyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.4)-alkoxycarbonyl-(C.sub.1-C.sub.4)-alkyl, hydroxycarbonyl, hydroxycarbonyl-(C.sub.1-C.sub.4)-alkyl, R.sup.13R.sup.14N-carbonyl, or R.sup.1 and R.sup.2, together with the nitrogen atom and (A).sub.y attached thereto, form a 5- or 6-membered heterocyclic or heteroaromatic ring, which comprises in each case, in addition to the carbon atoms and the nitrogen atom, p ring members from the group consisting of N(R.sup.12).sub.m, O and S(O).sub.n and wherein said ring is unsubstituted or is substituted by one or more residues from the group consisting of halogen, nitro, hydroxyl, cyano, NR.sup.13R.sup.14, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, (C.sub.1-C.sub.4)-haloalkylthio, (C.sub.1-C.sub.4)-haloalkylsulphoxy, (C.sub.1-C.sub.4)-haloalkylsulphonyl, (C.sub.1-C.sub.4)-alkoxycarbonyl, (C.sub.1-C.sub.4)-haloalkoxycarbonyl, (C.sub.1-C.sub.4)-alkylcarboxy, (C.sub.3-C.sub.6)-cycloalkyl, (C.sub.3-C.sub.6)-cycloalkyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.4)-alkoxycarbonyl-(C.sub.1-C.sub.4)-alkyl, hydroxycarbonyl, hydroxycarbonyl-(C.sub.1-C.sub.4)-alkyl, R.sup.13R.sup.14N-carbonyl and has q oxo groups, R.sup.3 is hydrogen, halogen, azido, isocyanate, isothiocyanate, nitro, cyano, hydroxyl, NR.sup.13R.sup.14, tri(C.sub.1-C.sub.6)-alkylsilyl, (C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.6)-haloalkyl, (C.sub.2-C.sub.6)-alkenyl, (C.sub.2-C.sub.6)-haloalkenyl, (C.sub.2-C.sub.6)-alkynyl, (C.sub.2-C.sub.6)-haloalkynyl, (C.sub.1-C.sub.6)-alkoxy, (C.sub.1-C.sub.6)-haloalkoxy, (C.sub.1-C.sub.6)-haloalkoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.6)-alkoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.6)-alkoxy-(C.sub.2-C.sub.6)-alkoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.6)-alkylcarbonyloxy, (C.sub.1-C.sub.6)-haloalkylcarbonyloxy, (C.sub.2-C.sub.6)-alkenylcarbonyloxy, (C.sub.2-C.sub.6)-alkynylcarbonyloxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, (C.sub.1-C.sub.4)-haloalkylthio, (C.sub.1-C.sub.4)-haloalkylsulphoxy, (C.sub.1-C.sub.4)-haloalkylsulphonyl, (C.sub.1-C.sub.4)-alkylthio-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylsulphoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylsulphonyl-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-haloalkylthio-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-haloalkylsulphoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-haloalkylsulphonyl-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.6)-alkoxycarbonyl, (C.sub.1-C.sub.6)-haloalkoxycarbonyl, (C.sub.2-C.sub.6)-alkenyloxycarbonyl, (C.sub.2-C.sub.6)-haloalkenyloxycarbonyl, (C.sub.2-C.sub.6)-alkynyloxycarbonyl, (C.sub.2-C.sub.6)-haloalkynyloxycarbonyl, (C.sub.1-C.sub.6)-alkylcarbonyl, (C.sub.1-C.sub.6)-haloalkylcarbonyl, (C.sub.2-C.sub.6)-alkenylcarbonyl, (C.sub.2-C.sub.6)-haloalkenylcarbonyl, (C.sub.2-C.sub.6)-alkynylcarbonyl, (C.sub.2-C.sub.6)-haloalkynylcarbonyl, R.sup.13R.sup.14N-carbonyl, arylthio, arylsulphoxy, arylsulphonyl, (C.sub.3-C.sub.8)-cycloalkyl, (C.sub.3-C.sub.8)-cycloalkenyl, (C.sub.3-C.sub.8)-cycloalkyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.3-C.sub.8)-cycloalkenyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.3-C.sub.8)-cycloalkoxy, aryl, aryloxy, arylcarbonyloxy, aryl-(C.sub.1-C.sub.3)-alkyl, heteroaryl, heteroaryloxy, heteroaryl-(C.sub.1-C.sub.3)-alkyl, heterocyclyl, heterocyclyloxy, or heterocyclyl-(C.sub.1-C.sub.3)-alkyl, wherein each of the last-mentioned 18 residues is unsubstituted or is substituted by one or more residues from the group consisting of halogen, nitro, hydroxyl, cyano, NR.sup.13R.sup.14, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, (C.sub.1-C.sub.4)-haloalkylthio, (C.sub.1-C.sub.4)-haloalkylsulphoxy, (C.sub.1-C.sub.4)-haloalkylsulphonyl, (C.sub.1-C.sub.4)-alkoxycarbonyl, (C.sub.1-C.sub.4)-haloalkoxycarbonyl, (C.sub.1-C.sub.4)-alkylcarboxy, (C.sub.3-C.sub.6)-cycloalkyl, (C.sub.3-C.sub.6)-cycloalkyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.4)-alkoxycarbonyl-(C.sub.1-C.sub.4)-alkyl, hydroxycarbonyl, hydroxycarbonyl-(C.sub.1-C.sub.4)-alkyl, R.sup.13R.sup.14N-carbonyl, and wherein heterocyclyl has q oxo groups, R.sup.4, R.sup.5 are each independently hydrogen, (C.sub.1-C.sub.12)-alkyl, (C.sub.1-C.sub.12)-haloalkyl, (C.sub.2-C.sub.12)-alkenyl, (C.sub.2-C.sub.12)-haloalkenyl, (C.sub.2-C.sub.12)-alkynyl, (C.sub.2-C.sub.12)-haloalkynyl, (C.sub.1-C.sub.6)-alkoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.6)-alkoxy-(C.sub.2-C.sub.6)-alkoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.6)-alkoxy-(C.sub.1-C.sub.3)-alkylcarbonyl, (C.sub.1-C.sub.6)-alkoxy-(C.sub.2-C.sub.6)-alkoxy-(C.sub.1-C.sub.3)-alkylcarbonyl, (C.sub.1-C.sub.6)-alkoxycarbonyl, (C.sub.1-C.sub.6)-haloalkoxycarbonyl, (C.sub.2-C.sub.6)-alkenyloxycarbonyl, (C.sub.2-C.sub.6)-haloalkenyloxycarbonyl, (C.sub.2-C.sub.6)-alkynyloxycarbonyl, (C.sub.2-C.sub.6)-haloalkynyloxycarbonyl, (C.sub.1-C.sub.6)-alkylcarbonyl, (C.sub.1-C.sub.6)-haloalkylcarbonyl, (C.sub.2-C.sub.6)-alkenylcarbonyl, (C.sub.2-C.sub.6)-haloalkenylcarbonyl, (C.sub.2-C.sub.6)-alkynylcarbonyl, (C.sub.2-C.sub.6)-haloalkynylcarbonyl, R.sup.13R.sup.14N-carbonyl, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-haloalkylthio, (C.sub.1-C.sub.8)-alkylthiocarbonyl, haloalkylthiocarbonyl, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-haloalkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, (C.sub.1-C.sub.4)-haloalkylsulphonyl, (C.sub.1-C.sub.4)-alkylthio-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylsulphoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylsulphonyl-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylthio-(C.sub.1-C.sub.3)-alkylcarbonyl, (C.sub.1-C.sub.4)-alkylsulphoxy-(C.sub.1-C.sub.3)-alkylcarbonyl, (C.sub.1-C.sub.4)-alkylsulphonyl-(C.sub.1-C.sub.3)-alkylcarbonyl, (C.sub.1-C.sub.12)-alkylcarbonyl, (C.sub.1-C.sub.12)-haloalkylcarbonyl, (C.sub.2-C.sub.12)-alkenylcarbonyl, (C.sub.2-C.sub.12)-haloalkenylcarbonyl, (C.sub.2-C.sub.12)-alkynylcarbonyl, (C.sub.2-C.sub.12)-haloalkynylcarbonyl, (C.sub.1-C.sub.12)-alkoxycarbonylcarbonyl, (C.sub.1-C.sub.12)-alkoxycarbonyl-(C.sub.1-C.sub.3)-alkylcarbonyl, (C.sub.3-C.sub.8)-cycloalkyl, (C.sub.3-C.sub.8)-cycloalkenyl, (C.sub.3-C.sub.8)-cycloalkyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.3-C.sub.8)-cycloalkenyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.3-C.sub.8)-cycloalkylcarbonyl, (C.sub.3-C.sub.8)-cycloalkenylcarbonyl, (C.sub.3-C.sub.8)-cycloalkyl-(C.sub.1-C.sub.6)-alkylcarbonyl, (C.sub.3-C.sub.8)-cycloalkenyl-(C.sub.1-C.sub.6)-alkylcarbonyl, aryl, aryl-(C.sub.1-C.sub.3)-alkyl, heteroaryl, heteroaryl-(C.sub.1-C.sub.3)-alkyl, heterocyclyl, heterocyclyl-(C.sub.1-C.sub.3)-alkyl, arylcarbonyl, aryl-(C.sub.1-C.sub.6)-alkylcarbonyl, heteroarylcarbonyl, heteroaryl-(C.sub.1-C.sub.6)-alkylcarbonyl, heterocyclylcarbonyl, or heterocyclyl-(C.sub.1-C.sub.6)-alkylcarbonyl, wherein each of the last-mentioned 20 residues is unsubstituted or is substituted by one or more residues from the group consisting of halogen, nitro, hydroxyl, cyano, NR.sup.13R.sup.14, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, (C.sub.1-C.sub.4)-haloalkylthio, (C.sub.1-C.sub.4)-haloalkylsulphoxy, (C.sub.1-C.sub.4)-haloalkylsulphonyl, (C.sub.1-C.sub.4)-alkoxycarbonyl, (C.sub.1-C.sub.4)-haloalkoxycarbonyl, (C.sub.1-C.sub.4)-alkylcarboxy, (C.sub.3-C.sub.6)-cycloalkyl, (C.sub.3-C.sub.6)-cycloalkyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.4)-alkoxycarbonyl-(C.sub.1-C.sub.4)-alkyl, hydroxycarbonyl, hydroxycarbonyl-(C.sub.1-C.sub.4)-alkyl, R.sup.13R.sup.14N-carbonyl, and wherein heterocyclyl has q oxo groups, wherein R.sup.4 and R.sup.5 are not both an alkyl residue, or NR.sup.4R.sup.5 is NCR.sup.8R.sup.9 or NS(O).sub.nR.sup.10R.sup.11, R.sup.6, R.sup.7 are each independently hydrogen, cyano, halogen, (C.sub.1-C.sub.6)-alkyl, (C.sub.2-C.sub.6)-alkenyl, (C.sub.2-C.sub.6)-alkynyl, or (C.sub.3-C.sub.8)-cycloalkyl, or R.sup.6 and R.sup.7, together with the carbon atom to which they are attached, form a 3-6-membered carbocyclic or heterocyclic ring, which comprises in each case, in addition to the carbon atoms, p ring members from the group consisting of N(R.sup.12).sub.m, O and S(O).sub.n and wherein said ring is unsubstituted or is substituted by one or more residues from the group consisting of halogen, nitro, hydroxyl, cyano, NR.sup.13R.sup.14, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, (C.sub.1-C.sub.4)-haloalkylthio, (C.sub.1-C.sub.4)-haloalkylsulphoxy, (C.sub.1-C.sub.4)-haloalkylsulphonyl, (C.sub.1-C.sub.4)-alkoxycarbonyl, (C.sub.1-C.sub.4)-haloalkoxycarbonyl, (C.sub.1-C.sub.4)-alkylcarboxy, (C.sub.3-C.sub.6)-cycloalkyl, (C.sub.3-C.sub.6)-cycloalkyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.4)-alkoxycarbonyl-(C.sub.1-C.sub.4)-alkyl, hydroxycarbonyl, hydroxycarbonyl-(C.sub.1-C.sub.4)-alkyl, R.sup.13R.sup.14N-carbonyl and has q oxo groups, R.sup.8, R.sup.9 are each independently hydrogen, (C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.6)-haloalkyl, (C.sub.2-C.sub.6)-alkenyl, (C.sub.2-C.sub.6)-haloalkenyl, (C.sub.2-C.sub.6)-alkynyl, (C.sub.2-C.sub.6)-haloalkynyl, (C.sub.1-C.sub.6)-alkoxy, (C.sub.1-C.sub.6)-haloalkoxy, (C.sub.1-C.sub.6)-haloalkoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.2-C.sub.6)-alkenyloxy, (C.sub.2-C.sub.6)-haloalkenyloxy, (C.sub.2-C.sub.6)-alkynyloxy, (C.sub.2-C.sub.6)-haloalkynyloxy, NR.sup.13R.sup.14, (C.sub.1-C.sub.6)-alkoxy-(C.sub.1-C.sub.3)-alkyl, halogen-(C.sub.1-C.sub.6)-alkoxy-(C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.6)-alkoxy-(C.sub.2-C.sub.6)-alkoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylthio-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylsulphoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylsulphonyl-(C.sub.1-C.sub.3)-alkyl, (C.sub.3-C.sub.8)-cycloalkyl, (C.sub.3-C.sub.8)-cycloalkenyl, (C.sub.3-C.sub.8)-cycloalkyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.3-C.sub.8)-cycloalkenyl-(C.sub.1-C.sub.6)-alkyl, aryl, aryl-(C.sub.1-C.sub.3)-alkyl, heteroaryl, heteroaryl-(C.sub.1-C.sub.3)-alkyl, heterocyclyl, heterocyclyl-(C.sub.1-C.sub.3)-alkyl, wherein each of the last-mentioned 10 residues is unsubstituted or is substituted by one or more residues from the group consisting of halogen, nitro, hydroxyl, cyano, NR.sup.13R.sup.14, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, (C.sub.1-C.sub.4)-haloalkylthio, (C.sub.1-C.sub.4)-haloalkylsulphoxy, (C.sub.1-C.sub.4)-haloalkylsulphonyl, (C.sub.1-C.sub.4)-alkoxycarbonyl, (C.sub.1-C.sub.4)-haloalkoxycarbonyl, (C.sub.1-C.sub.4)-alkylcarboxy, (C.sub.3-C.sub.6)-cycloalkyl, (C.sub.3-C.sub.6)-cycloalkyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.4)-alkoxycarbonyl-(C.sub.1-C.sub.4)-alkyl, hydroxycarbonyl, hydroxycarbonyl-(C.sub.1-C.sub.4)-alkyl, R.sup.13R.sup.14N-carbonyl and has q oxo groups, or R.sup.8 and R.sup.9, together with the carbon atom to which they are attached, form a 3- to 8-membered unsaturated, partially saturated or saturated ring, which comprises in each case, in addition to the carbon atoms, p ring members from the group consisting of N(R.sup.12).sub.m, O and S(O).sub.n and wherein said ring is unsubstituted or is substituted by one or more residues from the group consisting of halogen, nitro, hydroxyl, cyano, NR.sup.13R.sup.14, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, (C.sub.1-C.sub.4)-haloalkylthio, (C.sub.1-C.sub.4)-haloalkylsulphoxy, (C.sub.1-C.sub.4)-haloalkylsulphonyl, (C.sub.1-C.sub.4)-alkoxycarbonyl, (C.sub.1-C.sub.4)-haloalkoxycarbonyl, (C.sub.1-C.sub.4)-alkylcarboxy, (C.sub.3-C.sub.6)-cycloalkyl, (C.sub.3-C.sub.6)-cycloalkyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.4)-alkoxycarbonyl-(C.sub.1-C.sub.4)-alkyl, hydroxycarbonyl, hydroxycarbonyl-(C.sub.1-C.sub.4)-alkyl, R.sup.13R.sup.14N-carbonyl and has q oxo groups, R.sup.10, R.sup.11 are each independently (C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.6)-haloalkyl, (C.sub.2-C.sub.6)-alkenyl, (C.sub.2-C.sub.6)-haloalkenyl, (C.sub.2-C.sub.6)-alkynyl, (C.sub.2-C.sub.6)-haloalkynyl, (C.sub.1-C.sub.6)-alkoxy-(C.sub.1-C.sub.3)-alkyl, halogen-(C.sub.1-C.sub.6)-alkoxy-(C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.6)-alkoxy-(C.sub.2-C.sub.6)-alkoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylthio-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylsulphoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylsulphonyl-(C.sub.1-C.sub.3)-alkyl, (C.sub.3-C.sub.8)-cycloalkyl, (C.sub.3-C.sub.8)-cycloalkenyl, (C.sub.3-C.sub.8)-cycloalkyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.3-C.sub.8)-cycloalkenyl-(C.sub.1-C.sub.6)-alkyl, aryl, aryl-(C.sub.1-C.sub.3)-alkyl, heteroaryl, heteroaryl-(C.sub.1-C.sub.3)-alkyl, heterocyclyl or heterocyclyl-(C.sub.1-C.sub.3)-alkyl, wherein each of the last-mentioned 10 residues is unsubstituted or is substituted by one or more residues from the group consisting of halogen, nitro, hydroxyl, cyano, NR.sup.13R.sup.14, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, (C.sub.1-C.sub.4)-haloalkylthio, (C.sub.1-C.sub.4)-haloalkylsulphoxy, (C.sub.1-C.sub.4)-haloalkylsulphonyl, (C.sub.1-C.sub.4)-alkoxycarbonyl, (C.sub.1-C.sub.4)-haloalkoxycarbonyl, (C.sub.1-C.sub.4)-alkylcarboxy, (C.sub.3-C.sub.6)-cycloalkyl, (C.sub.3-C.sub.6)-cycloalkyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.4)-alkoxycarbonyl-(C.sub.1-C.sub.4)-alkyl, hydroxycarbonyl, hydroxycarbonyl-(C.sub.1-C.sub.4)-alkyl, R.sup.13R.sup.14N-carbonyl and wherein heterocyclyl has q oxo groups, or R.sup.10 and R.sup.11, together with the sulphur atom to which they are attached, form a 3- to 8-membered unsaturated, partially saturated or saturated ring, which comprises in each case, in addition to the carbon atoms and in addition to the sulphur atom, p ring members from the group consisting of N(R.sup.12).sub.m, O and S(O).sub.n and wherein said ring is unsubstituted or is substituted by one or more residues from the group consisting of halogen, nitro, hydroxyl, cyano, NR.sup.13R.sup.14, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, (C.sub.1-C.sub.4)-haloalkylthio, (C.sub.1-C.sub.4)-haloalkylsulphoxy, (C.sub.1-C.sub.4)-haloalkylsulphonyl, (C.sub.1-C.sub.4)-alkoxycarbonyl, (C.sub.1-C.sub.4)-haloalkoxycarbonyl, (C.sub.1-C.sub.4)-alkylcarboxy, (C.sub.3-C.sub.6)-cycloalkyl, (C.sub.3-C.sub.6)-cycloalkyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.4)-alkoxycarbonyl-(C.sub.1-C.sub.4)-alkyl, hydroxycarbonyl, hydroxycarbonyl-(C.sub.1-C.sub.4)-alkyl, R.sup.13R.sup.14N-carbonyl and has q oxo groups, R.sup.12 is hydrogen, (C.sub.1-C.sub.12)-alkyl, (C.sub.1-C.sub.12)-haloalkyl, (C.sub.2-C.sub.12)-alkenyl, (C.sub.2-C.sub.12)-haloalkenyl, (C.sub.2-C.sub.12)-alkynyl, (C.sub.2-C.sub.12)-haloalkynyl, (C.sub.3-C.sub.8)-cycloalkyl, (C.sub.3-C.sub.8)-halocycloalkyl, (C.sub.3-C.sub.8)-cycloalkenyl, (C.sub.3-C.sub.8)-cycloalkyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.3-C.sub.8)-cycloalkenyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.12)-alkylcarbonyl or (C.sub.1-C.sub.12)-haloalkylcarbonyl, R.sup.13, R.sup.14 are each independently hydrogen, (C.sub.1-C.sub.12)-alkyl, (C.sub.1-C.sub.12)-haloalkyl, (C.sub.2-C.sub.12)-alkenyl, (C.sub.2-C.sub.12)-haloalkenyl, (C.sub.2-C.sub.12)-alkynyl, (C.sub.2-C.sub.12)-haloalkynyl, (C.sub.1-C.sub.12)-alkylcarbonyl, (C.sub.2-C.sub.12)-alkenylcarbonyl, (C.sub.2-C.sub.12)-alkynylcarbonyl, (C.sub.1-C.sub.12)-haloalkylcarbonyl, (C.sub.1-C.sub.4)-alkylsulphonyl, (C.sub.3-C.sub.8)-cycloalkyl, (C.sub.3-C.sub.8)-cycloalkenyl, (C.sub.3-C.sub.8)-cycloalkyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.3-C.sub.8)-cycloalkenyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.3-C.sub.8)-cycloalkylcarbonyl, (C.sub.3-C.sub.8)-cycloalkenylcarbonyl, (C.sub.3-C.sub.8)-cycloalkyl-(C.sub.1-C.sub.6)-alkylcarbonyl, (C.sub.3-C.sub.8)-cycloalkenyl-(C.sub.1-C.sub.6)-alkylcarbonyl, aryl, arylcarbonyl, arylsulphonyl, hetaryl, hetarylcarbonyl, hetarylsulphonyl, heterocyclyl, heterocyclylcarbonyl, heterocyclylsulphonyl, wherein each of the last-mentioned 17 residues is unsubstituted or is substituted by one or more residues from the group consisting of halogen, nitro, hydroxyl, cyano, NH.sub.2, (C.sub.1-C.sub.6)-alkylamine, (C.sub.1-C.sub.6)-dialkylamine, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, (C.sub.1-C.sub.4)-haloalkylthio, (C.sub.1-C.sub.4)-haloalkylsulphoxy, (C.sub.1-C.sub.4)-haloalkylsulphonyl, (C.sub.1-C.sub.4)-alkoxycarbonyl, (C.sub.1-C.sub.4)-haloalkoxycarbonyl, (C.sub.1-C.sub.4)-alkylcarboxy, (C.sub.3-C.sub.6)-cycloalkyl, (C.sub.3-C.sub.6)-cycloalkyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.4)-alkoxycarbonyl-(C.sub.1-C.sub.4)-alkyl, hydroxycarbonyl, hydroxycarbonyl-(C.sub.1-C.sub.4)-alkyl and wherein heterocyclyl has q oxo groups, or R.sup.13 and R.sup.14, together with the nitrogen atom to which they are attached, form a 3- to 8-membered unsaturated, partially saturated or saturated ring, which comprises in each case, in addition to the carbon atoms and in addition to the nitrogen atom, p ring members from the group consisting of N(R.sup.12).sub.m, O and S(O).sub.n and wherein said ring is unsubstituted or is substituted by one or more residues from the group consisting of halogen, nitro, hydroxyl, cyano, NH.sub.2, (C.sub.1-C.sub.6)-alkylamine, (C.sub.1-C.sub.6)-dialkylamine, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, (C.sub.1-C.sub.4)-haloalkylthio, (C.sub.1-C.sub.4)-haloalkylsulphoxy, (C.sub.1-C.sub.4)-haloalkylsulphonyl, (C.sub.1-C.sub.4)-alkoxycarbonyl, (C.sub.1-C.sub.4)-haloalkoxycarbonyl, (C.sub.1-C.sub.4)-alkylcarboxy, (C.sub.3-C.sub.6)-cycloalkyl, (C.sub.3-C.sub.6)-cycloalkyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.4)-alkoxycarbonyl-(C.sub.1-C.sub.4)-alkyl, hydroxycarbonyl, hydroxycarbonyl-(C.sub.1-C.sub.4)-alkyl and has q oxo groups, n is independently selected from 0, 1 or 2, m is independently selected from 0 or 1, p is independently selected from 0, 1, 2 or 3, q is independently selected from 0, 1 or 2, y is 0 or 1, which is a herbicide and/or plant growth regulator.

    2. Compound of the formula (G) and/or a salt thereof, ##STR00024## in which A is CR.sup.6R.sup.7, W is O or S, R.sup.1 is hydrogen, (C.sub.1-C.sub.12)-alkyl, (C.sub.1-C.sub.12)-haloalkyl, (C.sub.2-C.sub.12)-alkenyl, (C.sub.2-C.sub.12)-haloalkenyl, (C.sub.2-C.sub.12)-alkynyl, (C.sub.2-C.sub.12)-haloalkynyl, NR.sup.13R.sup.14, R.sup.13R.sup.14N(C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.6)-alkoxy, (C.sub.1-C.sub.6)-haloalkoxy, (C.sub.1-C.sub.6)-haloalkoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.6)-alkoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.6)-alkoxy-(C.sub.2-C.sub.6)-alkoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, (C.sub.1-C.sub.4)-haloalkylthio, (C.sub.1-C.sub.4)-haloalkylsulphoxy, (C.sub.1-C.sub.4)-haloalkylsulphonyl, (C.sub.1-C.sub.4)-alkylthio-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylsulphoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylsulphonyl-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-haloalkylthio-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-haloalkylsulphoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-haloalkylsulphonyl-(C.sub.1-C.sub.3)-alkyl, (C.sub.3-C.sub.12)-cycloalkyl, (C.sub.3-C.sub.8)-cycloalkenyl, (C.sub.3-C.sub.12)-cycloalkyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.3-C.sub.8)-cycloalkenyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.3-C.sub.8)-cycloalkoxy, (C.sub.3-C.sub.8)-cycloalkyl-(C.sub.1-C.sub.6)-alkoxy, aryl, aryl-(C.sub.1-C.sub.3)-alkyl, heteroaryl, heteroaryl-(C.sub.1-C.sub.3)-alkyl, heterocyclyl, heterocyclyl-(C.sub.1-C.sub.3)-alkyl, aryloxy, heteroaryloxy, heterocyclyloxy, a bicyclic or a heterobicyclic residue, wherein each of the last-mentioned 17 residues is unsubstituted or is substituted by one or more residues from the group consisting of halogen, nitro, hydroxyl, cyano, NR.sup.13R.sup.14 (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, (C.sub.1-C.sub.4)-haloalkylthio, (C.sub.1-C.sub.4)-haloalkylsulphoxy, (C.sub.1-C.sub.4)-haloalkylsulphonyl, (C.sub.1-C.sub.4)-alkoxycarbonyl, (C.sub.1-C.sub.4)-haloalkoxycarbonyl, (C.sub.1-C.sub.4)-alkylcarboxy, (C.sub.3-C.sub.6)-cycloalkyl, (C.sub.3-C.sub.6)-cycloalkyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.4)-alkoxycarbonyl-(C.sub.1-C.sub.4)-alkyl, hydroxycarbonyl, hydroxycarbonyl-(C.sub.1-C.sub.4)-alkyl, R.sup.13R.sup.14N-carbonyl, and wherein heterocyclyl has q oxo groups, and wherein each of the aforementioned heterocyclic residues, in addition to the carbon atoms, has in each case p ring members from the group consisting of N(R.sup.12).sub.m, O and S(O).sub.n, R.sup.2 is hydrogen, (C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.6)-haloalkyl, (C.sub.2-C.sub.6)-alkenyl, (C.sub.2-C.sub.6)-haloalkenyl, (C.sub.2-C.sub.6)-alkynyl, (C.sub.2-C.sub.6)-haloalkynyl, (C.sub.1-C.sub.4)-alkylsulphonyl, (C.sub.1-C.sub.4)-haloalkylsulphonyl, (C.sub.1-C.sub.6)-alkylcarbonyl, (C.sub.2-C.sub.6)-alkenylcarbonyl, (C.sub.2-C.sub.6)-alkynylcarbonyl, (C.sub.1-C.sub.6)-haloalkylcarbonyl, (C.sub.2-C.sub.6)-haloalkenylcarbonyl, (C.sub.2-C.sub.6)-haloalkynylcarbonyl, (C.sub.1-C.sub.6)-alkoxycarbonyl, di((C.sub.1-C.sub.6)-alkyl)aminocarbonyl, (C.sub.3-C.sub.8)-cycloalkyl, (C.sub.3-C.sub.8)-cycloalkyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.3-C.sub.8)-cycloalkylcarbonyl, (C.sub.3-C.sub.8)-cycloalkyl-(C.sub.1-C.sub.6)-alkylcarbonyl, heteroarylcarbonyl, or arylcarbonyl, wherein each of the last-mentioned 6 residues is unsubstituted or is substituted by one or more residues from the group consisting of halogen, nitro, hydroxyl, cyano, NR.sup.13R.sup.14, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, (C.sub.1-C.sub.4)-haloalkylthio, (C.sub.1-C.sub.4)-haloalkylsulphoxy, (C.sub.1-C.sub.4)-haloalkylsulphonyl, (C.sub.1-C.sub.4)-alkoxycarbonyl, (C.sub.1-C.sub.4)-haloalkoxycarbonyl, (C.sub.1-C.sub.4)-alkylcarboxy, (C.sub.3-C.sub.6)-cycloalkyl, (C.sub.3-C.sub.6)-cycloalkyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.4)-alkoxycarbonyl-(C.sub.1-C.sub.4)-alkyl, hydroxycarbonyl, hydroxycarbonyl-(C.sub.1-C.sub.4)-alkyl, R.sup.13R.sup.14N-carbonyl, or R.sup.1 and R.sup.2, together with the nitrogen atom and (A).sub.y attached thereto form a 5- or 6-membered heterocyclic or heteroaromatic ring, which comprises in each case, in addition to the carbon atoms and the nitrogen atom, p ring members from the group consisting of N(R.sup.12).sub.m, O and S(O).sub.n and wherein said ring is unsubstituted or is substituted by one or more residues from the group consisting of halogen, nitro, hydroxyl, cyano, NR.sup.13R.sup.14, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, (C.sub.1-C.sub.4)-haloalkylthio, (C.sub.1-C.sub.4)-haloalkylsulphoxy, (C.sub.1-C.sub.4)-haloalkylsulphonyl, (C.sub.1-C.sub.4)-alkoxycarbonyl, (C.sub.1-C.sub.4)-haloalkoxycarbonyl, (C.sub.1-C.sub.4)-alkylcarboxy, (C.sub.3-C.sub.6)-cycloalkyl, (C.sub.3-C.sub.6)-cycloalkyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.4)-alkoxycarbonyl-(C.sub.1-C.sub.4)-alkyl, hydroxycarbonyl, hydroxycarbonyl-(C.sub.1-C.sub.4)-alkyl, R.sup.13R.sup.14N-carbonyl and has q oxo groups, R.sup.3 is hydrogen, halogen, azido, isocyanate, isothiocyanate, nitro, cyano, hydroxyl, NR.sup.13R.sup.14, tri(C.sub.1-C.sub.6)-alkylsilyl, (C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.6)-haloalkyl, (C.sub.2-C.sub.6)-alkenyl, (C.sub.2-C.sub.6)-haloalkenyl, (C.sub.2-C.sub.6)-alkynyl, (C.sub.2-C.sub.6)-haloalkynyl, (C.sub.1-C.sub.6)-alkoxy, (C.sub.1-C.sub.6)-haloalkoxy, (C.sub.1-C.sub.6)-haloalkoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.6)-alkoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.6)-alkoxy-(C.sub.2-C.sub.6)-alkoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.6)-alkylcarbonyloxy, (C.sub.1-C.sub.6)-haloalkylcarbonyloxy, (C.sub.2-C.sub.6)-alkenylcarbonyloxy, (C.sub.2-C.sub.6)-alkynylcarbonyloxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, (C.sub.1-C.sub.4)-haloalkylthio, (C.sub.1-C.sub.4)-haloalkylsulphoxy, (C.sub.1-C.sub.4)-haloalkylsulphonyl, (C.sub.1-C.sub.4)-alkylthio-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylsulphoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylsulphonyl-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-haloalkylthio-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-haloalkylsulphoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-haloalkylsulphonyl-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.6)-alkoxycarbonyl, (C.sub.1-C.sub.6)-haloalkoxycarbonyl, (C.sub.2-C.sub.6)-alkenyloxycarbonyl, (C.sub.2-C.sub.6)-haloalkenyloxycarbonyl, (C.sub.2-C.sub.6)-alkynyloxycarbonyl, (C.sub.2-C.sub.6)-haloalkynyloxycarbonyl, (C.sub.1-C.sub.6)-alkylcarbonyl, (C.sub.1-C.sub.6)-haloalkylcarbonyl, (C.sub.2-C.sub.6)-alkenylcarbonyl, (C.sub.2-C.sub.6)-haloalkenylcarbonyl, (C.sub.2-C.sub.6)-alkynylcarbonyl, (C.sub.2-C.sub.6)-haloalkynylcarbonyl, R.sup.13R.sup.14N-carbonyl, arylthio, arylsulphoxy, arylsulphonyl, (C.sub.3-C.sub.8)-cycloalkyl, (C.sub.3-C.sub.8)-cycloalkenyl, (C.sub.3-C.sub.8)-cycloalkyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.3-C.sub.8)-cycloalkenyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.3-C.sub.8)-cycloalkoxy, aryl, aryloxy, arylcarbonyloxy, aryl-(C.sub.1-C.sub.3)-alkyl, heteroaryl, heteroaryloxy, heteroaryl-(C.sub.1-C.sub.3)-alkyl, heterocyclyl, heterocyclyloxy, or heterocyclyl-(C.sub.1-C.sub.3)-alkyl, wherein each of the last-mentioned 18 residues is unsubstituted or is substituted by one or more residues from the group consisting of halogen, nitro, hydroxyl, cyano, NR.sup.13R.sup.14, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, (C.sub.1-C.sub.4)-haloalkylthio, (C.sub.1-C.sub.4)-haloalkylsulphoxy, (C.sub.1-C.sub.4)-haloalkylsulphonyl, (C.sub.1-C.sub.4)-alkoxycarbonyl, (C.sub.1-C.sub.4)-haloalkoxycarbonyl, (C.sub.1-C.sub.4)-alkylcarboxy, (C.sub.3-C.sub.6)-cycloalkyl, (C.sub.3-C.sub.6)-cycloalkyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.4)-alkoxycarbonyl-(C.sub.1-C.sub.4)-alkyl, hydroxycarbonyl, hydroxycarbonyl-(C.sub.1-C.sub.4)-alkyl, R.sup.13R.sup.14N-carbonyl, and wherein heterocyclyl has q oxo groups, R.sup.4, R.sup.5 are each independently hydrogen, (C.sub.1-C.sub.12)-alkyl, (C.sub.1-C.sub.12)-haloalkyl, (C.sub.2-C.sub.12)-alkenyl, (C.sub.2-C.sub.12)-haloalkenyl, (C.sub.2-C.sub.12)-alkynyl, (C.sub.2-C.sub.12)-haloalkynyl, (C.sub.1-C.sub.6)-alkoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.6)-alkoxy-(C.sub.2-C.sub.6)-alkoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.6)-alkoxy-(C.sub.1-C.sub.3)-alkylcarbonyl, (C.sub.1-C.sub.6)-alkoxy-(C.sub.2-C.sub.6)-alkoxy-(C.sub.1-C.sub.3)-alkylcarbonyl, (C.sub.1-C.sub.6)-alkoxycarbonyl, (C.sub.1-C.sub.6)-haloalkoxycarbonyl, (C.sub.2-C.sub.6)-alkenyloxycarbonyl, (C.sub.2-C.sub.6)-haloalkenyloxycarbonyl, (C.sub.2-C.sub.6)-alkynyloxycarbonyl, (C.sub.2-C.sub.6)-haloalkynyloxycarbonyl, (C.sub.1-C.sub.6)-alkylcarbonyl, (C.sub.1-C.sub.6)-haloalkylcarbonyl, (C.sub.2-C.sub.6)-alkenylcarbonyl, (C.sub.2-C.sub.6)-haloalkenylcarbonyl, (C.sub.2-C.sub.6)-alkynylcarbonyl, (C.sub.2-C.sub.6)-haloalkynylcarbonyl, R.sup.13R.sup.14N-carbonyl, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-haloalkylthio, (C.sub.1-C.sub.8)-alkylthiocarbonyl, (C.sub.1-C.sub.8)-haloalkylthiocarbonyl, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-haloalkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, (C.sub.1-C.sub.4)-haloalkylsulphonyl, (C.sub.1-C.sub.4)-alkylthio-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylsulphoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylsulphonyl-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylthio-(C.sub.1-C.sub.3)-alkylcarbonyl, (C.sub.1-C.sub.4)-alkylsulphoxy-(C.sub.1-C.sub.3)-alkylcarbonyl, (C.sub.1-C.sub.4)-alkylsulphonyl-(C.sub.1-C.sub.3)-alkylcarbonyl, (C.sub.1-C.sub.12)-alkylcarbonyl, (C.sub.1-C.sub.12)-haloalkylcarbonyl, (C.sub.2-C.sub.12)-alkenylcarbonyl, (C.sub.2-C.sub.12)-haloalkenylcarbonyl, (C.sub.2-C.sub.12)-alkynylcarbonyl, (C.sub.2-C.sub.12)-haloalkynylcarbonyl, (C.sub.1-C.sub.12)-alkoxycarbonylcarbonyl, (C.sub.1-C.sub.12)-alkoxycarbonyl-(C.sub.1-C.sub.3)-alkylcarbonyl, (C.sub.3-C.sub.8)-cycloalkyl, (C.sub.3-C.sub.8)-cycloalkenyl, (C.sub.3-C.sub.8)-cycloalkyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.3-C.sub.8)-cycloalkenyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.3-C.sub.8)-cycloalkylcarbonyl, (C.sub.3-C.sub.8)-cycloalkenylcarbonyl, (C.sub.3-C.sub.8)-cycloalkyl-(C.sub.1-C.sub.6)-alkylcarbonyl, (C.sub.3-C.sub.8)-cycloalkenyl-(C.sub.1-C.sub.6)-alkylcarbonyl, aryl, aryl-(C.sub.1-C.sub.3)-alkyl, heteroaryl, heteroaryl-(C.sub.1-C.sub.3)-alkyl, heterocyclyl, heterocyclyl-(C.sub.1-C.sub.3)-alkyl, arylcarbonyl, aryl-(C.sub.1-C.sub.6)-alkylcarbonyl, heteroarylcarbonyl, heteroaryl-(C.sub.1-C.sub.6)-alkylcarbonyl, heterocyclylcarbonyl, or heterocyclyl-(C.sub.1-C.sub.6)-alkylcarbonyl, wherein each of the last-mentioned 20 residues is unsubstituted or is substituted by one or more residues from the group consisting of halogen, nitro, hydroxyl, cyano, NR.sup.13R.sup.14, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, (C.sub.1-C.sub.4)-haloalkylthio, (C.sub.1-C.sub.4)-haloalkylsulphoxy, (C.sub.1-C.sub.4)-haloalkylsulphonyl, (C.sub.1-C.sub.4)-alkoxycarbonyl, (C.sub.1-C.sub.4)-haloalkoxycarbonyl, (C.sub.1-C.sub.4)-alkylcarboxy, (C.sub.3-C.sub.6)-cycloalkyl, (C.sub.3-C.sub.6)-cycloalkyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.4)-alkoxycarbonyl-(C.sub.1-C.sub.4)-alkyl, hydroxycarbonyl, hydroxycarbonyl-(C.sub.1-C.sub.4)-alkyl, R.sup.13R.sup.14N-carbonyl, and wherein heterocyclyl has q oxo groups, wherein R.sup.4 and R.sup.5 are not both an alkyl residue, or NR.sup.4R.sup.5 is NCR.sup.8R.sup.9 or NS(O).sub.nR.sup.10R.sup.11, R.sup.6, R.sup.7 are each independently hydrogen, cyano, halogen, (C.sub.1-C.sub.6)-alkyl, (C.sub.2-C.sub.6)-alkenyl, (C.sub.2-C.sub.6)-alkynyl, or (C.sub.3-C.sub.8)-cycloalkyl, or R.sup.6 and R.sup.7, together with the carbon atom to which they are attached, form a 3-6-membered carbocyclic or heterocyclic ring, which comprises in each case, in addition to the carbon atoms, p ring members from the group consisting of N(R.sup.12).sub.m, O and S(O).sub.n and wherein said ring is unsubstituted or is substituted by one or more residues from the group consisting of halogen, nitro, hydroxyl, cyano, NR.sup.13R.sup.14, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, (C.sub.1-C.sub.4)-haloalkylthio, (C.sub.1-C.sub.4)-haloalkylsulphoxy, (C.sub.1-C.sub.4)-haloalkylsulphonyl, (C.sub.1-C.sub.4)-alkoxycarbonyl, (C.sub.1-C.sub.4)-haloalkoxycarbonyl, (C.sub.1-C.sub.4)-alkylcarboxy, (C.sub.3-C.sub.6)-cycloalkyl, (C.sub.3-C.sub.6)-cycloalkyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.4)-alkoxycarbonyl-(C.sub.1-C.sub.4)-alkyl, hydroxycarbonyl, hydroxycarbonyl-(C.sub.1-C.sub.4)-alkyl, R.sup.13R.sup.14N-carbonyl and has q oxo groups, R.sup.8, R.sup.9 are each independently hydrogen, (C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.6)-haloalkyl, (C.sub.2-C.sub.6)-alkenyl, (C.sub.2-C.sub.6)-haloalkenyl, (C.sub.2-C.sub.6)-alkynyl, (C.sub.2-C.sub.6)-haloalkynyl, (C.sub.1-C.sub.6)-alkoxy, (C.sub.1-C.sub.6)-haloalkoxy, (C.sub.1-C.sub.6)-haloalkoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.2-C.sub.6)-alkenyloxy, (C.sub.2-C.sub.6)-haloalkenyloxy, (C.sub.2-C.sub.6)-alkynyloxy, (C.sub.2-C.sub.6)-haloalkynyloxy, NR.sup.13R.sup.14, (C.sub.1-C.sub.6)-alkoxy-(C.sub.1-C.sub.3)-alkyl, halogen-(C.sub.1-C.sub.6)-alkoxy-(C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.6)-alkoxy-(C.sub.2-C.sub.6)-alkoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylthio-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylsulphoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylsulphonyl-(C.sub.1-C.sub.3)-alkyl, (C.sub.3-C.sub.8)-cycloalkyl, (C.sub.3-C.sub.8)-cycloalkenyl, (C.sub.3-C.sub.8)-cycloalkyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.3-C.sub.8)-cycloalkenyl-(C.sub.1-C.sub.6)-alkyl, aryl, aryl-(C.sub.1-C.sub.3)-alkyl, heteroaryl, heteroaryl-(C.sub.1-C.sub.3)-alkyl, heterocyclyl, heterocyclyl-(C.sub.1-C.sub.3)-alkyl, wherein each of the last-mentioned 10 residues is unsubstituted or is substituted by one or more residues from the group consisting of halogen, nitro, hydroxyl, cyano, NR.sup.13R.sup.14, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, (C.sub.1-C.sub.4)-haloalkylthio, (C.sub.1-C.sub.4)-haloalkylsulphoxy, (C.sub.1-C.sub.4)-haloalkylsulphonyl, (C.sub.1-C.sub.4)-alkoxycarbonyl, (C.sub.1-C.sub.4)-haloalkoxycarbonyl, (C.sub.1-C.sub.4)-alkylcarboxy, (C.sub.3-C.sub.6)-cycloalkyl, (C.sub.3-C.sub.6)-cycloalkyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.4)-alkoxycarbonyl-(C.sub.1-C.sub.4)-alkyl, hydroxycarbonyl, hydroxycarbonyl-(C.sub.1-C.sub.4)-alkyl, R.sup.13R.sup.14N-carbonyl and has q oxo groups, or R.sup.8 and R.sup.9, together with the carbon atom to which they are attached, form a 3- to 8-membered unsaturated, partially saturated or saturated ring, which comprises in each case, in addition to the carbon atoms, p ring members from the group consisting of N(R.sup.12).sub.m, O and S(O).sub.n and wherein said ring is unsubstituted or is substituted by one or more residues from the group consisting of halogen, nitro, hydroxyl, cyano, NR.sup.13R.sup.14, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, (C.sub.1-C.sub.4)-haloalkylthio, (C.sub.1-C.sub.4)-haloalkylsulphoxy, (C.sub.1-C.sub.4)-haloalkylsulphonyl, (C.sub.1-C.sub.4)-alkoxycarbonyl, (C.sub.1-C.sub.4)-haloalkoxycarbonyl, (C.sub.1-C.sub.4)-alkylcarboxy, (C.sub.3-C.sub.6)-cycloalkyl, (C.sub.3-C.sub.6)-cycloalkyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.4)-alkoxycarbonyl-(C.sub.1-C.sub.4)-alkyl, hydroxycarbonyl, hydroxycarbonyl-(C.sub.1-C.sub.4)-alkyl, R.sup.13R.sup.14N-carbonyl and has q oxo groups, R.sup.10, R.sup.11 are each independently (C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.6)-haloalkyl, (C.sub.2-C.sub.6)-alkenyl, (C.sub.2-C.sub.6)-haloalkenyl, (C.sub.2-C.sub.6)-alkynyl, (C.sub.2-C.sub.6)-haloalkynyl, (C.sub.1-C.sub.6)-alkoxy-(C.sub.1-C.sub.3)-alkyl, halogen-(C.sub.1-C.sub.6)-alkoxy-(C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.6)-alkoxy-(C.sub.2-C.sub.6)-alkoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylthio-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylsulphoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylsulphonyl-(C.sub.1-C.sub.3)-alkyl, (C.sub.3-C.sub.8)-cycloalkyl, (C.sub.3-C.sub.8)-cycloalkenyl, (C.sub.3-C.sub.8)-cycloalkyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.3-C.sub.8)-cycloalkenyl-(C.sub.1-C.sub.6)-alkyl, aryl, aryl-(C.sub.1-C.sub.3)-alkyl, heteroaryl, heteroaryl-(C.sub.1-C.sub.3)-alkyl, heterocyclyl or heterocyclyl-(C.sub.1-C.sub.3)-alkyl, wherein each of the last-mentioned 10 residues is unsubstituted or is substituted by one or more residues from the group consisting of halogen, nitro, hydroxyl, cyano, NR.sup.13R.sup.14, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, (C.sub.1-C.sub.4)-haloalkylthio, (C.sub.1-C.sub.4)-haloalkylsulphoxy, (C.sub.1-C.sub.4)-haloalkylsulphonyl, (C.sub.1-C.sub.4)-alkoxycarbonyl, (C.sub.1-C.sub.4)-haloalkoxycarbonyl, (C.sub.1-C.sub.4)-alkylcarboxy, (C.sub.3-C.sub.6)-cycloalkyl, (C.sub.3-C.sub.6)-cycloalkyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.4)-alkoxycarbonyl-(C.sub.1-C.sub.4)-alkyl, hydroxycarbonyl, hydroxycarbonyl-(C.sub.1-C.sub.4)-alkyl, R.sup.13R.sup.14N-carbonyl and wherein heterocyclyl has q oxo groups, or R.sup.10 and R.sup.11, together with the sulphur atom to which they are attached, form a 3- to 8-membered unsaturated, partially saturated or saturated ring, which comprises in each case, in addition to the carbon atoms and in addition to the sulphur atom, p ring members from the group consisting of N(R.sup.12).sub.m, O and S(O).sub.n and wherein said ring is unsubstituted or is substituted by one or more residues from the group consisting of halogen, nitro, hydroxyl, cyano, NR.sup.13R.sup.14, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, (C.sub.1-C.sub.4)-haloalkylthio, (C.sub.1-C.sub.4)-haloalkylsulphoxy, (C.sub.1-C.sub.4)-haloalkylsulphonyl, (C.sub.1-C.sub.4)-alkoxycarbonyl, (C.sub.1-C.sub.4)-haloalkoxycarbonyl, (C.sub.1-C.sub.4)-alkylcarboxy, (C.sub.3-C.sub.6)-cycloalkyl, (C.sub.3-C.sub.6)-cycloalkyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.4)-alkoxycarbonyl-(C.sub.1-C.sub.4)-alkyl, hydroxycarbonyl, hydroxycarbonyl-(C.sub.1-C.sub.4)-alkyl, R.sup.13R.sup.14N-carbonyl and has q oxo groups, R.sup.12 is hydrogen, (C.sub.12)-haloalkyl, (C.sub.2-C.sub.12)-alkenyl, (C.sub.2-C.sub.12)-haloalkenyl, (C.sub.2-C.sub.12)-alkynyl, (C.sub.2-C.sub.12)-haloalkynyl, (C.sub.3-C.sub.8)-cycloalkyl, (C.sub.3-C.sub.8)-halocycloalkyl, (C.sub.3-C.sub.8)-cycloalkenyl, (C.sub.3-C.sub.8)-cycloalkyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.3-C.sub.8)-cycloalkenyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.12)-alkylcarbonyl or (C.sub.12)-haloalkylcarbonyl, R.sup.13, R.sup.11 are each independently hydrogen, (C.sub.1-C.sub.12)-alkyl, (C.sub.2-C.sub.12)-alkenyl, (C.sub.2-C.sub.12)-haloalkenyl, (C.sub.2-C.sub.12)-alkynyl, (C.sub.2-C.sub.12)-haloalkynyl, (C.sub.1-C.sub.12)-alkylcarbonyl, (C.sub.2-C.sub.12)-alkenylcarbonyl, (C.sub.2-C.sub.12)-alkynylcarbonyl, (C.sub.1-C.sub.12)-haloalkylcarbonyl, (C.sub.1-C.sub.4)-alkylsulphonyl, (C.sub.3-C.sub.8)-cycloalkyl, (C.sub.3-C.sub.8)-cycloalkenyl, (C.sub.3-C.sub.8)-cycloalkyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.3-C.sub.8)-cycloalkenyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.3-C.sub.8)-cycloalkylcarbonyl, (C.sub.3-C.sub.8)-cycloalkenylcarbonyl, (C.sub.3-C.sub.8)-cycloalkyl-(C.sub.1-C.sub.6)-alkylcarbonyl, (C.sub.3-C.sub.8)-cycloalkenyl-(C.sub.1-C.sub.6)-alkylcarbonyl, aryl, arylcarbonyl, arylsulphonyl, hetaryl, hetarylcarbonyl, hetarylsulphonyl, heterocyclyl, heterocyclylcarbonyl, heterocyclylsulphonyl, wherein each of the last-mentioned 17 residues is unsubstituted or is substituted by one or more residues from the group consisting of halogen, nitro, hydroxyl, cyano, NH.sub.2, (C.sub.1-C.sub.6)-alkylamine, (C.sub.1-C.sub.6)-dialkylamine, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, (C.sub.1-C.sub.4)-haloalkylthio, (C.sub.1-C.sub.4)-haloalkylsulphoxy, (C.sub.1-C.sub.4)-haloalkylsulphonyl, (C.sub.1-C.sub.4)-alkoxycarbonyl, (C.sub.1-C.sub.4)-haloalkoxycarbonyl, (C.sub.1-C.sub.4)-alkylcarboxy, (C.sub.3-C.sub.6)-cycloalkyl, (C.sub.3-C.sub.6)-cycloalkyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.4)-alkoxycarbonyl-(C.sub.1-C.sub.4)-alkyl, hydroxycarbonyl, hydroxycarbonyl-(C.sub.1-C.sub.4)-alkyl and wherein heterocyclyl has q oxo groups, or R.sup.3 and R.sup.14, together with the nitrogen atom to which they are attached, form a 3- to 8-membered unsaturated, partially saturated or saturated ring, which comprises in each case, in addition to the carbon atoms and in addition to the nitrogen atom, p ring members from the group consisting of N(R.sup.12).sub.m, O and S(O).sub.n and wherein said ring is unsubstituted or is substituted by one or more residues from the group consisting of halogen, nitro, hydroxyl, cyano, NH.sub.2, (C.sub.1-C.sub.6)-alkylamine, (C.sub.1-C.sub.6)-dialkylamine, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, (C.sub.1-C.sub.4)-haloalkylthio, (C.sub.1-C.sub.4)-haloalkylsulphoxy, (C.sub.1-C.sub.4)-haloalkylsulphonyl, (C.sub.1-C.sub.4)-alkoxycarbonyl, (C.sub.1-C.sub.4)-haloalkoxycarbonyl, (C.sub.1-C.sub.4)-alkylcarboxy, (C.sub.3-C.sub.6)-cycloalkyl, (C.sub.3-C.sub.6)-cycloalkyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.4)-alkoxycarbonyl-(C.sub.1-C.sub.4)-alkyl, hydroxycarbonyl, hydroxycarbonyl-(C.sub.1-C.sub.4)-alkyl and has q oxo groups, n is independently selected from 0, 1 or 2, m is independently selected from 0 or 1, p is independently selected from 0, 1, 2 or 3, q is independently selected from 0, 1 or 2, y is 0 or 1, with the proviso that: the compound of formula (G) is not 3-amino-5-(morpholin-4-ylcarbonothioyl)-1,2-thiazole-4-carbonitrile, and y is 1, if R.sup.1 is a substituted 4-heptafluoroisopropylphenyl residue, a substituted 4-(nonafluoro-2-butyl)phenyl residue, a substituted 4-(1,1,2,3,3,3-hexafluoropropoxy)phenyl residue, a 2-bromo-4-methyl-6-(heptafluoroisopropyl)pyridin-3-yl residue or a 2-bromo-4-methyl-6-(2,2,2-trifluoro-1-trifluoromethylethoxy)pyridin-3-yl residue.

    3. Compound of the formula (G) according to claim 2 and/or a salt thereof, in which A is CR.sup.6R.sup.7, W is O or S, R.sup.1 is hydrogen, (C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.6)-haloalkyl, (C.sub.2-C.sub.6)-alkenyl, (C.sub.2-C.sub.6)-alkynyl, NR.sup.13R.sup.14, R.sup.13R.sup.14N(C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.6)-alkoxy, (C.sub.1-C.sub.6)-haloalkoxy, (C.sub.1-C.sub.6)-haloalkoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.6)-alkoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.6)-alkoxy-(C.sub.2-C.sub.6)-alkoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, (C.sub.1-C.sub.4)-alkylthio-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylsulphoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylsulphonyl-(C.sub.1-C.sub.3)-alkyl, (C.sub.3-C.sub.6)-cycloalkyl, (C.sub.3-C.sub.6)-cycloalkenyl, (C.sub.3-C.sub.6)-cycloalkyl-(C.sub.1-C.sub.3)-alkyl, (C.sub.3-C.sub.6)-cycloalkenyl-(C.sub.1-C.sub.3)-alkyl, (C.sub.3-C.sub.6)-cycloalkoxy, phenyl, heteroaryl, heterocyclyl, phenoxy, heteroaryloxy, heterocyclyloxy or a carbobicyclic residue, wherein each of the last-mentioned 12 residues is unsubstituted or is substituted by one or more residues from the group consisting of halogen, nitro, hydroxyl, cyano, NR.sup.13R.sup.14, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, and wherein heterocyclyl has q oxo groups, R.sup.2 is hydrogen, (C.sub.1-C.sub.6)-alkyl, (C.sub.2-C.sub.6)-alkenyl, (C.sub.2-C.sub.6)-alkynyl, (C.sub.1-C.sub.4)-alkylsulphonyl, (C.sub.1-C.sub.4)-haloalkylsulphonyl, (C.sub.1-C.sub.6)-alkylcarbonyl, (C.sub.2-C.sub.6)-alkenylcarbonyl, (C.sub.2-C.sub.6)-alkynylcarbonyl, (C.sub.1-C.sub.6)-alkoxycarbonyl, di((C.sub.1-C.sub.6)-alkyl)aminocarbonyl, (C.sub.3-C.sub.8)-cycloalkylcarbonyl, heteroarylcarbonyl or phenylcarbonyl, wherein each of the last-mentioned 3 residues is unsubstituted or is substituted by one or more residues from the group consisting of halogen, nitro, cyano, NR.sup.13R.sup.14, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, R.sup.3 is halogen, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.2-C.sub.4)-alkenyl, (C.sub.2-C.sub.4)-haloalkenyl, (C.sub.2-C.sub.4)-alkynyl, (C.sub.1-C.sub.6)-alkoxy, (C.sub.1-C.sub.6)-haloalkoxy, (C.sub.1-C.sub.6)-haloalkoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, (C.sub.1-C.sub.4)-haloalkylthio, (C.sub.1-C.sub.4)-haloalkylsulphoxy, (C.sub.1-C.sub.4)-haloalkylsulphonyl, (C.sub.3-C.sub.8)-cycloalkyl, phenyl, phenyloxy, phenylthio, phenylsulphoxy, phenylsulphonyl, wherein each of the last-mentioned 6 residues is unsubstituted or is substituted by one or more residues from the group consisting of halogen, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, R.sup.4, R.sup.5 are each independently hydrogen, (C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.6)-haloalkyl, (C.sub.2-C.sub.6)-alkenyl, (C.sub.2-C.sub.6)-alkynyl, (C.sub.1-C.sub.6)-alkoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.6)-alkoxy-(C.sub.1-C.sub.3)-alkylcarbonyl, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-haloalkylthio, (C.sub.1-C.sub.4)-alkylthiocarbonyl, (C.sub.1-C.sub.4)-haloalkylthiocarbonyl, (C.sub.1-C.sub.4)-alkylthio-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylsulphoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylsulphonyl-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylthio-(C.sub.1-C.sub.3)-alkylcarbonyl, (C.sub.1-C.sub.4)-alkylsulphoxy-(C.sub.1-C.sub.3)-alkylcarbonyl, (C.sub.1-C.sub.4)-alkylsulphonyl-(C.sub.1-C.sub.3)-alkylcarbonyl, (C.sub.1-C.sub.6)-alkylcarbonyl, (C.sub.1-C.sub.6)-haloalkylcarbonyl, (C.sub.2-C.sub.6)-alkenylcarbonyl, (C.sub.2-C.sub.6)-alkynylcarbonyl, (C.sub.1-C.sub.6)-alkoxycarbonylcarbonyl, (C.sub.1-C.sub.6)-alkoxycarbonyl-(C.sub.1-C.sub.3)-alkylcarbonyl, (C.sub.1-C.sub.6)-alkoxycarbonyl, (C.sub.1-C.sub.6)-haloalkoxycarbonyl, (C.sub.2-C.sub.6)-alkenyloxycarbonyl, (C.sub.3-C.sub.6)-cycloalkyl, (C.sub.3-C.sub.6)-cycloalkyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.3-C.sub.6)-cycloalkylcarbonyl, (C.sub.3-C.sub.6)-cycloalkyl-(C.sub.1-C.sub.6)-alkylcarbonyl, phenyl, phenyl-(C.sub.1-C.sub.3)-alkyl, heteroaryl, heteroaryl-(C.sub.1-C.sub.3)-alkyl, heterocyclyl, heterocyclyl-(C.sub.1-C.sub.3)-alkyl, phenylcarbonyl, phenyl-(C.sub.1-C.sub.6)-alkylcarbonyl, hetarylcarbonyl, hetaryl-(C.sub.1-C.sub.6)-alkylcarbonyl, heterocyclylcarbonyl, heterocyclyl-(C.sub.1-C.sub.6)-alkylcarbonyl, wherein each of the last-mentioned 16 residues is unsubstituted or is substituted by one or more residues from the group consisting of halogen, nitro, hydroxyl, cyano, NR.sup.13R.sup.14, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, and wherein heterocyclyl has q oxo groups, wherein R.sup.4 and R.sup.5 are not both an alkyl residue, or NR.sup.4R.sup.5 is NCR.sup.8R.sup.9 or NS(O).sub.nR.sup.10R.sup.11, R.sup.6, R.sup.7 are each independently hydrogen or (C.sub.1-C.sub.6)-alkyl, R.sup.8, R.sup.9 are each independently hydrogen, (C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.6)-haloalkyl, (C.sub.2-C.sub.6)-alkenyl, (C.sub.2-C.sub.6)-alkynyl, (C.sub.1-C.sub.6)-alkoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylthio-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylsulphoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylsulphonyl-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.6)-alkoxy, (C.sub.1-C.sub.6)-haloalkoxy, (C.sub.2-C.sub.6)-alkenyloxy, NR.sup.13R.sup.14, (C.sub.3-C.sub.8)-cycloalkyl, (C.sub.3-C.sub.8)-cycloalkyl-(C.sub.1-C.sub.6)-alkyl, phenyl, phenyl-(C.sub.1-C.sub.3)-alkyl, heteroaryl, heteroaryl-(C.sub.1-C.sub.3)-alkyl, heterocyclyl, heterocyclyl-(C.sub.1-C.sub.3)-alkyl, wherein each of the last-mentioned 8 residues is unsubstituted or is substituted by one or more residues from the group consisting of halogen, nitro, hydroxyl, cyano, NR.sup.13R.sup.14, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, and wherein heterocyclyl has q oxo groups, or R.sup.8 and R.sup.9, together with the carbon atom to which they are attached, form a 3- to 6-membered unsaturated, partially saturated or saturated ring, which comprises in each case, in addition to the carbon atoms, p ring members from the group consisting of N(R.sup.12).sub.m, O and S(O).sub.n, and wherein said ring is unsubstituted or is substituted by one or more residues from the group consisting of halogen, nitro, hydroxyl, cyano, NR.sup.13R.sup.14, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, and wherein heterocyclyl has q oxo groups, R.sup.10, R.sup.11 are each independently, (C.sub.1-C.sub.6)-alkyl, (C.sub.2-C.sub.6)-alkenyl, (C.sub.2-C.sub.6)-alkynyl, (C.sub.1-C.sub.6)-alkoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylthio-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylsulphoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylsulphonyl-(C.sub.1-C.sub.3)-alkyl, (C.sub.3-C.sub.8)-cycloalkyl, (C.sub.3-C.sub.8)-cycloalkyl-(C.sub.1-C.sub.6)-alkyl, phenyl, phenyl-(C.sub.1-C.sub.3)-alkyl, heteroaryl, heteroaryl-(C.sub.1-C.sub.3)-alkyl, heterocyclyl, heterocyclyl-(C.sub.1-C.sub.3)-alkyl, wherein each of the last-mentioned 8 residues is unsubstituted or is substituted by one or more residues from the group consisting of halogen, nitro, hydroxyl, cyano, NR.sup.13R.sup.14, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, and wherein heterocyclyl has q oxo groups, or R.sup.10 and R.sup.11, together with the sulphur atom to which they are attached, form a 3- to 6-membered unsaturated, partially saturated or saturated ring, which comprises in each case, in addition to the carbon atoms and in addition to the sulphur atom, p ring members from the group consisting of N(R.sup.12).sub.m, O and S(O).sub.n, and wherein said ring is unsubstituted or is substituted by one or more residues from the group consisting of halogen, nitro, hydroxyl, cyano, NR.sup.13R.sup.14, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy or (C.sub.1-C.sub.4)-alkylsulphonyl, and wherein heterocyclyl has q oxo groups, R.sup.12 is hydrogen, (C.sub.1-C.sub.6)-alkyl or (C.sub.1-C.sub.6)-alkylcarbonyl, R.sup.13, R.sup.14 are each independently hydrogen, (C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.6)-alkylcarbonyl, (C.sub.1-C.sub.4)-alkylsulphonyl, phenyl, phenylcarbonyl, wherein each of the last-mentioned two residues is unsubstituted or is substituted by one or more residues from the group consisting of halogen, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, or R.sup.13 and R.sup.14, together with the nitrogen atom to which they are attached, form a 3- to 8-membered unsaturated, partially saturated or saturated ring, which comprises in each case, in addition to the carbon atoms and in addition to the nitrogen atom, p ring members from the group consisting of N(R.sup.12).sub.m, O and S(O).sub.n, and wherein said ring is unsubstituted or is substituted by one or more residues from the group consisting of halogen, hydroxyl, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, and has q oxo groups, n is independently selected from 0, 1 or 2, m is independently selected from 0 or 1, p is independently selected from 0, 1 or 2, q is independently selected from 0, 1 or 2, y is 0 or 1, with the proviso that: y is 1, if R.sup.1 is a substituted 4-heptafluoroisopropylphenyl residue, a substituted 4-(nonafluoro-2-butyl)phenyl residue, a substituted 4-(1,1,2,3,3,3-hexafluoropropoxy)phenyl residue, a 2-bromo-4-methyl-6-(heptafluoroisopropyl)pyridin-3-yl residue or a 2-bromo-4-methyl-6-(2,2,2-trifluoro-1-trifluoromethylethoxy)pyridin-3-yl residue.

    4. Compound of the formula (G) according to claim 2, and/or a salt thereof, in which A is CR.sup.6R.sup.7, W is O or S, R.sup.1 is (C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.6)-haloalkyl, (C.sub.2-C.sub.6)-alkenyl, (C.sub.2-C.sub.6)-alkynyl, NR.sup.13R.sup.14, R.sup.13R.sup.14N(C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.6)-alkoxy, (C.sub.1-C.sub.6)-haloalkoxy, (C.sub.1-C.sub.6)-alkoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.6)-alkoxy-(C.sub.2-C.sub.6)-alkoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, (C.sub.1-C.sub.4)-alkylthio-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylsulphoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylsulphonyl-(C.sub.1-C.sub.3)-alkyl, (C.sub.3-C.sub.6)-cycloalkyl, (C.sub.3-C.sub.6)-cycloalkenyl, (C.sub.3-C.sub.6)-cycloalkyl-(C.sub.1-C.sub.3)-alkyl, (C.sub.3-C.sub.6)-cycloalkenyl-(C.sub.1-C.sub.3)-alkyl, (C.sub.3-C.sub.6)-cycloalkoxy, phenyl, heteroaryl, heterocyclyl, phenoxy, heteroaryloxy or heterocyclyloxy, wherein each of the last-mentioned 11 residues is unsubstituted or is substituted by one or more residues from the group consisting of halogen, nitro, hydroxyl, cyano, NR.sup.13R.sup.14, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, and wherein heterocyclyl has q oxo groups, R.sup.2 is hydrogen, (C.sub.1-C.sub.6)-alkyl, (C.sub.2-C.sub.6)-alkenyl, (C.sub.2-C.sub.6)-alkynyl, (C.sub.1-C.sub.4)-alkylsulphonyl, (C.sub.1-C.sub.4)-haloalkylsulphonyl, (C.sub.1-C.sub.6)-alkylcarbonyl, (C.sub.2-C.sub.6)-alkenylcarbonyl, (C.sub.2-C.sub.6)-alkynylcarbonyl, (C.sub.1-C.sub.6)-alkoxycarbonyl, di((C.sub.1-C.sub.6)-alkyl)aminocarbonyl, (C.sub.3-C.sub.8)-cycloalkylcarbonyl, heteroarylcarbonyl or phenylcarbonyl, wherein each of the last-mentioned 3 residues is unsubstituted or is substituted by one or more residues from the group consisting of halogen, nitro, cyano, NR.sup.13R.sup.14, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, R.sup.3 is halogen, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.2-C.sub.4)-alkynyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, methylthio, (C.sub.3-C.sub.8)-cycloalkyl, phenyl, phenyloxy, wherein each of the last-mentioned 3 residues is unsubstituted or is substituted by one or more residues from the group consisting of halogen, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, R.sup.4, R.sup.5 are each independently hydrogen, (C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.6)-haloalkyl, (C.sub.2-C.sub.6)-alkenyl, (C.sub.2-C.sub.6)-alkynyl, (C.sub.1-C.sub.6)-alkoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.6)-alkoxy-(C.sub.1-C.sub.3)-alkylcarbonyl, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-haloalkylthio, (C.sub.1-C.sub.4)-alkylthiocarbonyl, (C.sub.1-C.sub.4)-haloalkylthiocarbonyl, (C.sub.1-C.sub.4)-alkylthio-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylsulphoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylsulphonyl-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylthio-(C.sub.1-C.sub.3)-alkylcarbonyl, (C.sub.1-C.sub.4)-alkylsulphoxy-(C.sub.1-C.sub.3)-alkylcarbonyl, (C.sub.1-C.sub.4)-alkylsulphonyl-(C.sub.1-C.sub.3)-alkylcarbonyl, (C.sub.1-C.sub.6)-alkylcarbonyl, (C.sub.1-C.sub.6)-haloalkylcarbonyl, (C.sub.2-C.sub.6)-alkenylcarbonyl, (C.sub.2-C.sub.6)-alkynylcarbonyl, (C.sub.1-C.sub.6)-alkoxycarbonylcarbonyl, (C.sub.1-C.sub.6)-alkoxycarbonyl-(C.sub.1-C.sub.3)-alkylcarbonyl, (C.sub.1-C.sub.6)-alkoxycarbonyl, (C.sub.1-C.sub.6)-haloalkoxycarbonyl, (C.sub.2-C.sub.6)-alkenyloxycarbonyl, (C.sub.3-C.sub.6)-cycloalkyl, (C.sub.3-C.sub.6)-cycloalkyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.3-C.sub.6)-cycloalkylcarbonyl, (C.sub.3-C.sub.6)-cycloalkyl-(C.sub.1-C.sub.6)-alkylcarbonyl, phenyl, phenyl-(C.sub.1-C.sub.3)-alkyl, heteroaryl, heteroaryl-(C.sub.1-C.sub.3)-alkyl, heterocyclyl, heterocyclyl-(C.sub.1-C.sub.3)-alkyl, phenylcarbonyl, phenyl-(C.sub.1-C.sub.6)-alkylcarbonyl, hetarylcarbonyl, hetaryl-(C.sub.1-C.sub.6)-alkylcarbonyl, heterocyclylcarbonyl, heterocyclyl-(C.sub.1-C.sub.6)-alkylcarbonyl, wherein each of the last-mentioned 16 residues is unsubstituted or is substituted by one or more residues from the group consisting of halogen, nitro, hydroxyl, cyano, NR.sup.13R.sup.14, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, and wherein heterocyclyl has q oxo groups, wherein R.sup.4 and R.sup.5 are not both an alkyl residue, or NR.sup.4R.sup.5 is NCR.sup.8R.sup.9 or NS(O).sub.nR.sup.10R.sup.11, R.sup.6, R.sup.7 are each independently hydrogen or (C.sub.1-C.sub.4)-alkyl, R.sup.8, R.sup.9 are each independently hydrogen, (C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.6)-haloalkyl, (C.sub.2-C.sub.6)-alkenyl, (C.sub.2-C.sub.6)-alkynyl, (C.sub.1-C.sub.6)-alkoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylthio-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylsulphoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylsulphonyl-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.6)-alkoxy, (C.sub.1-C.sub.6)-haloalkoxy, (C.sub.2-C.sub.6)-alkenyloxy, NR.sup.13R.sup.14, (C.sub.3-C.sub.8)-cycloalkyl, (C.sub.3-C.sub.8)-cycloalkyl-(C.sub.1-C.sub.6)-alkyl, phenyl, phenyl-(C.sub.1-C.sub.3)-alkyl, heteroaryl, heteroaryl-(C.sub.1-C.sub.3)-alkyl, heterocyclyl, heterocyclyl-(C.sub.1-C.sub.3)-alkyl, wherein each of the last-mentioned 8 residues is unsubstituted or is substituted by one or more residues from the group consisting of halogen, nitro, hydroxyl, cyano, NR.sup.13R.sup.14, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, and wherein heterocyclyl has q oxo groups, or R.sup.8 and R.sup.9, together with the carbon atom to which they are attached, form a 3- to 6-membered unsaturated, partially saturated or saturated ring, which comprises in each case, in addition to the carbon atoms, p ring members from the group consisting of N(R.sup.12).sub.m, O and S(O).sub.n, and wherein said ring is unsubstituted or is substituted by one or more residues from the group consisting of halogen, nitro, hydroxyl, cyano, NR.sup.13R.sup.14, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, and wherein heterocyclyl has q oxo groups, R.sup.10, R.sup.11 are each independently, (C.sub.1-C.sub.6)-alkyl, (C.sub.2-C.sub.6)-alkenyl, (C.sub.2-C.sub.6)-alkynyl, (C.sub.1-C.sub.6)-alkoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylthio-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylsulphoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylsulphonyl-(C.sub.1-C.sub.3)-alkyl, (C.sub.3-C.sub.8)-cycloalkyl, (C.sub.3-C.sub.8)-cycloalkyl-(C.sub.1-C.sub.6)-alkyl, phenyl, phenyl-(C.sub.1-C.sub.3)-alkyl, heteroaryl, heteroaryl-(C.sub.1-C.sub.3)-alkyl, heterocyclyl, heterocyclyl-(C.sub.1-C.sub.3)-alkyl, wherein each of the last-mentioned 8 residues is unsubstituted or is substituted by one or more residues from the group consisting of halogen, nitro, hydroxyl, cyano, NR.sup.13R.sup.14, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, and wherein heterocyclyl has q oxo groups, or R.sup.10 and R.sup.11, together with the sulphur atom to which they are attached, form a 3- to 6-membered unsaturated, partially saturated or saturated ring, which comprises in each case, in addition to the carbon atoms and in addition to the sulphur atom, p ring members from the group consisting of N(R.sup.12).sub.m, O and S(O).sub.n, and wherein said ring is unsubstituted or is substituted by one or more residues from the group consisting of halogen, nitro, hydroxyl, cyano, NR.sup.13R.sup.14, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy or (C.sub.1-C.sub.4)-alkylsulphonyl, and wherein heterocyclyl has q oxo groups, R.sup.12 is hydrogen, (C.sub.1-C.sub.6)-alkyl or (C.sub.1-C.sub.6)-alkylcarbonyl, R.sup.13, R.sup.14 are each independently hydrogen, (C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.6)-alkylcarbonyl, (C.sub.1-C.sub.4)-alkylsulphonyl, phenyl, phenylcarbonyl, wherein each of the last-mentioned two residues is unsubstituted or is substituted by one or more residues from the group consisting of halogen, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, or R.sup.13 and R.sup.14, together with the nitrogen atom to which they are attached, form a 3- to 8-membered unsaturated, partially saturated or saturated ring, which comprises in each case, in addition to the carbon atoms and in addition to the nitrogen atom, p ring members from the group consisting of N(R.sup.12).sub.m, O and S(O).sub.n, and wherein said ring is unsubstituted or is substituted by one or more residues from the group consisting of halogen, hydroxyl, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, and has q oxo groups, n is independently selected from 0, 1 or 2, m is independently selected from 0 or 1, p is independently selected from 0, 1 or 2, q is independently selected from 0 or 1, y is 0 or 1, with the proviso that: y is 1, if R.sup.1 is a substituted phenyl residue or a substituted pyridin-3-yl residue.

    5. Compound of the formula (G) according to claim 2, and/or a salt thereof, in which A is CR.sup.6R.sup.7, W is O or S, R.sup.1 is (C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.6)-haloalkyl, (C.sub.2-C.sub.6)-alkenyl, (C.sub.2-C.sub.6)-alkynyl, NR.sup.13R.sup.14, R.sup.13R.sup.14N(C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.6)-alkoxy, (C.sub.1-C.sub.6)-haloalkoxy, (C.sub.1-C.sub.6)-alkoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.6)-alkoxy-(C.sub.2-C.sub.6)-alkoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, (C.sub.1-C.sub.4)-alkylthio-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylsulphoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylsulphonyl-(C.sub.1-C.sub.3)-alkyl, (C.sub.3-C.sub.6)-cycloalkyl, (C.sub.3-C.sub.6)-cycloalkenyl, (C.sub.3-C.sub.6)-cycloalkyl-(C.sub.1-C.sub.3)-alkyl, (C.sub.3-C.sub.6)-cycloalkenyl-(C.sub.1-C.sub.3)-alkyl, (C.sub.3-C.sub.6)-cycloalkoxy, phenyl, heteroaryl, heterocyclyl, phenoxy, heteroaryloxy or heterocyclyloxy, wherein each of the last-mentioned 11 residues is unsubstituted or is substituted by one or more residues from the group consisting of halogen, nitro, hydroxyl, cyano, NR.sup.13R.sup.14, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, and wherein heterocyclyl has q oxo groups, R.sup.2 is hydrogen, (C.sub.1-C.sub.6)-alkylcarbonyl, (C.sub.2-C.sub.6)-alkenylcarbonyl, (C.sub.2-C.sub.6)-alkynylcarbonyl, (C.sub.1-C.sub.6)-alkoxycarbonyl, (C.sub.3-C.sub.6)-cycloalkylcarbonyl, heteroarylcarbonyl, or phenylcarbonyl, wherein each of the last-mentioned 3 residues is unsubstituted or is substituted by one or more residues from the group consisting of halogen, nitro, cyano, NR.sup.13R.sup.14, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, R.sup.3 is halogen, methyl, difluoromethyl (CHF.sub.2), trifluoromethyl (CF.sub.3) or (C.sub.2-C.sub.3)-alkynyl, R.sup.4, R.sup.5 are each independently hydrogen, (C.sub.2-C.sub.6)-alkynyl, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-haloalkylthio, (C.sub.1-C.sub.4)-alkylthiocarbonyl, (C.sub.1-C.sub.4)-haloalkylthiocarbonyl, (C.sub.1-C.sub.6)-alkoxy-(C.sub.1-C.sub.3)-alkylcarbonyl, (C.sub.1-C.sub.4)-alkylthio-(C.sub.1-C.sub.3)-alkylcarbonyl, (C.sub.1-C.sub.4)-alkylsulphoxy-(C.sub.1-C.sub.3)-alkylcarbonyl, (C.sub.1-C.sub.4)-alkylsulphonyl-(C.sub.1-C.sub.3)-alkylcarbonyl, (C.sub.1-C.sub.6)-alkylcarbonyl, (C.sub.1-C.sub.6)-haloalkylcarbonyl, (C.sub.2-C.sub.6)-alkenylcarbonyl, (C.sub.2-C.sub.6)-alkynylcarbonyl, (C.sub.1-C.sub.6)-alkoxycarbonylcarbonyl, (C.sub.1-C.sub.6)-alkoxycarbonyl-(C.sub.1-C.sub.3)-alkylcarbonyl, (C.sub.1-C.sub.6)-alkoxycarbonyl, (C.sub.1-C.sub.6)-haloalkoxycarbonyl, (C.sub.2-C.sub.6)-alkenyloxycarbonyl, (C.sub.3-C.sub.6)-cycloalkylcarbonyl, (C.sub.3-C.sub.6)-cycloalkyl-(C.sub.1-C.sub.6)-alkylcarbonyl, phenylcarbonyl, phenyl-(C.sub.1-C.sub.6)-alkylcarbonyl, hetarylcarbonyl, hetaryl-(C.sub.1-C.sub.6)-alkylcarbonyl, heterocyclylcarbonyl, heterocyclyl-(C.sub.1-C.sub.6)-alkylcarbonyl, wherein each of the last-mentioned 8 residues is unsubstituted or is substituted by one or more residues from the group consisting of halogen, nitro, hydroxyl, cyano, NR.sup.13R.sup.14, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, and wherein heterocyclyl has q oxo groups, or NR.sup.4R.sup.5 is NCR.sup.8R.sup.9 or NS(O).sub.nR.sup.10R.sup.11, R.sup.6 is hydrogen, R.sup.7 is hydrogen or methyl, R.sup.8, R.sup.9 are each independently hydrogen, (C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.6)-haloalkyl, (C.sub.2-C.sub.6)-alkenyl, (C.sub.2-C.sub.6)-alkynyl, (C.sub.1-C.sub.6)-alkoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylthio-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylsulphoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylsulphonyl-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.6)-alkoxy, (C.sub.1-C.sub.6)-haloalkoxy, (C.sub.2-C.sub.6)-alkenyloxy, NR.sup.13R.sup.14, (C.sub.3-C.sub.8)-cycloalkyl, (C.sub.3-C.sub.8)-cycloalkyl-(C.sub.1-C.sub.6)-alkyl, phenyl, phenyl-(C.sub.1-C.sub.3)-alkyl, heteroaryl, heteroaryl-(C.sub.1-C.sub.3)-alkyl, heterocyclyl, heterocyclyl-(C.sub.1-C.sub.3)-alkyl, wherein each of the last-mentioned 8 residues is unsubstituted or is substituted by one or more residues from the group consisting of halogen, nitro, hydroxyl, cyano, NR.sup.13R.sup.14, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, and wherein heterocyclyl has q oxo groups, or R.sup.8 and R.sup.9, together with the carbon atom to which they are attached, form a 3- to 6-membered unsaturated, partially saturated or saturated ring, which comprises in each case, in addition to the carbon atoms, p ring members from the group consisting of N(R.sup.12).sub.m, O and S(O).sub.n, and wherein said ring is unsubstituted or is substituted by one or more residues from the group consisting of halogen, nitro, hydroxyl, cyano, NR.sup.13R.sup.14, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, and wherein heterocyclyl has q oxo groups, R.sup.10, R.sup.11 are each independently, (C.sub.1-C.sub.6)-alkyl, (C.sub.2-C.sub.6)-alkenyl, (C.sub.2-C.sub.6)-alkynyl, (C.sub.1-C.sub.6)-alkoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylthio-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylsulphoxy-(C.sub.1-C.sub.3)-alkyl, (C.sub.1-C.sub.4)-alkylsulphonyl-(C.sub.1-C.sub.3)-alkyl, (C.sub.3-C.sub.8)-cycloalkyl, (C.sub.3-C.sub.8)-cycloalkyl-(C.sub.1-C.sub.6)-alkyl, phenyl, phenyl-(C.sub.1-C.sub.3)-alkyl, heteroaryl, heteroaryl-(C.sub.1-C.sub.3)-alkyl, heterocyclyl, heterocyclyl-(C.sub.1-C.sub.3)-alkyl, wherein each of the last-mentioned 8 residues is unsubstituted or is substituted by one or more residues from the group consisting of halogen, nitro, hydroxyl, cyano, NR.sup.13R.sup.14, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, and wherein heterocyclyl has q oxo groups, or R.sup.10 and R.sup.11, together with the sulphur atom to which they are attached, form a 3- to 6-membered unsaturated, partially saturated or saturated ring, which comprises in each case, in addition to the carbon atoms and in addition to the sulphur atom, p ring members from the group consisting of N(R.sup.12).sub.m, O and S(O).sub.n, and wherein said ring is unsubstituted or is substituted by one or more residues from the group consisting of halogen, nitro, hydroxyl, cyano, NR.sup.13R.sup.14, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy or (C.sub.1-C.sub.4)-alkylsulphonyl, and wherein heterocyclyl has q oxo groups, R.sup.12 is hydrogen, (C.sub.1-C.sub.6)-alkyl or (C.sub.1-C.sub.6)-alkylcarbonyl, R.sup.13, R.sup.14 are each independently hydrogen, (C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.6)-alkylcarbonyl, (C.sub.1-C.sub.4)-alkylsulphonyl, phenyl, phenylcarbonyl, wherein each of the last-mentioned two residues is unsubstituted or is substituted by one or more residues from the group consisting of halogen, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, or R.sup.13 and R.sup.14, together with the nitrogen atom to which they are attached, form a 3- to 8-membered unsaturated, partially saturated or saturated ring, which comprises in each case, in addition to the carbon atoms and in addition to the nitrogen atom, p ring members from the group consisting of N(R.sup.12).sub.m, O and S(O).sub.n, and wherein said ring is unsubstituted or is substituted by one or more residues from the group consisting of halogen, hydroxyl, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, and has q oxo groups, n is independently selected from 0, 1 or 2, m is independently selected from 0 or 1, p is independently selected from 0, 1 or 2, q is independently selected from 0 or 1, y is 0 or 1, with the proviso that: y is 1, if R.sup.1 is a substituted phenyl residue or a substituted pyridin-3-yl residue.

    6. Compound of the formula (G) according to claim 2, and/or a salt thereof, in which R.sup.3 is halogen, trifluoromethyl or ethynyl.

    7. Compound of the formula (G) according to claim 2, and/or a salt thereof, in which y is 1.

    8. Compound of the formula (G) according to claim 2, and/or a salt thereof, in which n is independently selected from 0, 1 or 2, optionally independently selected from 0 or 1, m is independently selected from 0 or 1, optionally m is 0, p is independently selected from 0, 1 or 2, optionally p is independently selected from 0 or 1, and q is independently selected from 0 or 1, optionally q is 0.

    9. A product that is a herbicide and/or plant growth regular comprising a compound and/or salt according to claim 2.

    10. Herbicidal and/or plant growth-regulating composition, comprising one or more compounds of the formula (G) and/or salts thereof as defined in claim 2, and one or more further substances selected from groups (i) and/or (ii): (i) one or more further agrochemically active substances, optionally selected from the group consisting of insecticides, acaricides, nematicides, further herbicides, fungicides, safeners, fertilizers and/or further growth regulators, (ii) one or more formulation auxiliaries customary in crop protection.

    11. Method for controlling harmful plants or for regulating the growth of plants, comprising applying an effective amount of a product comprising one or more compounds of the formula (G) and/or salts thereof, as defined in claim 1. to the plants, seeds of plants, soil in which or on which plants grow and/or an area under cultivation.

    12. Compound of the formula (Z-A), (Z-B) and/or a salt thereof, ##STR00025## wherein Q is hydrogen, CN, COCl, COF, CO.sub.2H and salts thereof, CONR.sup.13R.sup.14, and CO.sub.2R.sup.q, wherein R.sup.q is (C.sub.1-C.sub.9)-alkyl or (C.sub.1-C.sub.9)-haloalkyl, R.sup.Z8 is selected from the group consisting of H, F, Cl, Br, I, CH.sub.3, CH.sub.2F, CHF.sub.2 and CF.sub.3, R.sup.Z1 and R.sup.Z2 are each independently hydrogen, CN, CH.sub.2aryl, XC(Y), wherein Y is NH, O or S and X is NH.sub.2, OH, SH, (C.sub.1-C.sub.8)-alkyl, (C.sub.1-C.sub.8)-haloalkyl, (C.sub.1-C.sub.8)-alkoxy, (C.sub.1-C.sub.8)-haloalkoxy, (C.sub.1-C.sub.6)-alkylthio, HN(C.sub.1-C.sub.8)-alkyl, or aryl, wherein each aryl is unsubstituted or is substituted by one or more residues from the group consisting of halogen, nitro, hydroxyl, cyano, NR.sup.13R.sup.14, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, and (C.sub.1-C.sub.4)-alkylsulphonyl, R.sup.Z3 is hydrogen, (C.sub.1-C.sub.8)-alkyl, (C.sub.1-C.sub.8)-haloalkyl, (C.sub.1-C.sub.8)-alkoxy, (C.sub.1-C.sub.8)-haloalkoxy, (C.sub.1-C.sub.6)-alkylthio, or aryl, wherein aryl is unsubstituted or is substituted by one or more residues from the group consisting of halogen, nitro, hydroxyl, cyano, NR.sup.13R.sup.14, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, and (C.sub.1-C.sub.4)-alkylsulphonyl, R.sup.Z4 is (C.sub.1-C.sub.8)-alkyl, (C.sub.1-C.sub.8)-haloalkyl, (C.sub.1-C.sub.8)-alkoxy, (C.sub.1-C.sub.8)-haloalkoxy, (C.sub.1-C.sub.6)-alkylthio, or aryl, wherein aryl is unsubstituted or is substituted by one or more residues from the group consisting of halogen, nitro, hydroxyl, cyano, NR.sup.13R.sup.14, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, and (C.sub.1-C.sub.4)-alkylsulphonyl, wherein R.sup.13 and R.sup.14 in each case each independently hydrogen, (C.sub.1-C.sub.12)-alkyl, (C.sub.1-C.sub.12)-haloalkyl, (C.sub.2-C.sub.12)-alkenyl, (C.sub.2-C.sub.12)-haloalkenyl, (C.sub.2-C.sub.12)-alkynyl, (C.sub.2-C.sub.12)-haloalkynyl, (C.sub.1-C.sub.12)-alkylcarbonyl, (C.sub.2-C.sub.12)-alkenylcarbonyl, (C.sub.2-C.sub.12)-alkynylcarbonyl, (C.sub.1-C.sub.12)-haloalkylcarbonyl, (C.sub.1-C.sub.4)-alkylsulphonyl, (C.sub.3-C.sub.8)-cycloalkyl, (C.sub.3-C.sub.8)-cycloalkenyl, (C.sub.3-C.sub.8)-cycloalkyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.3-C.sub.8)-cycloalkenyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.3-C.sub.8)-cycloalkylcarbonyl, (C.sub.3-C.sub.8)-cycloalkenylcarbonyl, (C.sub.3-C.sub.8)-cycloalkyl-(C.sub.1-C.sub.6)-alkylcarbonyl, (C.sub.3-C.sub.8)-cycloalkenyl-(C.sub.1-C.sub.6)-alkylcarbonyl, aryl, arylcarbonyl, arylsulphonyl, hetaryl, hetarylcarbonyl, hetarylsulphonyl, heterocyclyl, heterocyclylcarbonyl, heterocyclylsulphonyl, wherein each of the last-mentioned 17 residues is unsubstituted or is substituted by one or more residues from the group consisting of halogen, nitro, hydroxyl, cyano, NH.sub.2, (C.sub.1-C.sub.6)-alkylamine, (C.sub.1-C.sub.6)-dialkylamine, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, (C.sub.1-C.sub.4)-haloalkylthio, (C.sub.1-C.sub.6)-haloalkylsulphoxy, (C.sub.1-C.sub.4)-haloalkylsulphonyl, (C.sub.1-C.sub.4)-alkoxycarbonyl, (C.sub.1-C.sub.4)-haloalkoxycarbonyl, (C.sub.1-C.sub.4)-alkylcarboxy, (C.sub.3-C.sub.8)-cycloalkyl, (C.sub.3-C.sub.8)-cycloalkyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.4)-alkoxycarbonyl-(C.sub.1-C.sub.4)-alkyl, hydroxycarbonyl, hydroxycarbonyl-(C.sub.1-C.sub.4)-alkyl and wherein heterocyclyl has q oxo groups, or R.sup.13 and R.sup.14, together with the nitrogen atom to which they are attached, form a 3- to 8-membered unsaturated, partially saturated or saturated ring, which comprises in each case, in addition to the carbon atoms and in addition to the nitrogen atom, p ring members from the group consisting of N(R.sup.12).sub.m, O and S(O).sub.n and wherein said ring is unsubstituted or is substituted by one or more residues from the group consisting of halogen, nitro, hydroxyl, cyano, NH.sub.2, (C.sub.1-C.sub.6)-alkylamine, (C.sub.1-C.sub.6)-dialkylamine, (C.sub.1-C.sub.4)-alkyl, (C.sub.1-C.sub.4)-haloalkyl, (C.sub.1-C.sub.4)-alkoxy, (C.sub.1-C.sub.4)-haloalkoxy, (C.sub.1-C.sub.4)-alkylthio, (C.sub.1-C.sub.4)-alkylsulphoxy, (C.sub.1-C.sub.4)-alkylsulphonyl, (C.sub.1-C.sub.4)-haloalkylthio, (C.sub.1-C.sub.4)-haloalkylsulphoxy, (C.sub.1-C.sub.4)-haloalkylsulphonyl, (C.sub.1-C.sub.4)-alkoxycarbonyl, (C.sub.1-C.sub.4)-haloalkoxycarbonyl, (C.sub.1-C.sub.4)-alkylcarboxy, (C.sub.3-C.sub.6)-cycloalkyl, (C.sub.3-C.sub.6)-cycloalkyl-(C.sub.1-C.sub.6)-alkyl, (C.sub.1-C.sub.4)-alkoxycarbonyl-(C.sub.1-C.sub.4)-alkyl, hydroxycarbonyl, hydroxycarbonyl-(C.sub.1-C.sub.4)-alkyl and has q oxo groups, n is independently selected from 0, 1 or 2, m is independently selected from 0 or 1, p is independently selected from 0, 1, 2 or 3, q is independently selected from 0, 1 or 2, y is 0 or 1.

    13. Compound of the formula (Z-1), (Z-2), (Z-3), (Z-4), (Z-5), (Z-6) and/or a salt thereof, ##STR00026## ##STR00027## wherein A.sup.1 is selected from the group consisting of H, F, Cl, Br and I, A.sup.2 is selected from the group consisting of F, Cl, Br and I, A.sup.3 is H or C.sub.1, A.sup.4 is H or Br, E.sup.1 is selected from the group consisting of H, methyl, ethyl and iso-propyl, E.sup.2 is selected from the group consisting of H, methyl, ethyl, iso-propyl, and tert-butyl.

    14. Process for preparing a compound of the formula (G) as defined in claim 2, and/or a salt thereof, comprising obtaining (a) a compound of formula (G) wherein W is oxygen in a chemical synthesis comprising reacting a compound of formula (E-II) ##STR00028## in which R.sup.1, R.sup.2, R.sup.3, A and y each have the meaning as defined in formula (G), and wherein R.sup.3 optionally represents a halogen atom, with HNR.sup.4R.sup.5, wherein R.sup.4 and R.sup.5 each have the meaning as defined in formula (G), or (b) a compound of formula (G) wherein W is oxygen is obtained in a chemical synthesis comprising reacting a compound of the formula (E-VIII) or of the formula (E-XXVII) ##STR00029## in which R.sup.3 has the meaning as defined in formula (G), and wherein R.sup.4 and R.sup.5 each have the meaning as defined in formula (G), with a compound of formula (E-XXXII) ##STR00030## wherein y, A, R.sup.1 and R.sup.2 each have the meaning as defined in formula (G), or (c) a compound of formula (G), wherein W is sulphur is obtained in a chemical synthesis comprising reacting a compound of the formula (E-V) ##STR00031## in which R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, A and y each have the meaning as defined in formula (G), and wherein R.sup.3 preferably represents a halogen atom, with a thionation agent.

    Description

    EXAMPLES

    [0434] In an exemplary manner, some synthesis examples of compounds of the general formula (G) are described below. In the examples, the amounts (including percentages) refer to the weight, unless especially stated otherwise.

    [0435] The symbols > and < mean greater than and smaller than, respectively. The symbol means greater than or equal to, the symbol means smaller than or equal to.

    [0436] If, in the context of the description and the examples, the terms R and S are given for the absolute configuration on a centre of chirality of the stereoisomers of the formula (G), this RS nomenclature follows, unless defined differently, the Cahn-Ingold-Prelog rule.

    [0437] In the context of the present invention and in the Tables 1 to 5 mentioning specific and preferred compounds according to the present invention, the following abbreviations are used: [0438] H=hydrogen [0439] Me=methyl or CH.sub.3 [0440] Et=ethyl [0441] Pr=propyl [0442] Bu=butyl [0443] nAlkyl=n-alkyl, e.g. nPr=n-propyl [0444] cAlkyl=cycloalkyl, e.g. cPr=cyclopropyl, cHexyl=cyclohexyl [0445] iAlkyl=isooalkyl, e.g. iPr=isopropyl [0446] tAlkyl=tertiary alkyl, e.g. tBu=tert-butyl [0447] F, Cl, Br, I=fluorine, chlorine, bromine and iodine, respectively, in accordance with the conventional chemical atom symbol [0448] MeO or OMe=methoxy [0449] CN=cyano [0450] NO.sub.2=nitro [0451] Ph=phenyl [0452] diHal=diHal, e.g. diF=difluoro [0453] triHal=triHal, e.g. triF=trifluoro [0454] CCH=ethinyl (CCH)

    [0455] The position of a substituent, e.g. at the phenyl ring in position 2, is stated as a prefix to the symbol or the abbreviation of the radical, for example [0456] 2-Cl=2-chloro [0457] 2-Me=2-methyl

    [0458] Numerations of the substituent positions for di- or trisubstituted substitution patterns are analogously stated as a prefix, for example [0459] 2,3-Cl.sub.2=2,3-dichloro (e.g. as substitution at the phenyl ring) [0460] 2,4-diF=2,4-difluoro (e.g. as substitution at the phenyl ring) [0461] 2,4-F.sub.2=2,4-difluoro (e.g. as substitution at the phenyl ring) [0462] 2,4,6-triF=2,4,6-trifluoro (e.g. as substitution at the phenyl ring) [0463] 2-F-4-Cl=2-fluoro, 4-chloro (e.g. as substitution at the phenyl ring) [0464] 5-F-2-Me=5-fluoro, 2-methyl (e.g. as substitution at the phenyl ring)

    [0465] Other abbreviations are to be understood analogously to the examples stated above.

    [0466] In addition, the customary chemical symbols and formulae apply, such as, for example, CH.sub.2 for methylene or CF.sub.3 for trifluoromethyl or OH for hydroxyl.

    [0467] Correspondingly, composite meanings are defined as composed of the abbreviations mentioned, for example [0468] 4-CF.sub.3-cHexyl=4-trifluoromethyl-cyclohexyl

    [0469] NMR-Peak lists

    [0470] 1H-NMR data of selected examples are written in form of 1H-NMR-peak lists. To each signal peak are listed the -value in ppm and the signal intensity in round brackets. Between the -value-signal intensity pairs are semicolons as delimiters.

    [0471] The peak list of an example has therefore the form:

    [0472] 1 (intensity1); 2 (intensity2); . . . ; i (intensityi); . . . ; n (intensityn)

    [0473] Intensity of sharp signals correlates with the height of the signals in a printed example of a NMR spectrum in cm and shows the real relations of signal intensities. From broad signals several peaks or the middle of the signal and their relative intensity in comparison to the most intensive signal in the spectrum can be shown.

    [0474] For calibrating chemical shift for 1H spectra, tetramethylsilane and/or the chemical shift of the solvent was used, especially in the case of spectra measured in DMSO (Dimethyl sulfoxide). Therefore in NMR peak lists, tetramethylsilane peak can occur, but not necessarily

    [0475] The 1H-NMR peak lists are similar to classical 1H-NMR prints and contains therefore usually all peaks, which are listed at classical NMR-interpretation.

    [0476] Additionally they can show like classical 1H-NMR prints signals of solvents, stereoisomers of the target compounds, which are also object of the invention, and/or peaks of impurities.

    [0477] To show compound signals in the delta-range of solvents and/or water the usual peaks of solvents, for example peaks of DMSO in DMSO-D.sub.6 and the peak of water are shown in our 1H-NMR peak lists and have usually on average a high intensity.

    [0478] The peaks of stereoisomers of the target compounds and/or peaks of impurities have usually on average a lower intensity than the peaks of target compounds (for example with a purity >90%).

    [0479] Such stereoisomers and/or impurities can be typical for the specific preparation process. Therefore their peaks can help to recognize the reproduction of our preparation process via side-products-fingerprints.

    [0480] An expert, who calculates the peaks of the target compounds with known methods (MestreC, ACD-simulation, but also with empirically evaluated expectation values) can isolate the peaks of the target compounds as needed optionally using additional intensity filters. This isolation would be similar to relevant peak picking at classical 1H-NMR interpretation.

    [0481] Further details of NMR-data description with peak lists can be found in the publication Citation of NMR Peaklist Data within Patent Applications of the Research Disclosure Database Number 564025.

    [0482] The compounds according to the present invention, such as described in the Tables 1 to 5, are obtained according to or analogously to the following chemical synthesis examples.

    [0483] (A) Chemical synthesis examples:

    1. Synthesis of 3-amino-4-chloro-N-(cyclohexylmethyl)isothiazole-5-carboxamide (I-4)

    1.1. Synthesis of 3,4-dichloro-N-(cyclohexylmethyl)isothiazole-5-carboxamide

    [0484] 730 mg of 3,4-dichloroisothiazole-5-carboxylic acid (3.7 mmol) were dissolved in 10 ml of dichloromethane and a drop of dimethylformamide was added. 1.4 g of oxalyl chloride (11.1 mmol) were added dropwise at room temperature. After stirring for 1 h at room temperature, the solution was evaporated to dryness on a rotary evaporator. The residue was taken up in 3 ml of dichloromethane and slowly added dropwise to a solution of 626 mg of 1-cyclohexylmethanamine (5.5 mmol) and 746 mg of triethylamine (7.4 mmol) in 10 ml of dichloromethane. The mixture was stirred at room temperature for 1 h. The reaction mixture was then added to water and extracted repeatedly with dichloromethane. The concentrated extracts were dried over MgSO4, concentrated and purified by column chromatography. Yield: 1.05 g (97% of theory).

    [0485] .sup.1H-NMR (400 MHz, CDCl.sub.3 , ppm) 6.86 (br, 1H), 3.34 (tr, 2H), 1.77 (m, 4H), 1.66 (m, 1H), 1.58 (m, 1H), 1.3-1.15 (m, 3H), 1.0 (m, 2H).

    1.2. Synthesis of 4-chloro-N-(cyclohexylmethyl)-3-[(diphenylmethylene)amino]isothiazole-5-carboxamide

    [0486] 1.27 g of 3,4-dichloro-N-(cyclohexylmethyl)isothiazole-5-carboxamide (4.3 mmol) were dissolved in 6 ml of toluene. To this solution were added consecutively 1.87 g of benzophenone imine (10 mmol), 2.8 g of caesium carbonate (8.68 mmol), 102 mg of Xantphos (0.17 mmol) and 79 mg of tri(dibenzylideneacetone)dipalladium (Pd.sub.2dba.sub.3; 0.087 mmol). The reaction vessel with the resulting solution was then briefly evacuated and immediately filled with argon three times in succession. The mixture was then heated in an oil bath preheated to 100 C. for 24 h. After cooling, the reaction solution was added to water, extracted repeatedly with ethyl acetate, dried, concentrated and purified by column chromatography. Yield: 253 mg (13% of theory).

    [0487] .sup.1H-NMR (400 MHz, CDCl.sub.3 , ppm) 7.82 (d, 2H), 7.57-7.21 (m, 8H), 6.80 (br, 1H), 3.29 (tr, 2H), 1.76 (m, 4H), 1.67 (m, 1H), 1.58 (m, 1H), 1.3-1.15 (m, 3H), 1.04-0.95 (m, 2H).

    1.3. Synthesis of 3-amino-4-chloro-N-(cyclohexylmethyl)isothiazole-5-carboxamide (I-4)

    [0488] 184 mg of 4-chloro-N-(cyclohexylmethyl)-3-[(diphenylmethylene)amino]isothiazole-5-carboxamide were dissolved in 1.5 ml of tetrahydrofuran (THF) to which 0.5 ml of 6N hydrochloric acid was added and the mixture was stirred at room temperature until the reactant was completely consumed according to thin-layer chromatography. The reaction mixture was added to a little water and extracted with ethyl acetate. On drying the ethyl acetate phases, concentrating and chromatography, the desired product was obtained. Yield: 89 mg (77% of theory).

    [0489] .sup.1H-NMR (400 MHz, CDCl.sub.3 , ppm) 6.68 (br, 1H), 4.73 (br, 2H), 3.32 (tr, 2H), 1.77 (m, 4H), 1.66 (m, 1H), 1.57 (m, 1H), 1.32-1.13 (m, 3H), 1.06-0.96 (m, 2H).

    2. Synthesis of 3-amino-4-chloro-N-(3,4,5-trifluorobenzyl)isothiazole-5-carboxamide (I-35)

    2.1. Synthesis of ethyl 3,4-dichloroisothiazole-5-carboxylate

    [0490] 15 g of 3,4-dichloroisothiazole-5-carboxylic acid (75.7 mmol) were dissolved in 300 ml of ethanol and 8.4 ml of concentrated sulphuric acid were added. The mixture was stirred under reflux for 20 h. The reaction mixture was then concentrated to half the original volume, neutralized with saturated NaHCO.sub.3, added to water and extracted with dichloromethane. The dichloromethane phases were dried and carefully concentrated on a rotary evaporator. Yield: 15.2 g (89% of theory).

    [0491] .sup.1H-NMR (400 MHz, CDCl.sub.3 , ppm) 4.44 (q, 2H), 1.42 (tr, 3H).

    2.2. Synthesis of ethyl 4-chloro-3-[(diphenylmethylene)amino]isothiazole-5-carboxylate

    [0492] 14.06 g of ethyl 3,4-dichloroisothiazole-5-carboxylate (62.19 mmol) were dissolved in 150 ml of toluene. To this solution were added consecutively 13.9 g of benzophenone imine (74.6 mmol), 40.5 g caesium carbonate (124.4 mmol), 1.44 g Xantphos (2.49 mmol) and 1.14 g tri(dibenzylidenaceton)dipalladium (Pd.sub.2dba.sub.3; 1.24 mmol). The reaction vessel with the resulting solution was then briefly evacuated and immediately filled with argon three times in succession. The mixture was then heated for 24 h in an oil bath which had been preheated to 100 C. After cooling, the reaction solution was filtered through a 2 cm thick layer of silica gel, which was rinsed repeatedly with dichloromethane. The filtrate was concentrated and the residue purified by column chromatography. Yield: 5.29 g (23% of theory).

    [0493] .sup.1H-NMR (400 MHz, CDCl.sub.3 , ppm) 7.82 (d, 2H), 7.59-7.22 (m, 8H), 4.36 (q, 2H), 1.37 (tr, 3H).

    2.3. Synthesis of ethyl 3-amino-4-chloroisothiazole-5-carboxylate

    [0494] 10.1 g of ethyl 4-chloro-3-[(diphenylmethylene)amino]isothiazole-5-carboxylate (27.2 mmol) were dissolved in 200 ml of tetrahydrofuran (THF) to which 12 ml of 6N hydrochloric acid was added and the mixture was stirred at room temperature until the reactant was completely consumed according to thin-layer chromatography. The reaction mixture was added to a little water and extracted with ethyl acetate. On drying the ethyl acetate phases, concentrating and chromatography, the desired product was obtained. Yield: 4.51 g (91% of theory).

    [0495] .sup.1H-NMR (400 MHz, CDCl.sub.3 , ppm) 5.0-4.5 (br, 2H), 4.40 (q, 2H), 1.39 (tr, 3H).

    2.4. Synthesis of 3-amino-4-chloroisothiazole-5-carboxylic Acid

    [0496] To 4.27 g of ethyl 3-amino-4-chloroisothiazole-5-carboxylate (20.6 mmol) in a mixture of 50 ml of ethanol and 50 ml of THF were added 26 ml of 2N sodium hydroxide solution and the mixture was stirred at room temperature for 1 h. The reaction mixture was then adjusted to pH 5 by careful addition of 2N hydrochloric acid, whereupon a portion of the product precipitated in the form of crystals. The crystals were filtered off under suction and the filtrate was extracted with ethyl acetate. The organic extracts were dried and concentrated, whereby a further batch of the product was obtained. Yield: 3.57 g (97% of theory).

    [0497] .sup.1H-NMR (400 MHz, DMSO 6, ppm) 14.05 (br, 1H), 6.58 (s, 2H).

    2.5. Synthesis of 3-amino-4-chloro-N-(3,4,5-trifluorobenzyl)isothiazole-5-carboxamide (I-35)

    [0498] To 100 mg of 3-amino-4-chloroisothiazole-5-carboxylic acid (0.56 mmol) in 4 ml of dichloromethane were added 130 mg of 3,4,5-trifluorobenzylamine (0.78 mmol), 170 mg of triethylamine (1.68 mmol) and 0.83 ml of a 50 percent solution of n-propylphosphonic anhydride (T3P; 1.4 mmol) in THF and the mixture was stirred overnight at room temperature. The reaction mixture was then added to water and extracted repeatedly with ethyl acetate. The organic extracts were washed with saturated sodium chloride solution, dried and concentrated on a rotary evaporator. The residue was purified by column chromatography. Yield: 102 mg (57% of theory).

    [0499] .sup.1H-NMR (400 MHz, DMSO 6, ppm) 9.0 (tr, 1H), 7.26 (m, 2H), 6.56 (s, 2H), 4.43 (d, 2H).

    3. Synthesis of 3-amino-4-chloro-N-(2,4-difluorobenzyl)isothiazole-5-carbothioamide (IV-5)

    3.1. Synthesis of 3-amino-4-chloro-N-(2,4-difluorobenzyl)isothiazole-5-carboxamide (I-22)

    [0500] Analogously to the synthesis of compound 1-35 described above, 120 mg of 3-amino-4-chloroisothiazole-5-carboxylic acid (0.67 mmol) were reacted with 143 mg (1 mmol) of 2,4-difluorobenzylamine. Yield: 188 mg (91% of theory).

    [0501] .sup.1H-NMR (400 MHz, CDCl.sub.3 , ppm) 7.41 (m, 1H), 7.03 (br, 1H), 6.86 (m, 2H), 4.73 (br, 2H), 4.66 (d, 2H).

    3.2. Synthesis of 3-amino-4-chloro-N-(2,4-difluorobenzyl)isothiazole-5-carbothioamide (IV-5)

    [0502] 83 mg of 3-amino-4-chloro-N-(2,4-difluorobenzyl)isothiazole-5-carboxamide (0.27 mmol) and 121 mg of 4-methoxyphenyldithiophosphonic anhydride (Lawesson's reagent; 0.3 mmol) in 2 ml of THF were stirred at room temperature for 6 h and at 50 C. for 1 h. After cooling, the mixture was added to water and extracted with dichloromethane. The dichloromethane phases were dried and concentrated. The residue was purified by column chromatography. Yield: 17.1 mg (20% of theory).

    [0503] .sup.1H-NMR (400 MHz, CDCl.sub.3 , ppm) 8.67 (br, 1H), 7.48 (m, 1H), 6.90 (m, 2H), 5.02 (d, 2H).

    4. Synthesis of 4-chloro-N-(cyclohexylmethyl)-3-(pentanoylamino)isothiazole-5-carboxamide (II-233)

    [0504] To 70 mg of 3-amino-4-chloro-N-(cyclohexylmethyl)isothiazole-5-carboxamide (I-4; 0.25 mmol) in 3 ml of dichloromethane were added 52 mg of triethylamine (0.51 mmol), 4 mg of 4-dimethylaminopyridine and 62 mg of n-pentanoyl chloride (0.51 mmol) and the mixture was stirred for 3 h at room temperature. The mixture was then added to water and extracted with dichloromethane. The dichloromethane phases were dried and concentrated. The residue was purified by chromatography. Yield: 53 mg (57% of theory)

    [0505] .sup.1H-NMR (400 MHz, CDCl.sub.3 , ppm) 7.68 (bs, 1H), 6.73 (bs, 1H), 3.33 (t, 2H), 2.63 (bs, 2H), 1.73 (m, 6H), 1.59 (m, 2H), 1.43 (m, 2H), 1.21 (m, 4H), 1.00 (m, 4H).

    5. Synthesis of 4-chloro-N-(2,6-difluorobenzyl)-3-[(trifluoroacetyl)amino]isothiazole-5-carboxamide (II-240

    5.1. Synthesis of 3-amino-4-chloro-N-(2,6-difluorobenzyl)isothiazole-5-carboxamide (I-24)

    [0506] Analogously to the synthesis of compound 1-35 described above, 100 mg of 3-amino-4-chloroisothiazole-5-carboxylic acid (0.56 mmol) were reacted with 115 mg of 2,6-difluorobenzylamine (0.78 mmol). Yield: 125 mg (74% of theory).

    [0507] .sup.1H-NMR (400 MHz, CDCl.sub.3 , ppm) 7.31 (m, 1H), 7.05 (bs, 1H), 6.94 (m, 2H), 4.76 (d, 2H), 4.72 (bs, 2H).

    5.2. Synthesis of 4-chloro-N-(2,6-difluorobenzyl)-3-[(trifluoroacetyl)amino]isothiazole-5-carboxamide (II-240)

    [0508] To 20 mg of 3-amino-4-chloro-N-(2,6-difluorobenzyl)isothiazole-5-carboxamide (I-24; 0.06 mmol) in 1 ml of dichloromethane were added 13 mg of triethylamine (0.13 mmol), 2 mg of 4-dimethylaminopyridine and 28 mg of trifluoroacetic anhydride (0.13 mmol) and the mixture was stirred for 3 h at room temperature. The mixture was then added to water and extracted with dichloromethane. The dichloromethane phases were dried and concentrated and the residue was purified by chromatography. Yield: 13 mg (49% of theory).

    [0509] .sup.1H-NMR (400 MHz, CDCl.sub.3 , ppm) 8.29 (bs, 1H), 7.31 (m, 1H), 7.09 (bs, 1H), 6.94 (m, 2H), 4.78 (d, 2H).

    6. Synthesis of 3-amino-4-chloro-N-[(1-chlorocyclopropyl)carbonyl]-N-(2,4-difluorobenzyl)isothiazole-5-carboxamide (V-11)

    [0510] To 80 mg of 3-amino-4-chloro-N-(2,4-difluorobenzyl)isothiazole-5-carboxamide (I-22; 0.26 mmol) in 4 ml of dichloromethane were added 53 mg of triethylamine (0.52 mmol), 4 mg of 4-dimethylaminopyridine and 73 mg of 1-chlorocyclopropanecarbonyl chloride (0.52 mmol) and the mixture was stirred for 2 h at room temperature. The mixture was then added to water and extracted with dichloromethane. The dichloromethane phases were dried and concentrated. The residue obtained therefrom was purified by chromatography. Yield: 24 mg (22% of theory).

    [0511] .sup.1H-NMR (400 MHz, CDCl.sub.3 , ppm) 7.37 (m, 1H), 6.83 (m, 2H), 5.06 (s, 2H), 4.82 (bs, 2H), 1.66 (m, 2H), 1.30 (m, 2H).

    7. Synthesis of 3-amino-N-(cyclohexylmethyl)-4-ethynylisothiazole-5-carboxamide (I-209)

    7.1. Synthesis of methyl 3-amino-4-[(trimethylsilyl)ethynyl]isothiazole-5-carboxylate

    [0512] To 650 mg (2.28 mmol) of methyl 3-amino-4-iodo-1,2-thiazole-5-carboxylate in 11 ml of DMF were added 43.6 mg (0.229 mmol) of CuI, 160 mg (0.229 mmol) of Pd(PPh.sub.3).sub.2Cl.sub.2 and 0.638 ml (5.58 mmol) of triethylamine and the mixture was stirred at room temperature for 5 min under protective gas (argon). 0.647 ml (4.58 mmol) of ethynyltrimethylsilane were added dropwise and then the mixture was stirred for 1 h at 100 C. The mixture was then concentrated on a rotary evaporator and the residue was treated with a saturated NH.sub.4Cl solution and extracted with dichloromethane/heptane 1:9. The organic phase was dried over Na.sub.2SO.sub.4, filtered and concentrated by rotary evaporation. The residue was purified by chromatography. Yield: 486 mg (83% of theory)

    [0513] .sup.1H-NMR (400 MHz, CDCl.sub.3 , ppm) 4.91 (br, 2H), 3.92 (s, 3H), 0.29 (s, 9H).

    7.2. Synthesis of 3-amino-4-ethynylisothiazole-5-carboxylic acid

    [0514] 300 mg (1.18 mmol) of methyl 3-amino-4-[(trimethylsilyl)ethynyl]isothiazole-5-carboxylate were dissolved in 10 ml of THF/methanol 1:1. 1.77 ml (3.54 mmol) of NaOH dissolved in 2 ml of water were added dropwise. After stirring for 1 h at room temperature, the mixture was concentrated on a rotary evaporator. The residue was treated with 2M HCl and the mixture was extracted with ethyl acetate. The organic phase was dried over Na.sub.2SO.sub.4, filtered and concentrated by rotary evaporation. Yield: 197 mg (100%) of crude product.

    7.3. Synthesis of 3-amino-N-(cyclohexylmethyl)-4-ethynylisothiazole-5-carboxamide (I-209)

    [0515] 135 mg (0.8 mmol) of 3-amino-4-ethynylisothiazole-5-carboxylic acid, 0.26 ml (2.0 mmol) of cyclohexylmethylamine, 1.27 g (2.0 mmol, 50% in THF) of n-propylphosphonic anhydride (T3P) and 0.335 ml (2.4 mmol) of triethylamine were dissolved in 8 ml of THF and the mixture was stirred at 55 C. for 1.5 h. The mixture was then concentrated on a rotary evaporator, the residue then treated with 2M NaOH and extracted repeatedly with ethyl acetate. The organic extracts were dried with Na.sub.2SO.sub.4 and concentrated on a rotary evaporator. The residue was purified by column chromatography. Yield: 156 mg (74% of theory).

    [0516] .sup.1H-NMR (400 MHz, CDCl.sub.3 , ppm) 7.12 (br, 1H), 4.83 (br, 2H), 3.77 (s, 1H), 3.32 (t, 2H), 1.80-1.56 (m, 6H), 1.31-1.15 (m, 3H), 1.06-1.00 (m, 2H).

    8. Synthesis of 3-amino-N-(cyclohexylmethyl)-4-ethylisothiazole-5-carboxamide (I-127)

    8.1. Synthesis of methyl 3-[(tert-butoxycarbonyl)amino]-4-vinylisothiazole-5-carboxylate

    [0517] 1.10 g (2.86 mmol) of methyl 3-[(tert-butoxycarbonyl)amino]-4-iodoisothiazole-5-carboxylate, 460 mg (3.44 mmol) of potassium trifluoro(vinyl)borate and 0.6 ml (4.30 mmol) of triethylamine were dissolved in 7.7 ml of ethanol and the mixture was stirred for 5 min at room temperature under protective gas (argon). 25.4 mg (0.143 mmol) of PdCl.sub.2 were added and the mixture was heated for 1 h at 100 C. in a microwave. The mixture was then concentrated and the residue extracted with NaHCO.sub.3 and ethyl acetate, separated off, dried with Na.sub.2SO.sub.4 and concentrated by rotary evaporation. The residue was purified by column chromatography. Yield: 580 mg (71% of theory).

    [0518] .sup.1H-NMR (400 MHz, CDCl.sub.3 , ppm) 7.16 (br, 1H), 7.10-7.02 (dd, 1H), 5.72-5.66 (m, 2H), 3.91 (s, 3H), 1.53 (s, 9H).

    8.2. Synthesis of 3-[(tert-butoxycarbonyl)amino]-4-vinylisothiazole-5-carboxylic acid

    [0519] 680 mg (2.39 mmol) of methyl 3-[(tert-butoxycarbonyl)amino]-4-vinylisothiazole-5-carboxylate were dissolved in 35 ml of THF. 2.63 ml of a 2M NaOH solution were added dropwise. After stirring for 2 h at room temperature, the mixture was concentrated on a rotary evaporator. The residue was treated with 2M HCl and extracted with ethyl acetate. The organic phase was dried over Na.sub.2SO.sub.4, filtered and concentrated by rotary evaporation. Yield: 645 mg (100%) of crude product.

    8.3. Synthesis of tert-butyl {5-[(cyclohexylmethyl)carbamoyl]-4-vinylisothiazol-3-yl}carbamate)

    [0520] 323 mg (1.20 mmol) of 3-[(tert-butoxycarbonyl)amino]-4-vinylisothiazole-5-carboxylic acid, 0.46 ml (3.59 mmol) of cyclohexylmethylamine, 950 mg (2.99 mmol, 50% in THF) of n-propylphosphonic anhydride (T3P) and 0.50 ml (3.59 mmol) of triethylamine were dissolved in 9 ml of THF and the mixture stirred at 55 C. for 1.5 h. The mixture was then concentrated on a rotary evaporator, the residue treated with 1M HCl and extracted repeatedly with dichloromethane. The organic extracts were dried with Na.sub.2SO.sub.4 and concentrated on a rotary evaporator. The residue was purified by column chromatography. Yield: 412 mg (94% of theory).

    [0521] .sup.1H-NMR (400 MHz, CDCl.sub.3 , ppm) 6.94 (br, 1H), 6.83-6.76 (dd, 1H), 6.16 (br, 1H), 5.76-5.65 (m, 2H), 3.25 (t, 2H), 1.74-1.68 (m, 4H), 1.54-1.47 (m, 11H), 1.36-1.11 (m, 3H), 1.01-0.88 (m, 2H).

    8.4. Synthesis of tert-butyl {5-[(cyclohexylmethyl)carbamoyl]-4-ethylisothiazol-3-yl}carbamate)

    [0522] 100 mg (0.274 mmol) of tert-butyl {5-[(cyclohexylmethyl)carbamoyl]-4-vinylisothiazol-3-yl}carbamate) were dissolved in 2.7 ml of methanol and 2.91 mg (0.027 mmol) of Pd/C (5%) were added. After stirring for 18 h at room temperature under hydrogen, the mixture was filtered and concentrated by rotary evaporation. Yield: 100 mg (99% of theory).

    [0523] .sup.1H-NMR (400 MHz, CDCl.sub.3 , ppm) 6.75 (br, 1H), 5.87 (br, 1H), 3.27 (t, 2H), 2.81 (q, 2H), 1.77-1.67 (m, 4H), 1.58-1.53 (m, 11H), 1.28-1.15 (m, 6H), 1.02-0.93 (m, 2H).

    8.5. Synthesis of 3-amino-N-(cyclohexylmethyl)-4-ethylisothiazole-5-carboxamide (I-127)

    [0524] 75 mg (0.204 mmol) of tert-butyl {5-[(cyclohexylmethyl)carbamoyl]-4-ethylisothiazol-3-yl}carbamate) and 0.204 ml (2.65 mmol) of TFA were together dissolved in 1 ml of dichloromethane and the mixture was stirred at room temperature for 30 min. The mixture was then concentrated on a rotary evaporator, the residue treated with 2M NaOH and extracted repeatedly with dichloromethane. The organic extracts were dried with Na.sub.2SO.sub.4 and concentrated on a rotary evaporator. The residue was purified by column chromatography.

    [0525] Yield: 51 mg (93% of theory).

    [0526] .sup.1H-NMR (400 MHz, CDCl.sub.3 , ppm) 5.82 (br, 1H), 4.52 (br, 2H), 3.25 (t, 2H), 2.74 (q, 2H), 1.76-1.53 (m, 6H), 1.27-1.15 (m, 6H), 1.02-0.88 (m, 2H).

    [0527] NMR Peak Lists

    [0528] NMR peak lists for compounds according to formula (G) in the context of the present invention. The numbering of these compounds (called Examples in said list) refers to Tables 1 to 5 above.

    TABLE-US-00006 Example I-10: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.522(0.7); 7.263(123.4); 6.999(0.7); 6.724(1.5); 4.772(5.5); 4.024(3.9); 4.021(4.1); 4.012(4.1); 3.995(4.4); 3.986(4.5); 3.429(4.8); 3.424(5.2); 3.404(11.0); 3.400(9.9); 3.394(9.8); 3.388(16.0); 3.372(12.6); 3.365(4.9); 3.316(0.8); 2.344(0.5); 2.334(0.7); 2.326(0.8); 2.315(0.6); 2.307(0.6); 2.080(1.9); 1.993(0.7); 1.964 (1.4); 1.956(0.6); 1.947(0.8); 1.938(0.8); 1.929(1.2); 1.917(1.4); 1.909(1.5); 1.900(2.4); 1.891(1.7); 1.883(1.4); 1.871 (1.5); 1.862(0.9); 1.854(0.8); 1.844(0.5); 1.694(4.0); 1.689(3.8); 1.684(3.1); 1.666(4.2); 1.661(5.2); 1.656(5.1); 1.449(2.1); 1.441(1.8); 1.438(2.2); 1.430(1.7); 1.419(4.3); 1.408(4.6); 1.386(4.1); 1.378(3.4); 1.375(3.7); 1.356(1.9); 1.345(1.9); 1.333 (1.5); 1.284(2.0); 1.255(5.3); 0.997(0.7); 0.978(1.0); 0.880(1.1); 0.008(1.3); 0.000(45.5); 0.009(1.5) Example I-103: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.259(65.1); 7.160(0.6); 7.114(0.5); 7.100(0.6); 7.097(0.8); 7.087(0.7); 7.085(0.6); 4.673(1.6); 4.670(1.6); 4.658(1.6); 4.500(0.7); 2.280(16.0); 1.539(7.5); 0.008(0.8); 0.000(25.8); 0.009 (0.7) Example I-104: .sup.1H-NMR(400.0 MHz, d.sub.6-DMSO): = 8.784(0.9); 7.409(0.5); 7.404(0.9); 7.387(0.9); 7.382(0.6); 7.256 (0.6); 7.249(0.6); 7.232(0.7); 7.229(0.7); 7.226(0.8); 7.223(0.7); 7.206(0.6); 7.199(0.6); 7.086(0.9); 7.083(0.9); 7.079(0.8); 7.077(0.7); 6.107(0.8); 4.412(2.1); 4.398(2.0); 3.324(2.4); 2.519(0.7); 2.510(9.8); 2.506(20.8); 2.501(28.4); 2.496(19.7); 2.492(8.8); 2.125(16.0); 1.988(0.8); 1.175(0.5); 0.000(13.8) Example I-107: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.260(57.0); 7.156(1.0); 7.152(0.7); 7.136(0.9); 7.131(0.9); 7.111(0.7); 4.550(2.3); 4.535(2.4); 4.518(0.9); 2.298(16.0); 1.543(16.9); 0.008(0.7); 0.000(22.9); 0.009(0.7) Example I-109: .sup.1H-NMR(400.6 MHz, CDCl.sub.3): = 7.519(0.9); 7.373(0.6); 7.352(1.3); 7.333(0.9); 7.287(0.7); 7.281(0.8); 7.261(161.6); 7.153(0.7); 7.146(1.0); 7.132(1.2); 7.128(2.7); 7.107(1.1); 7.102(0.8); 6.997(0.9); 4.602(2.1); 4.587(2.0); 4.504(1.0); 2.274(16.0); 1.553(63.5); 0.008(1.9); 0.000(53.9); 0.009(1.7) Example I-11: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.523(0.7); 7.369(0.5); 7.352(1.3); 7.348(0.7); 7.337(0.6); 7.333(1.3); 7.315(0.9); 7.297(0.8); 7.264(110.6); 7.210(1.2); 7.193(0.8); 7.041(2.3); 7.000(0.9); 5.016(2.7); 4.808(2.8); 4.120(1.9); 4.111 (2.0); 4.102(5.4); 4.094(5.6); 4.085(5.5); 4.076(5.7); 4.067(2.2); 4.059(2.1); 3.939(3.6); 3.922(7.7); 3.918(6.2); 3.906 (4.4); 3.901(10.9); 3.885(5.5); 3.828(4.8); 3.811(10.0); 3.807(4.2); 3.794(5.8); 3.790(6.8); 3.781(4.7); 3.772(7.6); 3.766 (4.7); 3.757(4.3); 3.746(5.5); 3.738(5.3); 3.731(5.4); 3.722(5.0); 3.445(5.5); 3.432(5.9); 3.428(5.5); 3.415(5.6); 3.411(5.0); 3.398(4.8); 3.393(4.7); 3.380(4.4); 2.501(1.0); 2.476(8.9); 2.129(0.6); 2.082(1.4); 2.065(3.6); 2.049(4.4); 2.038(2.6); 2.031 (4.5); 2.021(2.2); 2.018(3.9); 2.015(2.6); 2.001(3.6); 1.975(5.4); 1.958(12.0); 1.955(7.3); 1.939(16.0); 1.927(2.5); 1.922 (12.8); 1.904(3.7); 1.665(2.4); 1.647(4.4); 1.635(2.4); 1.629(2.7); 1.626(4.0); 1.615(5.1); 1.608(2.3); 1.597(5.0); 1.578 (1.9); 1.550(0.6); 1.533(0.5); 1.495(0.6); 1.481(0.6); 1.333(1.8); 1.284(2.4); 1.255(2.7); 0.008(1.1); 0.000(42.8); 0.009 (1.4) Example I-111: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.260(51.4); 7.033(0.6); 6.922(0.6); 4.621(1.6); 4.606(1.5); 4.495(0.7); 2.297(3.7); 2.292(3.7); 2.274(16.0); 1.549(8.5); 0.008(0.6); 0.000(20.1); 0.009(0.6) Example I-120: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.375(1.4); 8.370(1.4); 7.695(1.0); 7.688(1.0); 7.674(1.1); 7.668(1.1); 7.339(1.8); 7.319(1.6); 7.261(59.5); 4.590(2.9); 4.575(2.9); 3.964(1.6); 2.287(16.0); 0.008(0.6); 0.000(22.5); 0.009 (0.9) Example I-127: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.519(0.9); 7.310(0.9); 7.260(177.8); 6.996(1.0); 3.267(3.0); 3.251 r(4.4); 3.235(3.1); 2.763(1.5); 2.744(4.8); 2.725(4.9); 2.706(1.6); 1.763(2.6); 1.737(2.8); 1.731(3.0); 1.696(0.9); 1.666(0.8); 1.577(0.9); 1.568(0.9); 1.560(1.0); 1.552(0.8); 1.531(0.6); 1.271(1.3); 1.247(1.2); 1.240(1.5); 1.214(7.9); 1.195(16.0); 1.176 (7.1); 1.151(0.6); 1.019(0.7); 0.990(1.5); 0.965(1.1); 0.882(1.1); 0.008(2.2); 0.006(0.8); 0.000(67.8); 0.009(1.8) Example I-13: .sup.1H-NMR(400.0 MHz, d.sub.6-DMSO): = 9.024(2.3); 9.009(4.4); 8.994(2.3); 8.313(0.8); 7.420(2.2); 7.400(4.9); 7.385(5.1); 7.381(4.0); 7.365(3.1); 7.175(6.5); 7.155(6.0); 7.144(4.6); 7.115(5.8); 7.092(4.7); 7.070(2.4); 7.065(1.9); 6.562(16.0); 4.470(13.6); 4.454(13.6); 3.901(4.3); 3.440(0.4); 3.390(0.6); 3.379(0.7); 3.365(1.3); 3.326(498.5); 3.279(0.9); 3.254(0.4); 3.235(0.4); 2.671(1.8); 2.667(1.4); 2.615(0.4); 2.560(0.5); 2.506(233.8); 2.502(302.1); 2.498(227.5); 2.412 (0.4); 2.333(1.4); 2.329(1.7); 1.400(0.4); 1.299(0.4); 1.258(0.6); 1.231(1.1); 1.155(0.6); 0.000(6.8) Example I-16: .sup.1H-NMR(400.0 MHz, d.sub.6-DMSO): = 9.031(1.9); 9.016(3.6); 9.001(1.9); 8.312(0.7); 7.403(2.6); 7.383(16.0); 7.365(7.4); 7.338(6.2); 7.333(4.3); 7.317(2.7); 7.298(5.6); 7.280(3.6); 6.565(13.0); 4.457(11.1); 4.442(11.0); 3.901 (3.7); 3.448(0.3); 3.440(0.4); 3.432(0.6); 3.412(0.9); 3.397(0.7); 3.393(0.8); 3.389(0.9); 3.374(1.5); 3.361(3.6); 3.331(766.9); 3.293(1.9); 3.287(1.1); 3.280(1.0); 3.271(0.4); 3.267(0.4); 3.261(0.6); 3.243(0.4); 3.164(0.4); 2.676(1.3); 2.672(1.7); 2.667(1.2); 2.570(0.3); 2.564(0.4); 2.560(0.5); 2.555(0.4); 2.511(114.2); 2.507(221.1); 2.502(283.7); 2.498(207.7); 2.494 (102.8); 2.334(1.2); 2.329(1.7); 2.325(1.2); 0.000(3.1) Example I-168: .sup.1H-NMR(400.0 MHz, d.sub.6-DMSO): = 8.271(2.2); 8.257(4.0); 8.242(2.1); 6.051(16.0); 5.845(1.0); 5.830 (2.5); 5.820(1.3); 5.814(1.2); 5.804(3.2); 5.787(3.4); 5.777(1.3); 5.771(1.4); 5.762(2.9); 5.746(1.2); 5.028(4.6); 5.024(5.2); 4.985(4.2); 4.981(4.8); 4.971(5.1); 4.967(4.7); 4.946(4.6); 4.941(4.3); 3.419(9.4); 3.403(9.4); 3.380(0.5); 3.322(507.9); 3.037(7.1); 3.020(11.6); 3.004(7.3); 2.994(1.2); 2.710(0.6); 2.675(1.3); 2.670(1.9); 2.666(1.4); 2.541(146.1); 2.524(4.3); 2.510(104.7); 2.506(214.5); 2.501(286.0); 2.497(214.0); 2.492(108.6); 2.453(0.4); 2.366(0.6); 2.332(1.3); 2.328(1.8); 2.323(1.3); 1.672(8.7); 1.651(9.3); 1.614(2.9); 1.533(0.5); 1.524(0.8); 1.515(1.2); 1.506(1.5); 1.496(1.8); 1.488(2.1); 1.479 (1.8); 1.469(1.6); 1.461(1.3); 1.443(0.6); 1.298(1.1); 1.258(1.5); 1.236(3.2); 1.219(1.1); 1.188(2.7); 1.156(6.1); 1.131 (4.5); 1.100(1.2); 1.071(0.4); 0.925(2.0); 0.898(4.2); 0.871(3.5); 0.843(1.2); 0.837(1.3); 0.000(9.8); 0.008(0.5) Example I-17: .sup.1H-NMR(601.6 MHz, d.sub.6-DMSO): = 9.009(1.9); 8.999(3.8); 8.989(2.0); 7.418(10.4); 7.415(4.0); 7.407 (4.8); 7.404(16.0); 7.400(2.5); 7.350(13.3); 7.336(8.9); 6.568(13.6); 4.433(10.9); 4.423(10.9); 3.904(4.8); 3.326(234.8); 3.172 (0.9); 3.163(0.9); 2.616(1.5); 2.613(2.1); 2.610(1.6); 2.523(3.8); 2.520(4.8); 2.516(5.2); 2.507(117.4); 2.504(241.9); 2.502(327.6); 2.499(247.1); 2.496(122.7); 2.389(1.5); 2.386(2.0); 2.383(1.5); 1.908(0.6); 0.000(5.0) Example I-186: .sup.1H-NMR(400.0 MHz, d.sub.6-DMSO): = 8.855(2.5); 8.841(4.8); 8.826(2.4); 8.313(0.8); 7.400(2.0); 7.379 (4.5); 7.362(4.6); 7.340(2.3); 7.250(2.6); 7.243(2.8); 7.224(3.9); 7.220(4.1); 7.200(2.6); 7.194(2.8); 7.095(2.4); 7.090(2.2); 7.074(4.4); 7.069(4.1); 7.052(2.1); 7.047(1.9); 6.092(16.0); 5.826(1.0); 5.810(2.3); 5.801(1.3); 5.795(1.3); 5.785(3.2); 5.768 (3.4); 5.758(1.4); 5.752(1.5); 5.743(2.7); 5.727(1.2); 4.996(4.6); 4.992(5.3); 4.950(9.6); 4.925(4.9); 4.921(4.4); 4.396 (11.1); 4.382(11.1); 3.901(3.5); 3.430(9.5); 3.414(9.6); 3.389(0.5); 3.373(0.8); 3.364(1.3); 3.355(1.2); 3.322(361.3); 3.275 (0.4); 3.262(0.5); 3.174(0.5); 2.675(1.4); 2.671(1.9); 2.666(1.5); 2.585(0.5); 2.506(245.5); 2.502(318.3); 2.497(239.8); 2.437(0.5); 2.328(1.9); 2.324(1.5); 1.298(1.0); 1.259(1.3); 1.235(0.7); 0.000(8.1) Example I-20: .sup.1H-NMR(400.0 MHz, d.sub.6-DMSO): = 9.037(2.4); 9.022(4.7); 9.007(2.4); 7.561(9.6); 7.541(14.8); 7.468 (15.2); 7.448(9.8); 7.197(0.8); 7.151(5.9); 7.011(12.3); 6.871(5.9); 6.549(16.0); 4.506(10.8); 4.492(10.5); 4.401(0.6); 4.386 (0.5); 3.562(0.5); 3.313(23.8); 3.061(0.8); 3.042(0.7); 2.670(0.8); 2.523(2.5); 2.518(3.8); 2.510(46.2); 2.505(97.8); 2.501 (134.6); 2.496(94.0); 2.491(41.9); 2.332(0.5); 2.327(0.8); 2.323(0.6); 2.278(1.9); 1.254(1.1); 1.236(0.7); 1.191(1.9); 1.173 (3.8); 1.154(1.8); 0.008(1.9); 0.000(56.1); 0.009(1.7) Example I-209: .sup.1H-NMR(400.6 MHz, CDCl.sub.3): = 7.262(15.7); 7.133(0.8); 4.841(0.5); 3.780(16.0); 3.335(4.8); 3.319(7.1); 3.303(4.8); 1.800(1.8); 1.770(3.9); 1.746(1.7); 1.738(2.1); 1.706(1.0); 1.702(1.0); 1.675(1.0); 1.617(0.6); 1.605(0.7); 1.597(0.9); 1.588(1.1); 1.580(0.9); 1.568(0.7); 1.560(0.7); 1.333(0.7); 1.310(0.6); 1.284(1.9); 1.279(1.6); 1.256(3.1); 1.248(2.5); 1.216(1.7); 1.212(1.6); 1.205(0.9); 1.189(0.8); 1.182(1.5); 1.174(0.9); 1.151(1.0); 1.144(0.5); 1.063(0.9); 1.055(0.9); 1.033(1.6); 1.025(2.1); 1.002(1.5); 0.996(1.6); 0.973(0.6); 0.026(0.5); 0.024(0.6); 0.022(0.5); 0.019(0.6); 0.016(0.7); 0.0134(0.8); 0.0125(0.9); 0.012(0.9); 0.008(4.7); 0.000(136.1); 0.006(2.0); 0.009(4.3) Example I-21: .sup.1H-NMR(400.0 MHz, d.sub.6-DMSO): = 9.031(2.4); 9.017(4.6); 9.003(2.3); 7.383(1.5); 7.371(2.2); 7.369(1.6); 7.363(1.7); 7.357(4.1); 7.348(2.0); 7.345(2.1); 7.339(3.9); 7.331(2.2); 7.327(1.8); 7.322(1.3); 7.312(1.8); 7.238(1.5); 7.227(1.0); 7.217(7.8); 7.210(9.3); 7.208(6.7); 7.203(14.0); 7.193(11.4); 7.181(1.1); 7.174(0.9); 6.553(16.0); 4.531(13.3); 4.517(13.1); 3.310(50.0); 2.670(0.5); 2.524(1.6); 2.519(2.4); 2.510(29.2); 2.506(62.1); 2.501(85.9); 2.497(60.0); 2.492 (26.9); 2.328(0.5); 1.988(0.5); 0.008(1.3); 0.000(40.3); 0.009(1.2) Example I-227: 1H-NMR(400.6 MHz, CDCl.sub.3): = 7.519(1.1); 7.508(1.0); 7.436(1.0); 7.415(2.3); 7.399(2.4); 7.394(1.5); 7.378(1.3); 7.260(54.4); 6.896(1.1); 6.893(1.0); 6.890(1.4); 6.887(1.4); 6.875(1.7); 6.867(5.0); 6.862(1.0); 6.854(1.0); 6.846(3.3); 6.836(1.5); 6.820(1.9); 6.814(1.3); 4.834(2.5); 4.652(6.6); 4.637(6.4); 3.760(16.0); 1.551(2.7); 1.256(0.8); 0.146(1.5); 0.100(0.9); 0.039(0.9); 0.028(1.3); 0.026(1.5); 0.022(1.8); 0.019(1.6); 0.013(2.9); 0.008(15.7); 0.000(465.9); 0.009(13.2); 0.012(1.0); 0.014(0.6); 0.018(0.8); 0.050(0.5); 0.149(1.5) Example I-23: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.520(1.4); 7.273(0.8); 7.270(1.4); 7.268(2.1); 7.261(249.4); 7.254(1.2); 7.253(0.8); 7.2523(0.8); 7.2516(0.6); 7.145(2.8); 7.138(3.2); 7.131(3.1); 7.124(5.4); 7.117(3.5); 7.110(3.1); 7.102(3.3); 7.077(4.4); 7.066(4.9); 7.054(8.9); 7.043(8.3); 7.032(5.6); 7.021(5.3); 7.008(3.0); 7.000(3.0); 6.997(4.0); 6.990(4.8); 6.985 (2.0); 6.981(3.1); 6.979(4.2); 6.971(2.7); 6.967(2.5); 6.956(1.6); 6.948(1.3); 4.749(7.1); 4.680(16.0); 4.665(15.7); 1.555 (24.9); 1.333(1.8); 1.284(2.5); 1.255(2.3); 0.008(3.1); 0.000(115.2); 0.009(3.4); 0.011(0.6) Example I-24: .sup.1H-NMR(400.0 MHz, d.sub.6-DMSO): = 8.907(2.5); 8.893(4.5); 8.880(2.4); 7.446(1.8); 7.429(3.7); 7.424(3.1); 7.412(2.3); 7.408(7.2); 7.404(2.6); 7.391(3.2); 7.387(4.5); 7.370(2.0); 7.134(1.0); 7.130(1.5); 7.119(9.3); 7.109(1.7); 7.099(15.4); 7.089(1.8); 7.079(8.2); 7.067(1.3); 7.064(0.9); 6.511(16.0); 4.500(13.3); 4.487(13.2); 3.868(1.2); 3.311(30.8); 3.170(2.6); 2.670(0.6); 2.524(1.7); 2.519(2.5); 2.510(36.6); 2.506(80.1); 2.501(111.9); 2.496(78.2); 2.492(35.3); 2.456 (0.9); 2.452(0.9); 2.328(0.6); 0.008(1.1); 0.000(38.1); 0.009(1.1) Example I-25: .sup.1H-NMR(400.0 MHz, d.sub.6-DMSO): = 9.003(2.4); 8.988(4.4); 8.973(2.3); 7.443(3.7); 7.422(8.0); 7.416(3.9); 7.401(4.8); 7.395(9.3); 7.388(3.3); 7.374(7.2); 7.368(3.5); 7.364(3.3); 7.358(3.1); 7.344(2.9); 7.339(3.0); 7.194(2.3); 7.191(3.0); 7.189(3.0); 7.186(2.9); 7.184(3.0); 7.180(3.1); 7.178(3.0); 7.175(3.1); 7.170(2.7); 7.168(2.6); 7.164(2.4); 7.162 (2.4); 7.159(2.4); 6.550(16.0); 4.436(13.7); 4.421(13.5); 3.358(0.7); 3.343(0.6); 3.309(132.6); 2.675(0.8); 2.670(1.1); 2.665(0.8); 2.550(0.7); 2.545(0.8); 2.540(0.9); 2.536(0.8); 2.523(3.3); 2.519(5.0); 2.510(63.8); 2.505(136.8); 2.501(190.6); 2.496(132.5); 2.492(58.8); 2.332(0.8); 2.328(1.2); 2.323(0.8); 1.256(0.5); 1.183(0.8); 1.164(1.5); 1.146(0.7); 0.008(2.1); 0.000(66.9); 0.009(1.9) Example I-250: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.518(8.9); 7.351(1.3); 7.323(1.1); 7.292(2.0); 7.270(9.2); 7.269(9.9); 7.259(1578.2); 7.255(11.3); 7.254(8.0); 7.253(6.3); 7.252(4.9); 7.251(3.8); 7.2504(3.5); 7.2496(2.9); 7.249(2.1); 7.248 (1.9); 7.247(1.5); 7.2464(1.6); 7.2456(1.4); 7.245(1.4); 7.244(1.2); 7.243(1.5); 7.242(1.5); 7.209(2.7); 6.995(8.3); 5.970 (1.5); 4.863(5.3); 3.296(11.2); 3.280(16.0); 3.264(10.9); 1.758(8.0); 1.734(9.3); 1.699(2.7); 1.669(2.2); 1.566(3.7); 1.538 (68.4); 1.422(4.6); 1.404(2.6); 1.333(4.0); 1.307(6.0); 1.284(7.3); 1.281(5.6); 1.274(4.0); 1.256(6.3); 1.243(5.2); 1.208(4.3); 1.182(3.1); 1.152(2.2); 1.121(0.9); 1.022(2.1); 0.995(4.4); 0.971(3.8); 0.933(1.3); 0.880(1.1); 0.157(1.8); 0.146(1.7); 0.008 (17.8); 0.000(612.6); 0.009(16.9); 0.051(1.0); 0.150(1.9) Example I-254: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.519(3.9); 7.323(0.5); 7.286(0.7); 7.276(1.4); 7.270(2.7); 7.260(701.7); 7.230(0.8); 7.211(0.9); 6.996(3.9); 6.463(5.0); 4.881(8.7); 3.987(8.6); 3.969(4.9); 3.964(8.2); 3.960(10.5); 3.954(7.8); 3.742(9.4); 3.734(10.0); 3.724(9.5); 3.717(10.0); 3.708(10.9); 3.700(11.5); 3.690(10.7); 3.682(11.2); 3.488(4.3); 3.481 (5.3); 3.475(4.3); 3.468(9.7); 3.461(12.9); 3.455(15.3); 3.447(6.8); 3.440(11.3); 3.431(16.0); 3.412(5.8); 3.403(7.2); 3.228 (11.8); 3.218(11.9); 3.208(10.1); 3.197(10.9); 3.194(11.4); 3.183(10.3); 3.174(9.2); 3.163(8.9); 1.884(7.1); 1.873(6.1); 1.863(6.1); 1.854(5.4); 1.844(3.6); 1.627(9.5); 1.616(5.7); 1.595(13.2); 1.591(12.1); 1.585(9.5); 1.577(4.6); 1.562(10.3); 1.552(15.2); 1.548(14.1); 1.543(20.4); 1.537(26.5); 1.533(24.0); 1.528(24.5); 1.508(6.3); 1.498(7.2); 1.488(3.4); 1.477 (2.1); 1.467(2.8); 1.457(2.0); 1.402(1.2); 1.380(4.7); 1.369(2.4); 1.349(8.3); 1.339(5.6); 1.333(4.3); 1.321(7.6); 1.310(4.8); 1.290(4.4); 1.284(4.6); 1.256(9.0); 0.897(0.8); 0.880(2.0); 0.863(0.9); 0.331(1.2); 0.238(0.9); 0.156(1.2); 0.146(0.9); 0.069 (3.4); 0.008(7.4); 0.000(271.2); 0.009(8.0); 0.150(0.9) Example I-258: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.519(1.6); 7.406(2.6); 7.402(2.9); 7.387(5.5); 7.383(6.1); 7.368(3.0); 7.364(3.5); 7.343(1.9); 7.339(1.9); 7.330(2.1); 7.324(4.2); 7.320(3.0); 7.311(3.1); 7.309(2.8); 7.304(4.6); 7.299(2.7); 7.290 (2.9); 7.286(2.6); 7.260(295.3); 7.250(0.6); 7.210(0.8); 7.167(5.4); 7.164(6.2); 7.148(8.9); 7.145(9.8); 7.129(3.9); 7.126 (4.1); 7.109(4.7); 7.106(4.4); 7.088(4.1); 7.084(5.7); 7.080(4.6); 7.062(3.8); 7.060(3.7); 6.996(1.6); 6.331(1.8); 4.868 (4.5); 4.664(16.0); 4.649(15.7); 1.621(1.2); 1.332(0.8); 1.284(1.3); 1.256(5.3); 0.880(1.0); 0.008(3.2); 0.006(1.1); 0.0054 (1.2); 0.0046(1.5); 0.000(108.0); 0.006(1.2); 0.007(0.9); 0.009(3.2) Example I-26: .sup.1H-NMR(299.9 MHz, d.sub.6-DMSO): = 9.048(2.3); 9.028(4.5); 9.009(2.4); 7.169(1.0); 7.161(2.1); 7.154(1.4); 7.138(2.0); 7.130(4.0); 7.122(2.8); 7.107(1.1); 7.099(2.1); 7.091(1.6); 7.069(1.4); 7.048(7.0); 7.026(7.1); 6.572(16.0); 5.755(0.6); 4.476(12.7); 4.456(12.8); 3.314(113.9); 2.733(0.6); 2.726(0.7); 2.512(31.4); 2.506(63.2); 2.501(87.0); 2.495 (67.1); 2.271(0.7); 1.231(1.6); 1.139(0.4); 0.010(1.6); 0.000(31.7) Example I-268: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.518(10.6); 7.414(3.1); 7.393(6.4); 7.377(6.3); 7.372(3.8); 7.356(4.0); 7.293(3.3); 7.259(1935.6); 7.252(5.5); 7.251(4.2); 7.2503(3.3); 7.2495(3.1); 7.249(2.8); 7.247(1.8); 7.246(1.2); 7.244 (1.4); 7.227(1.6); 7.209(1.3); 6.995(10.4); 6.910(2.7); 6.907(2.7); 6.904(3.7); 6.889(4.5); 6.881(6.8); 6.872(5.6); 6.866(4.8); 6.860(4.0); 6.850(5.3); 6.847(5.4); 6.841(4.2); 6.825(5.0); 6.819(3.9); 6.305(2.4); 4.869(7.2); 4.616(16.0); 4.601(15.8); 1.536(85.4); 1.422(6.1); 1.404(2.6); 1.333(5.9); 1.307(5.1); 1.284(8.5); 1.281(4.5); 1.256(7.7); 1.232(1.8); 0.880(1.6); 0.157 (2.2); 0.146(2.4); 0.008(22.1); 0.006(8.3); 0.000(734.2); 0.009(19.1); 0.150(2.0) Example I-27: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.519(1.8); 7.387(5.3); 7.376(1.7); 7.373(1.2); 7.366(10.6); 7.346(6.2); 7.260(319.9); 7.254(2.4); 7.253(1.8); 7.2524(1.4); 7.2516(1.2); 7.251(1.0); 7.250(0.8); 7.249(0.6); 7.248(0.6); 7.154(5.5); 7.148(8.8); 7.142(9.3); 7.137(9.1); 7.131(7.8); 7.126(3.0); 7.117(9.2); 7.112(6.1); 7.034(2.1); 6.996(2.0); 4.738(2.3); 4.665 (16.0); 4.649(15.6); 2.043(1.0); 1.552(1.8); 1.258(0.7); 0.008(3.7); 0.000(127.3); 0.009(3.8) Example I-28: .sup.1H-NMR(400.6 MHz, DMSO): = 8.955(1.4); 8.941(2.5); 8.927(1.2); 7.277(1.0); 7.256(2.2); 7.231(2.2); 7.209(1.4); 7.136(1.7); 7.126(2.0); 7.105(1.2); 6.559(9.3); 4.459(0.7); 4.444(0.8); 4.424(6.4); 4.409(6.3); 3.332(15.5); 2.675(0.9); 2.670(1.3); 2.666(1.0); 2.524(6.0); 2.519(8.2); 2.511(70.2); 2.506(144.8); 2.501(198.9); 2.497(137.7); 2.492(61.0); 2.333(0.9); 2.329(1.3); 2.324(1.1); 2.271(16.0); 2.266(15.9); 2.219(1.3); 2.214(1.3); 1.989(0.7); 0.008(4.9); 0.000(160.1); 0.007(1.7); 0.009(4.8); 0.013(0.6) Example I-29: .sup.1H-NMR(400.0 MHz, d.sub.6-DMSO): = 8.989(1.1); 8.974(2.1); 8.960(1.1); 7.106(0.8); 7.088(9.8); 7.076(9.6); 7.056(0.8); 6.543(7.5); 4.479(5.9); 4.465(5.9); 3.308(32.8); 2.523(0.9); 2.519(1.4); 2.510(17.9); 2.506(38.1); 2.501(52.8); 2.496(36.9); 2.492(16.5); 2.263(16.0); 2.257(16.0); 1.175(0.6); 1.172(0.6); 0.008(0.8); 0.000(24.2); 0.009(0.7) Example I-291: .sup.1H-NMR(400.0 MHz, d.sub.6-DMSO): = 8.313(0.7); 7.826(2.4); 7.811(4.2); 7.798(2.3); 7.465(4.3); 7.448 (12.5); 7.429(12.7); 7.410(6.6); 7.406(4.9); 7.399(2.1); 7.392(7.1); 7.385(1.5); 7.374(2.2); 7.360(12.7); 7.356(15.2); 7.340 (10.9); 5.827(16.0); 3.901(3.9); 3.431(0.3); 3.426(0.3); 3.382(0.5); 3.374(0.6); 3.368(0.8); 3.322(407.8); 3.282(1.0); 3.265 (0.5); 3.252(0.5); 3.237(0.4); 3.230(0.3); 2.898(8.0); 2.882(14.1); 2.867(8.1); 2.670(2.1); 2.666(1.5); 2.607(0.3); 2.506 (271.6); 2.501(351.0); 2.497(264.2); 2.452(0.9); 2.443(0.6); 2.433(0.6); 2.418(0.6); 2.333(1.5); 2.328(2.1); 1.558(8.2); 1.549 (8.9); 1.375(5.3); 1.342(5.7); 1.298(0.6); 1.259(1.4); 1.251(1.3); 1.235(2.9); 1.224(2.4); 1.215(2.7); 1.207(2.2); 1.197 (1.9); 1.187(1.6); 1.179(1.0); 1.160(0.4); 1.116(0.8); 1.112(0.9); 1.081(3.0); 1.052(9.6); 1.032(6.1); 1.010(1.4); 0.978(0.4); 0.854(0.4); 0.707(1.9); 0.678(4.6); 0.648(3.8); 0.625(1.3); 0.618(1.2); 0.000(9.3) Example I-30: .sup.1H-NMR(400.0 MHz, d.sub.6-DMSO): = 8.931(0.9); 8.917(1.6); 8.902(0.9); 7.270(1.3); 7.251(2.7); 7.230(1.4); 7.031(2.0); 7.007(3.4); 6.991(2.0); 6.546(5.8); 4.439(4.2); 4.424(4.2); 3.901(1.5); 3.365(0.6); 3.325(203.0); 3.279(0.4); 2.671(0.7); 2.667(0.5); 2.506(86.3); 2.502(110.6); 2.498(83.7); 2.455(0.4); 2.328(0.7); 2.324(0.6); 2.297(16.0); 0.000 (2.4) Example I-31: .sup.1H-NMR(400.0 MHz, d.sub.6-DMSO): = 8.953(0.8); 8.939(1.5); 8.926(0.8); 7.231(1.4); 7.215(1.6); 7.210(1.8); 7.195(1.6); 7.059(1.5); 7.052(2.0); 7.033(1.6); 7.026(2.2); 7.016(1.0); 7.001(2.4); 6.994(1.6); 6.980(1.1); 6.973(0.8); 6.554(5.1); 4.419(5.4); 4.404(5.3); 3.336(5.4); 3.170(1.5); 2.523(0.8); 2.518(1.2); 2.510(15.4); 2.505(32.9); 2.501(45.4); 2.496(31.5); 2.491(14.0); 2.278(16.0); 0.008(0.6); 0.000(18.4); 0.009(0.5) Example I-32: .sup.1H-NMR(400.0 MHz, d.sub.6-DMSO): = 8.909(2.4); 8.896(4.5); 8.884(2.3); 7.233(0.7); 7.224(1.4); 7.215(7.9); 7.193(10.4); 7.171(7.6); 7.162(1.3); 7.153(0.5); 6.516(16.0); 4.448(12.0); 4.435(11.9); 4.039(0.7); 4.021(0.6); 3.360 (0.8); 3.308(116.3); 2.674(0.8); 2.670(1.1); 2.665(0.8); 2.556(0.6); 2.551(0.7); 2.546(0.5); 2.523(2.7); 2.519(4.2); 2.510(58.9); 2.505(127.7); 2.501(178.9); 2.496(124.6); 2.491(55.5); 2.475(0.8); 2.470(0.7); 2.332(0.8); 2.328(1.1); 2.323(0.8); 1.988 (3.1); 1.255(0.7); 1.193(1.1); 1.175(2.3); 1.157(1.5); 0.008(2.8); 0.000(95.7); 0.006(0.9); 0.007(0.8); 0.009(2.7) Example I-33: .sup.1H-NMR(400.0 MHz, d.sub.6-DMSO): = 9.041(2.5); 9.026(4.6); 9.011(2.3); 7.499(1.6); 7.491(1.6); 7.483(1.6); 7.477(2.4); 7.471(2.4); 7.463(2.4); 7.450(2.4); 7.443(1.5); 7.435(1.4); 7.427(1.3); 7.092(1.7); 7.084(2.3); 7.079(2.9); 7.069(2.7); 7.057(3.0); 6.563(16.0); 4.527(11.8); 4.512(11.6); 4.057(0.7); 4.039(1.9); 4.021(2.0); 4.003(0.6); 3.309(149.8); 2.674(1.1); 2.670(1.6); 2.665(1.1); 2.523(4.4); 2.519(6.5); 2.510(95.3); 2.505(207.8); 2.501(290.5); 2.496(200.0); 2.492 (88.5); 2.332(1.2); 2.328(1.5); 2.323(1.1); 1.988(9.3); 1.193(2.9); 1.175(6.2); 1.157(3.3); 0.008(4.1); 0.000(151.4); 0.009 (4.4) Example I-332: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.260(40.0); 4.919(0.7); 3.360(1.3); 3.344(1.8); 3.328(1.3); 2.334(16.0); 1.780(1.0); 1.549(4.0); 1.286(0.9); 1.285(0.8); 1.258(1.0); 0.000(15.4) Example I-34: .sup.1H-NMR(400.0 MHz, d.sub.6-DMSO): = 8.974(2.5); 8.961(4.7); 8.948(2.4); 7.510(1.5); 7.497(1.6); 7.487(3.2); 7.474(3.2); 7.462(3.2); 7.449(3.1); 7.439(1.6); 7.426(1.4); 7.175(1.8); 7.169(2.0); 7.165(1.9); 7.160(1.9); 7.152(3.2); 7.146(3.6); 7.142(3.3); 7.137(3.2); 7.129(1.6); 7.123(1.7); 7.119(1.5); 7.114(1.4); 6.521(16.0); 4.524(11.5); 4.511(11.3); 3.314(26.5); 3.170(4.2); 2.671(0.6); 2.524(1.8); 2.519(2.6); 2.511(36.0); 2.506(77.9); 2.501(108.4); 2.497(74.7); 2.492 (33.3); 2.328(0.6); 1.187(0.8); 1.169(1.5); 1.151(0.8); 0.008(1.4); 0.000(45.6); 0.009(1.3) Example I-35: .sup.1H-NMR(400.0 MHz, d.sub.6-DMSO): = 9.024(2.3); 9.009(4.4); 8.994(2.2); 8.313(1.0); 7.301(0.7); 7.293(1.1); 7.284(6.8); 7.267(7.2); 7.262(7.3); 7.245(6.7); 7.235(1.1); 7.229(0.7); 6.572(16.0); 4.439(11.6); 4.424(11.5); 3.901(5.6); 3.396(0.4); 3.385(0.4); 3.377(0.4); 3.361(1.0); 3.354(1.0); 3.351(1.1); 3.322(452.2); 3.302(3.0); 3.278(0.7); 3.272(0.6); 3.255(0.4); 3.104(0.4); 3.086(0.4); 2.675(1.6); 2.671(2.2); 2.667(1.8); 2.610(0.4); 2.535(1.1); 2.524(5.7); 2.511(141.3); 2.506(280.6); 2.502(367.8); 2.497(273.6); 2.493(139.1); 2.452(0.8); 2.422(0.4); 2.333(1.6); 2.329(2.2); 2.324(1.7); 1.250 (0.4); 1.236(0.4); 1.195(0.8); 1.177(1.8); 1.159(1.0); 0.008(0.4); 0.000(9.9) Example I-350: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.426(0.5); 7.410(0.5); 7.260(51.9); 6.869(1.3); 6.849(0.9); 4.920(0.8); 4.672(1.5); 4.657(1.5); 2.2 82(16.0); 1.543(10.2); 1.286(0.5); 0.008(0.6); 0.000(19.9); 0.009(0.5) Example I-36: .sup.1H-NMR(400.0 MHz, d.sub.6-DMSO): = 9.022(2.4); 9.008(4.5); 8.993(2.3); 7.357(1.4); 7.352(1.4); 7.339(1.6); 7.335(3.3); 7.330(2.9); 7.317(2.5); 7.312(3.5); 7.310(3.6); 7.305(2.3); 7.291(2.1); 7.287(2.3); 7.269(1.8); 7.263(1.9); 7.249(3.6); 7.235(2.1); 7.229(2.8); 7.213(0.9); 7.207(1.0); 6.552(16.0); 4.494(11.4); 4.480(11.2); 4.039(0.5); 4.021(0.5); 3.308(108.7); 2.675(0.8); 2.670(1.1); 2.665(0.8); 2.523(3.8); 2.519(5.7); 2.510(61.5); 2.505(127.0); 2.501(173.3); 2.496 (121.1); 2.492(54.3); 2.332(0.7); 2.328(1.0); 2.323(0.7); 1.988(2.3); 1.256(0.7); 1.193(0.8); 1.175(1.5); 1.157(0.9); 0.008 (2.1); 0.000(60.4); 0.009(1.9) Example I-37: .sup.1H-NMR(400.0 MHz, d.sub.6-DMSO): = 9.049(2.7); 9.035(5.2); 9.020(2.6); 8.352(6.5); 8.347(6.9); 8.340(6.7); 8.335(6.6); 7.818(5.9); 7.816(4.6); 7.814(6.0); 7.799(6.6); 7.795(6.4); 7.476(8.3); 7.464(8.1); 7.457(7.5); 7.445(7.2); 6.583(16.0); 4.514(14.8); 4.499(14.5); 3.374(0.6); 3.357(0.7); 3.323(136.6); 2.671(0.6); 2.524(3.4); 2.511(34.8); 2.507 (70.1); 2.502(94.9); 2.497(67.1); 2.493(30.4); 2.329(0.6); 2.086(1.8); 1.259(0.6); 1.235(1.2); 0.008(0.7); 0.000(16.7) Example I-373: .sup.1H-NMR(400.6 MHz, CDCl.sub.3): = 8.216(0.6); 7.268(3.4); 5.018(1.7); 4.011(0.9); 3.899(0.5); 3.351(3.3); 3.335(4.9); 3.319(3.3); 2.823(2.1); 2.805(6.8); 2.787(6.8); 2.768(2.2); 1.820(1.2); 1.815(1.4); 1.782(2.9); 1.764(0.9); 1.761(0.9); 1.754(1.2); 1.746(1.5); 1.711(0.7); 1.707(0.8); 1.703(0.6); 1.699(0.5); 1.679(0.7); 1.624(0.5); 1.616(0.6); 1.607(0.7); 1.599(0.6); 1.285(1.6); 1.266(8.2); 1.255(4.0); 1.248(16.0); 1.229(7.6); 1.220(1.3); 1.212(0.7); 1.197(0.6); 1.189(1.1); 1.182(0.6); 1.159(0.6); 1.086(0.7); 1.080(0.7); 1.049(1.5); 1.020(1.3); 0.000(5.4) Example I-38: .sup.1H-NMR(400.0 MHz, d.sub.6-DMSO): = 9.038(2.4); 9.024(4.6); 9.009(2.3); 8.435(0.6); 8.383(9.7); 8.381(10.1); 8.376(10.1); 8.375(9.6); 8.285(0.6); 7.817(7.2); 7.810(7.0); 7.796(8.2); 7.790(7.8); 7.703(0.6); 7.570(0.6); 7.549(0.6); 7.523(13.1); 7.521(12.8); 7.502(11.2); 7.501(11.0); 7.474(0.8); 7.453(0.7); 6.554(16.0); 4.473(16.0); 4.458(15.8); 4.230 (1.0); 4.215(0.9); 4.039(1.4); 4.021(1.4); 4.003(0.6); 3.963(1.5); 3.309(121.9); 2.675(1.1); 2.670(1.4); 2.665(1.0); 2.523 (4.2); 2.519(6.3); 2.510(89.2); 2.505(194.3); 2.501(271.0); 2.496(186.6); 2.492(82.5); 2.332(0.9); 2.328(1.5); 2.323(1.0); 2.072(0.9); 1.988(6.6); 1.247(0.6); 1.193(1.9); 1.175(3.7); 1.157(1.9); 0.008(2.8); 0.000(97.1); 0.009(2.8) Example I-39: .sup.1H-NMR(400.0 MHz, d.sub.6-DMSO): = 9.066(2.4); 9.052(4.6); 9.037(2.4); 8.496(10.2); 8.489(10.2); 8.443 (10.0); 7.668(3.2); 7.664(3.9); 7.662(3.9); 7.657(3.0); 7.644(3.1); 7.639(3.9); 7.637(3.8); 7.633(3.0); 6.571(16.0); 4.526 (14.5); 4.511(14.4); 3.325(174.9); 2.672(0.5); 2.525(1.7); 2.520(2.5); 2.512(29.6); 2.507(61.7); 2.503(84.2); 2.498(58.8); 2.493(26.2); 2.086(1.3); 0.000(13.6) Example I-391: .sup.1H-NMR(400.6 MHz, CDCl.sub.3): = 8.603(0.7); 7.447(0.5); 7.426(1.3); 7.410(1.4); 7.405(1.0); 7.389(0.8); 7.265(5.6); 6.896(0.7); 6.894(0.6); 6.890(0.9); 6.887(0.9); 6.875(1.2); 6.873(1.1); 6.868(3.6); 6.855(0.7); 6.847(3.0); 6.839(1.0); 6.823(1.1); 6.817(0.8); 4.959(2.7); 4.660(4.1); 4.646(4.0); 2.755(2.3); 2.737(7.3); 2.719(7.4); 2.700(2.4); 1.663(1.7); 1.334(0.6); 1.285(0.9); 1.256(1.8); 1.176(7.8); 1.158(16.0); 1.139(7.4); 0.000(6.6) Example I-40: .sup.1H-NMR(400.0 MHz, d.sub.6-DMSO): = 9.099(2.4); 9.084(4.5); 9.069(2.2); 8.216(9.4); 8.203(9.5); 7.306(3.5); 7.303(4.7); 7.301(4.8); 7.297(3.9); 7.293(3.7); 7.290(4.5); 7.288(4.4); 7.285(3.3); 7.081(9.5); 6.591(16.0); 4.543(13.2); 4.528(12.8); 3.329(64.6); 2.527(1.6); 2.522(2.1); 2.513(12.9); 2.509(26.3); 2.504(35.8); 2.500(25.3); 2.495(11.6); 2.087 (0.7); 1.990(1.3); 1.176(0.8); 0.000(7.8) Example I-41: .sup.1H-NMR(400.0 MHz, d.sub.6-DMSO): = 8.667(0.6); 8.653(1.1); 8.640(0.6); 7.528(4.2); 6.517(4.0); 4.215(3.8); 4.201(3.8); 4.019(1.3); 4.001(4.0); 3.983(4.1); 3.965(1.3); 3.323(114.1); 3.303(0.5); 2.675(0.3); 2.670(0.5); 2.666(0.3); 2.541(3.6); 2.524(1.1); 2.510(29.7); 2.506(58.6); 2.501(75.6); 2.497(55.2); 2.492(27.1); 2.332(0.4); 2.328(0.5); 2.324 (0.4); 2.128(16.0); 1.321(4.7); 1.303(10.1); 1.285(4.6); 1.236(0.4); 0.000(2.4) Example I-414: .sup.1H-NMR(400.0 MHz, d.sub.6-DMSO): = 8.425(2.2); 8.411(4.2); 8.396(2.2); 8.312(0.8); 7.328(5.3); 7.309 (13.2); 7.290(9.8); 7.221(4.7); 7.203(6.9); 7.185(2.4); 7.133(13.6); 7.115(11.2); 6.324(16.0); 3.901(4.5); 3.426(0.3); 3.399 (0.6); 3.376(1.3); 3.351(2.8); 3.326(603.6); 3.284(1.7); 3.257(0.8); 3.247(0.5); 3.239(0.5); 3.218(0.3); 3.175(0.6); 3.163 (0.4); 3.094(7.2); 3.078(13.1); 3.063(7.4); 2.675(1.5); 2.671(2.0); 2.553(0.7); 2.506(257.3); 2.502(335.4); 2.498(255.2); 2.438(0.5); 2.433(0.5); 2.423(0.5); 2.328(2.0); 2.324(1.5); 1.584(9.2); 1.561(13.6); 1.459(1.8); 1.414(1.5); 1.397(2.1); 1.389 (1.8); 1.368(1.4); 1.335(0.7); 1.298(1.5); 1.259(2.0); 1.249(0.7); 1.235(0.6); 1.133(1.0); 1.103(2.7); 1.073(4.8); 1.051 (5.2); 1.003(1.3); 0.974(0.5); 0.865(2.2); 0.838(4.5); 0.811(3.6); 0.777(1.2); 0.000(7.3) Example I-432: .sup.1H-NMR(400.0 MHz, d.sub.6-DMSO): = 9.043(2.4); 9.028(4.7); 9.014(2.4); 8.313(0.9); 7.325(2.4); 7.316 (5.6); 7.311(3.5); 7.298(14.4); 7.287(5.5); 7.279(11.5); 7.266(2.5); 7.230(5.4); 7.227(3.8); 7.219(3.7); 7.212(9.6); 7.193(6.0); 7.190(4.8); 7.170(2.7); 7.163(2.8); 7.135(10.9); 7.132(14.4); 7.114(11.1); 6.964(2.2); 6.960(2.1); 6.945(3.9); 6.943(4.1); 6.939(3.9); 6.921(2.0); 6.917(1.9); 6.344(16.0); 4.456(10.7); 4.441(10.7); 3.901(4.9); 3.471(0.4); 3.456(0.5); 3.432(0.4); 3.414(0.3); 3.381(0.4); 3.371(1.4); 3.354(3.4); 3.324(599.9); 3.286(0.9); 3.270(0.9); 3.264(0.7); 3.255(0.7); 3.245(0.4); 2.675(1.7); 2.671(2.2); 2.666(1.7); 2.627(0.3); 2.610(0.3); 2.598(0.4); 2.590(0.4); 2.524(7.2); 2.510(146.7); 2.506(286.5); 2.502(372.2); 2.497(273.9); 2.493(137.1); 2.452(0.6); 2.447(0.8); 2.333(1.6); 2.328(2.2); 2.324(1.6); 1.422(0.4); 1.336 (0.4); 1.298(1.4); 1.259(1.9); 1.250(0.5); 1.235(0.6); 0.000(9.5) Example I-44: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.525(2.2); 7.301(0.6); 7.267(398.6); 7.259(1.1); 7.217(0.6); 7.002(2.2); 6.536(1.7); 4.845(6.1); 3.438(14.4); 3.423(15.4); 3.420(16.0); 3.405(14.5); 2.583(0.8); 2.578(1.1); 2.573(0.8); 2.219 (1.8); 2.200(4.6); 2.181(6.4); 2.162(5.0); 2.143(2.2); 1.886(1.7); 1.869(3.4); 1.867(3.3); 1.857(4.9); 1.851(3.5); 1.842(4.2); 1.838(5.6); 1.829(3.2); 1.826(3.6); 1.814(1.8); 1.809(2.3); 1.698(7.2); 1.690(6.0); 1.686(5.7); 1.677(6.6); 1.665(5.0); 1.660 (5.9); 1.654(4.1); 1.644(3.6); 1.638(3.3); 1.635(4.8); 1.631(3.3); 1.623(2.6); 1.616(5.5); 1.615(5.3); 1.612(4.9); 1.605 (4.5); 1.595(5.8); 1.590(4.3); 1.586(3.7); 1.583(3.8); 1.576(3.5); 1.573(3.1); 1.565(1.8); 1.551(0.9); 1.546(0.7); 1.454(0.8); 1.432(0.9); 1.422(0.6); 1.333(3.3); 1.322(2.0); 1.316(4.5); 1.309(2.6); 1.302(4.3); 1.297(5.2); 1.285(6.3); 1.267(4.5); 1.256 (6.0); 0.880(0.8); 0.853(0.5); 0.008(4.4); 0.000(143.6); 0.009(3.8) Example I-455: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.519(1.8); 7.260(346.4); 7.253(1.1); 7.252(1.0); 7.210(0.6); 6.996 (1.9); 6.874(6.4); 6.845(6.9); 6.829(7.2); 6.800(7.4); 6.018(1.4); 5.738(11.1); 5.735(12.9); 5.693(11.9); 5.690(16.0); 5.688 (9.4); 5.662(8.8); 5.659(7.8); 4.639(5.4); 3.271(10.1); 3.255(14.7); 3.239(10.0); 1.771(2.8); 1.750(7.8); 1.727(9.2); 1.701 (2.6); 1.695(2.6); 1.665(2.1); 1.595(0.7); 1.586(1.1); 1.566(2.4); 1.550(11.5); 1.521(1.5); 1.512(1.0); 1.422(0.9); 1.370 (0.5); 1.333(8.8); 1.305(1.2); 1.298(1.6); 1.284(13.1); 1.257(10.0); 1.242(3.3); 1.236(4.8); 1.212(3.3); 1.202(4.6); 1.183(1.6); 1.177(3.1); 1.169(1.9); 1.154(1.0); 1.146(2.2); 1.139(1.2); 1.115(0.8); 1.014(2.2); 0.986(4.1); 0.962(3.6); 0.955(3.1); 0.933(1.2); 0.925(1.3); 0.897(0.8); 0.880(2.3); 0.863(1.0); 0.012(0.5); 0.008(4.1); 0.006(1.4); 0.0054(1.6); 0.0046(2.0); 0.000 (132.7); 0.006(1.4); 0.007(1.1); 0.009(3.9) Example I-46: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.519(2.0);7.295(0.7); 7.260(384.0); 6.996(2.1); 6.507(1.6); 4.833(2.3); 3.356(9.4); 3.341(16.0); 3.325(9.1); 1.852(0.7); 1.828(4.1); 1.819(5.2); 1.809(7.6); 1.802(5.4); 1.794(5.9); 1.784(5.7); 1.777(4.8); 1.767(3.3); 1.757(1.4); 1.736(2.8); 1.729(3.2); 1.719(4.4); 1.712(4.6); 1.703(4.1); 1.695(4.5); 1.686(3.9); 1.679 (3.9); 1.647(1.4); 1.639(1.7); 1.628(2.2); 1.619(3.1); 1.611(3.3); 1.607(2.9); 1.601(3.2); 1.594(5.0); 1.583(4.4); 1.571 (2.4); 1.552(4.6); 1.544(3.2); 1.529(5.1); 1.521(4.2); 1.514(3.0); 1.502(7.2); 1.497(6.8); 1.489(4.3); 1.477(6.0); 1.454(3.3); 1.449(3.5); 1.434(1.5); 1.426(1.9); 1.337(2.6); 1.333(2.4); 1.312(4.3); 1.302(4.9); 1.294(3.2); 1.287(3.9); 1.284(3.9); 1.277 (4.5); 1.269(3.4); 1.255(7.6); 0.880(1.0); 0.008(3.9); 0.000(148.2); 0.009(4.4) Example I-473: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.525(0.6); 7.518(2.6); 7.413(2.2); 7.396(2.7); 7.391(4.7); 7.375(4.9); 7.370(2.9); 7.354(3.0); 7.350(1.1); 7.310(0.5); 7.294(0.8); 7.260(492.3); 6.996(2.6); 6.894(2.3); 6.892(2.1); 6.888(2.8); 6.886(3.0); 6.874(3.6); 6.872(3.5); 6.865(6.4); 6.860(4.5); 6.853(3.7); 6.847(3.2); 6.844(3.8); 6.835(12.9); 6.829(3.4); 6.813 (4.3); 6.807(12.1); 6.790(9.6); 6.761(9.7); 6.376(1.8); 5.705(11.6); 5.702(14.8); 5.681(13.1); 5.678(10.0); 5.660(9.3); 5.657(15.9); 5.652(14.1); 5.649(8.4); 4.635(6.2); 4.590(13.5); 4.575(13.1); 1.542(62.7); 1.422(1.0); 1.370(2.1); 1.333(10.7); 1.284(16.0); 1.257(11.1); 1.232(1.0); 0.897(1.0); 0.880(3.0); 0.863(1.2); 0.146(0.6); 0.008(5.5); 0.000(190.6); 0.009 (5.5); 0.150(0.6) Example I-48: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.519(2.7); 7.296(0.5); 7.287(0.5); 7.284(0.5); 7.283(0.6); 7.282(0.7); 7.281(0.8); 7.2804(1.0); 7.2797(1.0); 7.279(0.9); 7.278(0.9); 7.2773(1.1); 7.2765(1.2); 7.276(1.3); 7.275(1.4); 7.274(1.5); 7.2733(1.6); 7.2725(1.7); 7.272(2.0); 7.271(2.1); 7.270(2.3); 7.2693(2.7); 7.2685(3.1); 7.2685(3.1); 7.268(3.4); 7.267(3.9); 7.266(4.6); 7.2653(5.6); 7.2645(6.9); 7.264(8.9); 7.260(478.6); 7.256(7.9); 7.255(5.4); 7.254(3.9); 7.253(2.7); 7.2523(2.0); 7.2515 (1.5); 7.251(1.2); 7.250(1.1); 7.249(1.0); 7.2483(0.8); 7.2475(0.7); 7.247(0.6); 7.246(0.6); 7.245(0.6); 7.210(0.9); 6.996 (2.6); 6.481(1.7); 4.830(6.4); 3.507(11.7); 3.492(12.7); 3.488(13.2); 3.473(11.9); 2.140(1.4); 2.129(1.4); 2.117(1.2); 1.966 (1.9); 1.954(2.3); 1.741(3.0); 1.735(3.7); 1.726(11.0); 1.712(14.1); 1.707(16.0); 1.698(7.4); 1.689(5.9); 1.675(7.0); 1.661 (6.0); 1.648(3.7); 1.638(4.1); 1.621(4.5); 1.606(3.0); 1.597(2.1); 1.585(1.7); 1.550(6.9); 1.455(0.9); 1.422(2.1); 1.336(2.6); 1.333(3.5); 1.284(5.1); 1.256(10.8); 0.880(1.7); 0.853(1.2); 0.837(1.1); 0.146(0.5); 0.012(0.6); 0.011(0.7); 0.008(5.7); 0.007(1.8); 0.006(1.9); 0.005(2.3); 0.004(3.0); 0.000(186.1); 0.009(4.9) Example I-495: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.519(1.0); 7.260(188.5); 6.996(1.0); 6.202(1.9); 4.565(6.5); 3.405 (10.0); 3.403(10.4); 3.391(11.2); 3.388(16.0); 3.385(11.4); 3.373(10.2); 3.371(9.8); 2.204(0.6); 2.184(2.4); 2.165(5.7); 2.147 (7.8); 2.128(6.0); 2.109(2.5); 2.090(0.5); 1.843(2.1); 1.826(4.1); 1.823(3.8); 1.814(5.5); 1.799(4.8); 1.795(6.4); 1.791 (3.9); 1.785(3.8); 1.782(4.2); 1.775(2.6); 1.771(2.2); 1.766(2.6); 1.702(1.3); 1.688(2.4); 1.683(3.8); 1.675(3.6); 1.671(4.2); 1.661(6.2); 1.654(4.0); 1.650(5.6); 1.645(6.5); 1.640(4.4); 1.630(4.1); 1.625(4.6); 1.622(5.7); 1.615(3.5); 1.610(3.3); 1.602 (7.0); 1.592(6.1); 1.582(7.3); 1.577(5.4); 1.573(5.5); 1.570(6.0); 1.563(7.7); 1.560(6.8); 1.553(3.7); 1.539(1.3); 1.533 (1.0); 1.296(2.3); 1.286(2.5); 1.280(5.2); 1.272(2.9); 1.266(4.9); 1.260(6.0); 1.248(4.9); 1.244(4.5); 1.230(4.1); 1.221(1.5); 1.214(1.5); 0.008(2.6); 0.000(76.4); 0.009(2.3) Example I-496: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.520(0.9); 7.273(0.5); 7.2722(0.6); 7.2715(0.7); 7.271(0.8); 7.270 (0.8); 7.269(0.9); 7.268(1.2); 7.2674(1.4); 7.2667(1.6); 7.266(1.9); 7.261(150.9); 7.255(1.1); 7.254(0.9); 7.253(0.8); 7.252 (0.7); 6.997(0.9); 6.221(1.5); 5.299(1.5); 4.569(5.3); 3.309(8.0); 3.307(8.2); 3.292(16.0); 3.277(8.4); 3.275(8.2); 3.007 (2.3); 2.991(2.4); 1.775(7.7); 1.772(6.8); 1.767(7.6); 1.758(6.4); 1.754(7.4); 1.748(9.5); 1.742(10.6); 1.734(8.3); 1.705(4.0); 1.702(3.7); 1.698(3.9); 1.694(3.0); 1.690(2.3); 1.686(2.0); 1.676(2.8); 1.671(2.8); 1.668(2.7); 1.664(2.2); 1.634(0.8); 1.625 (1.0); 1.617(1.4); 1.608(1.9); 1.605(1.7); 1.597(2.3); 1.588(3.2); 1.580(3.9); 1.571(3.0); 1.563(2.4); 1.560(2.3); 1.551 (2.2); 1.543(1.5); 1.534(1.1); 1.526(0.6); 1.315(0.6); 1.304(1.2); 1.296(0.8); 1.283(2.2); 1.273(3.8); 1.266(2.5); 1.250(4.7); 1.242(5.9); 1.218(4.5); 1.212(7.0); 1.191(2.7); 1.185(4.5); 1.177(2.5); 1.162(1.4); 1.160(1.4); 1.155(2.9); 1.147(1.5); 1.131 (0.7); 1.124(1.0); 1.116(0.5); 1.039(2.2); 1.032(2.5); 1.010(4.3); 1.002(5.6); 0.979(3.8); 0.975(4.0); 0.951(1.5); 0.939 (1.3); 0.927(1.0); 0.903(0.7); 0.008(2.0); 0.006(0.6); 0.005(0.7); 0.000(67.5); 0.006(0.8); 0.007(0.7); 0.009(2.1) Example I-497: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.519(1.1); 7.260(202.4); 6.996(1.1); 6.221(2.1); 4.563(7.2); 3.316 (8.4); 3.314(8.8); 3.299(16.0); 3.284(8.3); 1.822(0.6); 1.813(1.1); 1.805(1.4); 1.796(3.0); 1.785(5.7); 1.775(5.9); 1.768(9.1); 1.760(7.5); 1.754(7.2); 1.735(7.1); 1.722(5.1); 1.716(3.9); 1.706(5.0); 1.698(4.9); 1.688(4.3); 1.681(5.2); 1.674(4.7); 1.665 (4.2); 1.657(3.1); 1.638(1.8); 1.632(2.0); 1.620(3.0); 1.611(4.4); 1.604(4.5); 1.594(4.6); 1.587(6.8); 1.571(7.0); 1.558 (7.0); 1.548(4.8); 1.543(7.3); 1.534(4.6); 1.525(5.3); 1.520(7.4); 1.513(5.7); 1.505(4.0); 1.501(3.9); 1.493(5.9); 1.487(8.9); 1.479(5.6); 1.464(7.8); 1.448(2.8); 1.439(4.5); 1.432(4.2); 1.416(1.9); 1.408(2.3); 1.291(2.9); 1.284(2.7); 1.265(6.1); 1.255 (6.9); 1.247(3.9); 1.231(5.6); 1.223(3.6); 1.204(2.2); 0.008(2.8); 0.000(82.0); 0.009(2.6) Example I-504: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.518(2.3); 7.425(2.9); 7.421(3.1); 7.406(6.0); 7.402(6.6); 7.387(3.3); 7.383(3.7); 7.332(2.0); 7.327(2.1); 7.318(2.2); 7.313(4.4); 7.308(4.9); 7.299(3.5); 7.293(5.1); 7.288(3.3); 7.279(4.0); 7.274 (4.0); 7.2693(3.0); 7.2686(3.2); 7.266(4.7); 7.259(400.3); 7.253(3.6); 7.2524(2.8); 7.2516(2.1); 7.251(1.7); 7.250(1.5); 7.249(1.1); 7.2484(0.9); 7.2476(0.8); 7.247(0.6); 7.228(0.6); 7.157(5.8); 7.155(6.4); 7.139(8.9); 7.136(10.1); 7.120(4.2); 7.117(4.4); 7.106(5.1); 7.104(4.5); 7.086(4.3); 7.081(5.8); 7.078(4.7); 7.060(4.0); 7.058(3.8); 6.995(2.1); 6.575(1.8); 5.298 (1.5); 4.686(16.0); 4.671(15.6); 4.557(6.2); 1.551(2.6); 1.255(0.6); 0.049(0.8); 0.008(5.4); 0.000(176.6); 0.006 (2.1); 0.009(5.3) Example I-505: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.518(1.1); 7.357(3.1); 7.342(3.4); 7.337(5.9); 7.323(6.0); 7.318(4.5); 7.303(4.2); 7.292(0.5); 7.259(191.3); 7.250(0.9); 7.131(6.4); 7.129(6.6); 7.112(5.3); 7.110(5.6); 7.066(2.9); 7.061(4.5); 7.057(3.4); 7.042(3.0); 7.037(4.5); 7.033(3.8); 7.031(4.0); 7.023(2.2); 7.008(4.8); 7.007(4.8); 7.002(3.7); 6.995(1.5); 6.987 (2.3); 6.985(2.2); 6.981(1.8); 6.507(1.7); 5.298(1.9); 4.639(16.0); 4.625(16.0); 4.578(5.8); 1.547(15.6); 1.255(0.6); 0.008 (2.8); 0.000(80.8); 0.009(2.6) Example I-506: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.518(3.0); 7.338(9.0); 7.333(4.3); 7.325(9.6); 7.316(11.0); 7.309(4.9); 7.303(10.5); 7.259(541.9); 7.078(1.6); 7.071(12.8); 7.065(4.1); 7.054(4.2); 7.049(22.8); 7.044(4.3); 7.033(3.6); 7.027 (11.0); 7.005(0.9); 6.995(2.9); 6.456(1.8); 4.606(15.8); 4.592(16.0); 4.558(5.4); 1.535(13.5); 0.146(0.8); 0.008(7.4); 0.000 (228.6); 0.009(7.3); 0.149(0.8) Example I-509: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.518(0.8); 7.352(1.8); 7.346(11.6); 7.341(5.0); 7.330(7.0); 7.325(27.4); 7.319(5.0); 7.289(21.5); 7.284(6.6); 7.278(2.4); 7.273(4.6); 7.268(11.0); 7.259(142.7); 7.222(0.7); 6.995(0.8); 6.476 (1.6); 5.298(1.5); 4.606(15.0); 4.591(16.0); 4.574(5.4); 4.370(0.5); 1.565(0.9); 0.008(1.8); 0.000(58.2); 0.008(2.2) Example I-513: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.518(2.2); 7.294(0.5); 7.259(401.2); 7.209(0.6); 7.190(2.8); 7.187 (2.1); 7.176(4.5); 7.172(5.5); 7.163(3.1); 7.158(4.3); 7.152(3.1); 7.142(4.1); 7.139(3.9); 7.134(2.0); 7.124(4.2); 7.118(5.0); 7.113(3.1); 7.100(8.0); 7.096(5.6); 7.087(5.4); 7.084(4.8); 7.081(3.4); 7.078(4.0); 7.069(3.4); 7.065(4.3); 7.060(1.7); 7.056 (1.7); 7.048(1.3); 7.044(1.6); 6.995(2.2); 6.590(2.0); 5.298(0.6); 4.708(16.0); 4.692(15.6); 4.573(6.8); 1.540(10.8); 1.255 (1.4); 0.146(0.5); 0.008(5.3); 0.000(174.2); 0.009(5.6); 0.150(0.6) Example I-515: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.518(2.2); 7.292(0.7); 7.291(0.9); 7.272(2.0); 7.259(409.5); 7.209 (0.6); 7.134(2.8); 7.126(3.2); 7.119(3.1); 7.113(5.7); 7.106(3.5); 7.099(3.1); 7.092(3.3); 7.069(3.0); 7.058(3.5); 7.046(7.8); 7.035(8.0); 7.024(5.5); 7.012(5.5); 7.002(3.3); 6.995(4.1); 6.991(4.0); 6.983(5.2); 6.979(2.6); 6.972(4.5); 6.965(3.0); 6.960 (2.6); 6.952(1.7); 6.942(1.3); 6.594(1.9); 5.298(0.7); 4.654(16.0); 4.639(15.4); 4.577(6.4); 1.607(1.0); 1.548(3.2); 1.520 (2.7); 1.255(1.0); 0.008(5.4); 0.000(167.2); 0.009(5.4); 0.150(0.6) Example I-516: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.518(1.5); 7.324(2.2); 7.307(4.4); 7.303(4.2); 7.291(3.1); 7.286(9.1); 7.282(3.6); 7.270(6.0); 7.265(9.6); 7.259(265.2); 7.249(2.8); 7.210(0.6); 6.995(1.6); 6.962(1.3); 6.958(1.9); 6.948(11.5); 6.941(1.8); 6.937(2.0); 6.928(14.7); 6.919(2.1); 6.914(1.7); 6.908(10.1); 6.897(1.3); 6.894(1.0); 6.554(2.0); 5.298(2.5); 4.744(16.0); 4.730(15.8); 4.550(6.8); 1.548(5.0); 1.256(0.9); 0.008(3.5); 0.000(110.9); 0.009(3.4) Example I-517: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.518(1.6); 7.292(0.6); 7.283(0.5); 7.281(0.6); 7.278(0.7); 7.276(0.8); 7.273(1.1); 7.272(1.1); 7.271(1.3); 7.270(1.4); 7.269(1.6); 7.2683(1.8); 7.2676(2.0); 7.267(2.3); 7.266(2.7); 7.259(284.3); 7.209(0.7); 7.196(2.5); 7.191(2.7); 7.179(4.1); 7.172(3.3); 7.164(3.1); 7.159(5.8); 7.154(3.3); 7.150(2.6); 7.145(2.9); 7.139 (4.8); 7.133(5.3); 7.114(4.5); 7.090(2.4); 7.088(2.4); 7.087(2.8); 7.085(2.8); 7.083(2.3); 7.081(2.9); 7.079(3.2); 7.078 (2.8); 7.076(3.0); 7.074(2.8); 7.072(2.4); 7.071(2.6); 7.069(2.3); 7.065(1.9); 7.064(1.8); 7.062(1.5); 7.060(1.7); 7.058(1.7); 7.055(1.6); 7.051(1.2); 7.050(1.2); 6.995(1.6); 6.500(1.4); 4.591(16.0); 4.576(15.9); 1.655(0.8); 1.449(0.5); 1.255(1.7); 1.242(1.3); 0.010(0.7); 0.008(3.8); 0.0064(1.3); 0.0055(1.4); 0.005(1.7); 0.004(2.3); 0.000(120.3); 0.005(2.8); 0.006 (2.2); 0.007(1.8); 0.009(3.9); 0.0115(0.7); 0.0123(0.6) Example I-518: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.518(2.1); 7.318(0.5); 7.293(1.0); 7.259(386.0); 7.210(0.8); 7.139 (0.5); 6.995(2.1); 6.892(1.1); 6.880(4.5); 6.875(6.0); 6.861(5.6); 6.855(4.6); 6.844(0.9); 6.776(1.4); 6.770(2.2); 6.764(1.2); 6.754(2.6); 6.748(4.3); 6.742(2.1); 6.731(1.4); 6.726(2.2); 6.720(1.1); 6.532(1.2); 5.298(16.0); 4.624(11.0); 4.608(11.4); 4.585(4.0); 2.004(0.7); 1.532(40.5); 1.503(0.7); 1.255(1.7); 0.146(0.6); 0.008(6.0); 0.000(164.6); 0.009(5.5); 0.150 (0.5) Example I-524: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.090(0.6); 7.519(2.6); 7.260(468.1); 6.996(2.5); 6.743(1.3); 6.734 (2.4); 6.726(12.2); 6.712(3.3); 6.707(16.0); 6.704(15.9); 6.698(2.9); 6.685(11.4); 6.677(2.2); 6.668(1.1); 6.520(2.2); 5.299 (2.4); 4.683(15.9); 4.669(15.8); 4.557(7.0); 1.556(2.2); 1.427(0.6); 0.008(5.9); 0.000(189.7); 0.009(5.3); 0.150(0.6) Example I-526: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.519(1.9); 7.293(0.9); 7.260(321.7); 7.252(2.3); 7.164(2.2); 7.152 (2.2); 7.141(5.2); 7.128(5.4); 7.119(5.5); 7.106(5.4); 7.095(2.5); 7.083(2.3); 6.996(1.8); 6.905(2.8); 6.899(2.9); 6.895(2.9); 6.890(2.9); 6.882(3.7); 6.877(4.1); 6.873(4.1); 6.868(3.8); 6.860(2.3); 6.854(2.4); 6.851(2.3); 6.845(2.1); 6.582(2.2); 5.298 (0.7); 4.755(15.9); 4.753(16.0); 4.740(15.6); 4.739(15.4); 4.563(7.3); 1.540(17.5); 1.255(0.9); 0.008(4.7); 0.000(138.5); 0.009(4.5) Example I-528: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.518(2.1); 7.277(4.1); 7.260(402.6); 7.210(0.9); 7.189(1.9); 7.183 (2.0); 7.169(4.0); 7.148(4.3); 7.142(2.3); 7.134(2.2); 7.128(2.2); 6.996(4.5); 6.991(3.2); 6.979(3.4); 6.974(6.5); 6.968(4.2); 6.956(4.1); 6.951(5.8); 6.945(2.7); 6.933(2.4); 6.928(2.6); 6.584(2.4); 4.657(16.0); 4.642(15.2); 4.579(8.0); 2.005(0.6); 1.542(10.1); 1.435(0.8); 1.255(2.9); 0.008(6.0); 0.000(166.9); 0.009(4.9) Example I-53: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.518(5.0); 7.449(3.3); 7.434(5.8); 7.430(6.3); 7.416(3.2); 7.411(3.4); 7.341(1.9); 7.337(2.2); 7.328(2.5); 7.322(4.5); 7.318(3.5); 7.309(4.1); 7.302(5.4); 7.297(3.4); 7.288(3.8); 7.284(3.8); 7.280 (2.1); 7.279(2.2); 7.276(2.9); 7.2754(3.1); 7.2747(3.4); 7.274(3.5); 7.273(3.7); 7.2723(3.9); 7.2715(4.2); 7.271(4.6); 7.270 (5.5); 7.269(6.4); 7.2682(7.6); 7.2675(8.5); 7.267(9.4); 7.266(11.0); 7.265(13.2); 7.259(875.6); 7.242(1.1); 7.209(0.6); 7.167(5.5); 7.164(6.3); 7.149(9.0); 7.146(10.3); 7.130(4.1); 7.127(4.5); 7.116(5.4); 7.114(4.7); 7.096(4.6); 7.091(6.0); 7.088(5.0); 7.070(4.1); 7.067(3.9); 6.995(4.9); 6.855(2.1); 4.825(5.2); 4.717(16.0); 4.702(15.8); 2.354(0.6); 1.548(7.1); 1.333 (3.8); 1.284(5.7); 1.256(13.5); 0.880(2.8); 0.862(1.5); 0.146(1.0); 0.069(1.6); 0.008(10.9); 0.006(4.5); 0.005(5.0); 0.000 (353.7); 0.007(8.3); 0.009(13.4); 0.150(1.1) Example I-534: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.519(2.2); 7.298(3.1); 7.273(5.4); 7.260(418.5); 7.234(2.7); 6.996 (2.4); 6.987(3.6); 6.971(4.0); 6.963(6.1); 6.947(6.2); 6.939(3.7); 6.923(3.5); 6.576(2.0); 5.299(1.0); 4.610(14.5); 4.594(16.0); 4.582(6.9); 2.005(0.8); 1.543(18.9); 0.008(5.8); 0.000(158.5); 0.009(4.1) Example I-538: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.288(1.4); 7.273(1.5); 7.267(2.1); 7.264(1.6); 7.259(64.0); 7.254(1.4); 7.2534(1.5); 7.2527(1.5); 6.945(1.0); 6.939(1.4); 6.916(1.7); 6.897(1.6); 6.891(1.1); 6.876(0.7); 6.870(0.5); 6.714(1.4); 4.733(1.6); 4.615(4.9); 4.601(4.8); 2.374(16.0); 1.549(10.4); 1.258(0.6); 0.008(0.8); 0.000(26.5); 0.009(0.8) Example I-539: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.674(13.1); 7.654(15.8); 7.520(0.9); 7.477(14.4); 7.456(11.7); 7.261 (150.8); 7.037(2.2); 6.997(1.0); 6.714(1.3); 4.766(7.0); 4.730(16.0); 4.714(15.5); 2.043(1.3); 1.558(144.0); 1.258(1.3); 0.000(38.5) Example I-540: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.518(2.5); 7.379(0.8); 7.356(4.8); 7.335(5.1); 7.330(5.1); 7.309(4.7); 7.291(1.7); 7.286(1.4); 7.279(7.4); 7.259(464.8); 7.237(5.8); 7.231(0.7); 7.191(1.5); 6.995(2.6); 5.298(7.0); 4.743(5.5); 4.664(16.0); 4.648(15.8); 3.806(1.9); 3.784(1.0); 3.775(1.3); 3.073(0.7); 3.060(0.7); 1.537(67.9); 0.146(0.6); 0.032(0.5); 0.008(5.8); 0.000(192.2); 0.009(5.3); 0.150(0.6) Example I-541: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.263(5.0); 2.005(16.0); 1.583(3.3); 0.000(1.4) Example I-542: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.518(2.6); 7.449(16.0); 7.445(8.6); 7.428(11.4); 7.310(1.3); 7.293 (0.9); 7.260(452.2); 7.227(0.8); 7.216(4.9); 7.211(4.5); 7.196(4.1); 7.191(4.0); 6.996(2.7); 6.956(1.3); 5.298(0.9); 4.748(2.2); 4.620(13.8); 4.605(13.6); 4.117(1.1); 1.544(22.3); 1.243(3.1); 0.157(0.5); 0.008(4.9); 0.000(162.4); 0.009(5.2); 0.150 (0.6) Example I-543: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.518(2.4); 7.416(5.4); 7.411(5.9); 7.399(5.4); 7.393(5.7); 7.359(0.6); 7.310(1.0); 7.293(0.5); 7.259(456.3); 7.245(3.1); 7.239(3.0); 7.235(3.8); 7.229(3.7); 7.223(3.8); 7.218(3.7); 7.154(9.2); 7.132(14.2); 7.111(6.1); 6.995(2.7); 6.945(1.8); 5.298(1.0); 4.744(6.1); 4.613(16.0); 4.599(15.8); 1.539(98.7); 1.255(1.3); 0.146(0.6); 0.008(5.5); 0.000(174.0); 0.009(5.0); 0.149(0.5) Example I-594: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.519(1.4); 7.429(2.9); 7.427(2.8); 7.413(3.4); 7.411(3.5); 7.407(6.4); 7.391(6.5); 7.386(3.9); 7.370(3.6); 7.260(247.1); 7.254(0.9); 6.996(1.4); 6.897(3.0); 6.894(2.8); 6.891(3.7); 6.888(4.0); 6.876(4.5); 6.874(4.4); 6.868(12.3); 6.861(2.7); 6.856(2.7); 6.847(6.0); 6.844(6.4); 6.841(6.2); 6.835(4.2); 6.819(5.2); 6.813 (3.9); 6.562(2.0); 5.299(1.4); 4.635(16.0); 4.620(15.9); 4.574(7.1); 1.555(16.5); 0.008(3.0); 0.000(101.4); 0.009 (2.7) Example I-86: .sup.1H-NMR(400.0 MHz, d.sub.6-DMSO): = 8.206(0.7); 3.332(0.6); 3.053(1.5); 3.037(2.2); 3.021(1.6); 2.510(5.9); 2.505(12.5); 2.501(17.0); 2.496(12.0); 2.492(5.5); 2.107(16.0); 1.689(1.6); 1.662(2.0); 1.622(0.5); 1.169(0.9); 1.157 (0.8); 1.149(0.8); 1.139(0.7); 0.910(0.9); 0.885(0.7); 0.000(5.4) Example I-9: .sup.1H-NMR(400.0 MHz, d.sub.6-DMSO): = 8.473(2.2); 8.458(3.9); 8.444(2.1); 6.529(16.0); 4.093(0.7); 4.080(0.7); 3.771(2.7); 3.747(2.9); 3.729(1.7); 3.718(3.1); 3.709(1.8); 3.701(1.9); 3.691(3.4); 3.681(1.7); 3.365(2.6); 3.337(5.9); 3.316(979.4); 3.292(67.5); 3.277(2.1); 3.266(2.7); 3.217(0.9); 3.175(3.5); 3.166(1.0); 3.161(3.5); 3.157(1.9); 3.135(6.0); 3.123(7.2); 3.112(10.0); 3.108(10.5); 3.094(4.5); 3.085(4.2); 3.060(0.7); 2.675(3.7); 2.670(5.1); 2.665(3.5); 2.549(2.0); 2.540 (6.2); 2.523(18.0); 2.519(27.1); 2.510(298.3); 2.505(624.9); 2.501(853.3); 2.496(597.9); 2.492(266.0); 2.450(2.4); 2.445(3.2); 2.441(3.0); 2.406(1.0); 2.337(2.0); 2.332(4.0); 2.328(5.3); 2.323(3.8); 2.073(2.3); 1.779(4.0); 1.752(3.4); 1.598 (1.8); 1.591(1.5); 1.576(2.2); 1.565(2.9); 1.557(2.3); 1.502(0.8); 1.492(1.4); 1.476(1.4); 1.466(2.2); 1.456(1.7); 1.448 (1.4); 1.439(1.9); 1.431(1.8); 1.405(1.0); 1.288(1.0); 1.277(1.1); 1.261(2.2); 1.251(2.4); 1.233(1.6); 1.227(2.4); 1.216(1.6); 1.200(0.9); 0.146(1.0); 0.008(11.7); 0.000(351.0); 0.009(10.8); 0.051(1.0); 0.150(1.4) Example I-96: .sup.1H-NMR(400.0 MHz, d.sub.6-DMSO): = 8.788(0.7); 7.354(1.2); 7.348(0.5); 7.340(1.4); 7.332(1.7); 7.324(0.6); 7.318(1.5); 7.183(2.3); 7.177(0.6); 7.166(0.7); 7.161(3.6); 7.155(0.7); 7.144(0.6); 7.138(1.7); 6.096(2.2); 4.387(2.1); 4.372(2.1); 3.316(39.2); 2.523(0.6); 2.519(0.8); 2.510(10.8); 2.505(23.3); 2.501(32.4); 2.496(22.3); 2.492(9.7); 2.132(16.0); 0.000(0.5) Example II-10: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.837(8.6); 7.819(9.2); 7.569(2.1); 7.550(5.0); 7.532(3.5); 7.519(3.8); 7.462(6.5); 7.443(9.6); 7.424(4.5); 7.392(1.8); 7.374(4.7); 7.356(5.3); 7.340(6.9); 7.321(9.5); 7.303(4.1); 7.292(1.4); 7.260 (649.5); 7.254(3.4); 7.253(2.7); 7.252(2.5); 7.251(2.1); 7.250(1.7); 7.2494(1.5); 7.2486(1.5); 7.248(1.2); 7.247(1.2); 7.246 (1.2); 7.2454(1.1); 7.2446(1.1); 7.244(1.2); 7.243(1.1); 7.242(1.2); 7.240(1.2); 7.225(10.4); 7.207(7.2); 6.996(3.4); 6.793 (3.3); 3.910(3.0); 3.905(3.3); 3.896(3.2); 3.881(3.5); 3.877(3.7); 3.872(3.4); 3.868(3.5); 3.858(2.1); 3.848(3.9); 3.837 (2.2); 3.830(2.4); 3.820(4.4); 3.810(2.2); 3.476(3.5); 3.468(3.8); 3.452(3.8); 3.447(3.8); 3.444(4.2); 3.439(3.8); 3.424(3.6); 3.416(3.1); 3.374(11.4); 3.358(16.0); 3.342(11.4); 3.287(5.5); 3.265(6.2); 3.258(5.5); 3.236(5.6); 1.968(1.0); 1.951(1.9); 1.937(2.0); 1.928(2.8); 1.918(2.4); 1.911(3.0); 1.902(3.7); 1.898(3.5); 1.869(2.5); 1.856(2.4); 1.704(1.1); 1.694(1.8); 1.681 (2.3); 1.670(3.3); 1.660(5.8); 1.650(5.7); 1.639(3.0); 1.626(4.7); 1.615(3.3); 1.601(3.2); 1.591(2.6); 1.577(1.3); 1.566 (1.7); 1.547(37.1); 1.457(0.6); 1.441(1.3); 1.430(1.3); 1.385(1.2); 1.374(1.6); 1.361(2.8); 1.350(3.1); 1.342(1.9); 1.333(2.4); 1.328(2.7); 1.317(2.4); 1.304(1.3); 1.292(1.4); 1.284(2.2); 1.255(3.0); 0.882(1.0); 0.863(0.5); 0.146(0.6); 0.008(6.7); 0.006 (2.1); 0.005(2.9); 0.000(218.9); 0.009(6.1); 0.150(0.7) Example II-105: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.411(0.7); 7.395(0.7); 7.262(23.8); 6.880(1.6); 6.860(1.1); 6.856(0.8); 6.834(0.6); 4.669(1.9); 4.654(1.9); 3.715(16.0); 3.710(0.9); 3.702(0.6); 3.680(0.7); 2.780(1.5); 2.767(1.1); 2.763(1.7); 2.748(1.0); 0.000(8.8) Example II-106: .sup.1H-NMR(400.6 MHz, CDCl.sub.3): = 8.311(1.0); 7.520(1.8); 7.287(2.4); 7.281(2.4); 7.261(298.4); 7.238(3.6); 6.998(1.6); 6.707(2.2); 5.300(0.8); 3.364(10.5); 3.348(16.0); 3.332(11.2); 1.790(7.5); 1.783(7.7); 1.765(9.2); 1.713(3.7); 1.686(3.4); 1.652(2.1); 1.632(2.7); 1.624(3.3); 1.615(4.0); 1.607(3.6); 1.595(3.4); 1.587(3.7); 1.556(16.6); 1.319(1.7); 1.289(3.9); 1.264(4.4); 1.257(6.1); 1.225(5.0); 1.200(2.4); 1.193(3.7); 1.185(2.6); 1.162(2.7); 1.131(1.2); 1.067(2.3); 1.060(2.7); 1.030(5.4); 1.000(4.2); 0.978(1.8); 0.967(1.5); 0.038(0.6); 0.008(2.1); 0.000(71.2); 0.008(4.1) Example II-111: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.278(2.9); 7.518(2.0); 7.430(2.7); 7.426(3.0); 7.411(5.7); 7.407(6.2); 7.393(3.1); 7.388(3.4); 7.358(2.0); 7.353(1.8); 7.344(2.0); 7.339(4.1); 7.334(2.9); 7.325(3.2); 7.319(4.6); 7.314(2.6); 7.310 (1.2); 7.305(2.7); 7.300(2.4); 7.293(0.6); 7.259(374.7); 7.176(5.5); 7.173(6.2); 7.157(9.1); 7.154(10.1); 7.138(4.2); 7.135 (4.4); 7.127(5.2); 7.124(4.7); 7.107(5.4); 7.102(7.0); 7.099(6.1); 7.081(5.8); 7.078(5.4); 6.995(2.1); 5.298(1.3); 4.730 (16.0); 4.715(15.7); 4.117(0.6); 1.546(66.1); 1.246(1.7); 0.008(4.6); 0.000(145.4); 0.009(4.1) Example II-112: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.287(3.8); 7.519(0.9); 7.435(2.3); 7.414(5.4); 7.398(5.6); 7.393(3.8); 7.377(3.2); 7.260(159.4); 7.067(2.8); 6.996(1.0); 6.916(2.6); 6.914(2.4); 6.910(3.3); 6.908(3.4); 6.895(4.4); 6.888(12.4); 6.875(2.8); 6.867(9.1); 6.858(3.7); 6.842(4.5); 6.836(3.2); 4.681(16.0); 4.666(15.7); 4.643(0.9); 1.555(10.2); 0.008(2.4); 0.000(60.0); 0.008(2.0) Example II-113: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.831(3.7); 7.519(5.3); 7.310(1.3); 7.297(0.7); 7.294(0.8); 7.269(5.1); 7.260(993.6); 7.231(0.9); 7.228(1.0); 7.209(1.3); 7.198(0.5); 6.996(5.5); 6.692(1.9); 5.299(3.6); 4.234(0.6); 3.747(0.9); 3.640(0.8); 3.358(11.6); 3.341(16.0); 3.326(12.0); 1.790(6.5); 1.781(6.5); 1.759(7.4); 1.749(5.4); 1.711(2.6); 1.704(1.7); 1.684(2.3); 1.645(1.1); 1.636(1.5); 1.625(1.8); 1.616(2.3); 1.608(2.9); 1.599(2.3); 1.588(2.0); 1.579(2.1); 1.571(1.8); 1.538 (23.7); 1.318(1.2); 1.286(3.3); 1.262(4.1); 1.255(5.6); 1.224(4.8); 1.191(3.3); 1.184(2.0); 1.161(2.4); 1.153(1.2); 1.130 (0.7); 1.064(2.1); 1.056(2.2); 1.034(4.0); 1.027(5.0); 0.998(3.6); 0.974(1.3); 0.331(1.4); 0.238(0.9); 0.158(1.3); 0.146(0.9); 0.050(0.6); 0.018(0.8); 0.015(0.9); 0.0143(0.9); 0.0135(1.0); 0.011(1.9); 0.010(2.1); 0.008(11.4); 0.0064(4.0); 0.0055 (4.4); 0.005(5.4); 0.004(7.1); 0.000(360.0); 0.005(4.2); 0.006(3.4); 0.007(2.9); 0.009(10.5); 0.011(1.5); 0.012(1.0); 0.013 (0.9); 0.014(0.9); 0.016(0.7); 0.019(0.5); 0.032(0.5); 0.150(1.1) Example II-119: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.834(4.9); 7.519(5.4); 7.432(2.0); 7.410(5.2); 7.394(5.4); 7.389(3.8); 7.373(3.4); 7.288(2.1); 7.260(986.9); 7.226(0.9); 7.210(3.3); 7.050(2.9); 6.996(5.8); 6.913(2.5); 6.904(3.5); 6.892(4.4); 6.885(13.7); 6.872(2.5); 6.864(10.2); 6.855(3.9); 6.840(4.6); 6.833(3.3); 5.299(3.9); 4.675(16.0); 4.660(15.7); 3.647(1.1); 3.305(1.4); 3.247(0.8); 2.005(0.7); 1.542(26.2); 1.257(1.2); 0.331(1.5); 0.238(0.8); 0.157(1.8); 0.146(1.4); 0.008(11.3); 0.000(371.9); 0.009(13.0); 0.050(1.2); 0.149(1.2) Example II-120: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.386(3.2); 7.519(1.6); 7.310(0.5); 7.260(299.9); 7.225(0.6); 6.996 (1.7); 6.710(2.1); 5.299(0.5); 3.363(11.0); 3.347(16.0); 3.331(11.5); 1.791(6.4); 1.781(6.6); 1.770(7.0); 1.763(7.8); 1.749 (5.9); 1.716(2.4); 1.712(2.7); 1.704(1.8); 1.685(2.3); 1.648(1.1); 1.640(1.4); 1.628(1.6); 1.620(2.2); 1.611(2.7); 1.603(2.2); 1.594(1.8); 1.583(1.7); 1.574(1.3); 1.565(0.9); 1.545(22.9); 1.328(0.6); 1.318(1.1); 1.287(3.4); 1.263(3.9); 1.255(5.3); 1.224 (4.7); 1.199(1.9); 1.192(3.4); 1.185(2.1); 1.169(1.0); 1.161(2.4); 1.154(1.3); 1.139(0.5); 1.131(0.8); 1.066(2.0); 1.059 (2.2); 1.036(4.0); 1.029(5.0); 1.000(3.6); 0.976(1.3); 0.966(1.1); 0.008(3.3); 0.000(109.1); 0.009(3.8) Example II-126: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.360(3.9); 7.519(4.0); 7.432(2.2); 7.412(5.6); 7.396(5.7); 7.391(3.8); 7.375(3.3); 7.290(1.0); 7.278(1.5); 7.274(1.9); 7.271(2.9); 7.269(4.2); 7.260(747.2); 7.210(2.5); 7.140(0.7); 7.067(2.8); 6.996(4.1); 6.916(2.6); 6.913(2.5); 6.909(3.4); 6.907(3.7); 6.895(4.1); 6.887(13.9); 6.874(2.5); 6.867(9.4); 6.857(3.8); 6.841 (4.8); 6.835(3.4); 5.299(0.9); 4.681(16.0); 4.666(15.8); 1.539(139.4); 1.489(0.6); 1.255(0.6); 0.146(0.8); 0.069(1.5); 0.008(8.5); 0.000(298.8); 0.009(8.2); 0.050(1.0); 0.149(0.8) Example II-127: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.434(3.6); 7.520(0.7); 7.261(130.3); 6.997(0.7); 6.725(2.2); 3.361 (11.3); 3.344(16.0); 3.329(11.5); 1.790(6.5); 1.781(6.5); 1.772(6.1); 1.769(6.7); 1.762(7.5); 1.758(7.5); 1.749(5.6); 1.719 (2.1); 1.715(2.3); 1.712(2.5); 1.708(1.9); 1.704(1.6); 1.700(1.4); 1.684(2.2); 1.677(1.6); 1.663(0.7); 1.655(0.7); 1.646(0.9); 1.638(1.3); 1.626(1.6); 1.618(2.2); 1.609(2.7); 1.601(2.1); 1.592(1.7); 1.589(1.7); 1.581(2.2); 1.571(12.9); 1.556(0.6); 1.328 (0.6); 1.317(1.1); 1.309(0.6); 1.286(3.2); 1.279(2.1); 1.262(3.7); 1.255(5.1); 1.231(2.6); 1.223(4.6); 1.199(1.8); 1.191 (3.2); 1.184(2.0); 1.168(1.0); 1.161(2.3); 1.153(1.2); 1.130(0.7); 1.065(2.0); 1.057(2.2); 1.035(4.0); 1.028(4.9); 1.004(3.4); 0.999(3.5); 0.975(1.3); 0.965(1.0); 0.008(1.6); 0.000(50.3); 0.009(1.4) Example II-13: .sup.1H-NMR(400.1 MHz, d.sub.6-DMSO): = 9.013(0.5); 8.998(1.0); 8.984(0.5); 7.418(0.6); 7.403(1.7); 7.387(1.4); 7.364(0.8); 7.352(0.3); 7.347(0.6); 7.344(0.5); 7.332(0.6); 7.327(0.7); 7.322(0.4); 7.313(0.4); 7.308(0.3); 7.273(2.6); 7.252(2.9); 7.245(0.4); 7.218(1.3); 7.199(2.1); 7.197(2.2); 7.180(0.6); 7.177(0.9); 6.886(0.4); 6.878(3.4); 6.873(1.1); 6.862 (1.1); 6.857(3.1); 6.849(0.3); 4.500(2.2); 4.485(2.2); 4.426(2.4); 4.411(2.4); 3.721(16.0); 3.324(23.3); 2.897(0.9); 2.7393 (0.7); 2.7385(0.7); 2.517(4.7); 2.513(9.5); 2.508(12.7); 2.504(9.1); 2.499(4.3) Example II-133: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.362(4.4); 7.519(1.7); 7.432(2.2); 7.410(5.6); 7.395(5.7); 7.389(3.8); 7.374(3.3); 7.351(0.5); 7.293(0.6); 7.276(0.6); 7.273(1.0); 7.2723(1.0); 7.2715(1.1); 7.270(1.5); 7.269(1.7); 7.268(1.9); 7.260(308.9); 7.252(1.5); 7.249(0.7); 7.210(0.5); 7.077(2.9); 6.996(1.8); 6.915(2.6); 6.912(2.4); 6.909(3.3); 6.906(3.7); 6.894(4.2); 6.886(14.2); 6.882(2.7); 6.873(2.7); 6.866(9.6); 6.862(6.4); 6.856(3.9); 6.840(4.9); 6.834(3.6); 4.680(16.0); 4.665 (15.7); 3.805(0.7); 1.552(60.5); 0.008(3.4); 0.000(119.1); 0.009(3.4) Example II-134: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.519(1.4); 7.267(2.1); 7.260(251.0); 6.996(1.4); 6.705(0.8); 3.358 (4.2); 3.341(5.9); 3.326(4.3); 1.998(16.0); 1.980(16.0); 1.794(1.7); 1.786(1.9); 1.770(3.0); 1.753(2.0); 1.745(1.8); 1.709(0.9); 1.682(0.8); 1.637(0.6); 1.626(0.6); 1.617(0.9); 1.609(1.0); 1.600(0.8); 1.589(0.7); 1.580(0.7); 1.539(50.9); 1.285(1.2); 1.262(1.5); 1.254(2.2); 1.223(1.7); 1.198(0.7); 1.191(1.3); 1.183(0.7); 1.160(0.9); 1.066(0.7); 1.058(0.8); 1.036(1.5); 1.028 (1.8); 0.999(1.3); 0.008(3.0); 0.000(96.1); 0.009(2.4) Example II-14: .sup.1H-NMR(400.0 MHz, d.sub.6-DMSO): = 10.930(0.4); 10.915(0.8); 10.901(0.4); 8.312(0.4); 7.506(0.6); 7.484 (1.0); 7.468(0.9); 7.446(0.5); 7.396(0.6); 7.380(1.2); 7.365(0.7); 7.301(0.6); 7.295(0.7); 7.269(1.1); 7.262(2.8); 7.252 (0.9); 7.240(3.2); 7.128(0.5); 7.121(0.5); 7.107(0.9); 7.101(0.9); 7.087(0.6); 7.081(0.5); 6.867(3.5); 6.845(3.1); 4.904(0.4); 4.890(0.5); 4.866(2.1); 4.852(2.2); 4.396(2.4); 4.381(2.4); 3.901(2.3); 3.807(0.4); 3.790(0.5); 3.762(1.0); 3.712(16.0); 3.430 (0.5); 3.335(165.4); 3.221(0.4); 2.676(0.7); 2.671(1.0); 2.667(0.7); 2.525(2.7); 2.511(61.4); 2.507(122.6); 2.502(160.0); 2.498(117.1); 2.493(58.3); 2.333(0.7); 2.329(1.0); 2.325(0.7); 0.000(3.6) Example II-140: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.519(1.6); 7.435(0.7); 7.414(1.6); 7.398(1.6); 7.392(1.1); 7.377(0.9); 7.309(0.7); 7.269(2.1); 7.260(305.0); 7.255(1.9); 7.254(1.4); 7.253(1.0); 7.252(0.9); 7.251(0.9); 7.209(0.7); 7.060(0.8); 6.996(1.6); 6.911(0.8); 6.909(0.7); 6.905(1.0); 6.902(1.0); 6.891(1.2); 6.882(3.7); 6.877(0.8); 6.870(0.7); 6.862(2.6); 6.858 (1.7); 6.851(1.1); 6.836(1.3); 6.830(1.0); 4.677(4.5); 4.662(4.4); 3.281(0.5); 1.990(16.0); 1.973(15.9); 1.958(0.6); 1.940 (0.5); 1.538(65.0); 0.008(3.6); 0.000(114.0); 0.009(3.0) Example II-141: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.565(1.3); 7.519(3.1); 7.373(0.9); 7.298(0.5); 7.288(0.8); 7.260(561.2); 7.253(1.4); 7.252(0.8); 7.251(0.7); 7.250(0.5); 6.996(3.0); 6.702(1.9); 6.167(0.8); 5.299(4.1); 3.364(11.5); 3.348(16.0); 3.332(11.6); 1.795(4.8); 1.790(5.5); 1.781(6.1); 1.773(7.7); 1.765(7.1); 1.757(5.4); 1.748(4.9); 1.715(2.3); 1.711(2.5); 1.708(1.9); 1.704(1.6); 1.684(2.2); 1.681(2.2); 1.659(0.9); 1.650(1.0); 1.642(1.5); 1.631(1.7); 1.622(2.3); 1.614(2.8); 1.605 (2.1); 1.594(1.7); 1.585(1.8); 1.577(1.3); 1.568(1.1); 1.541(36.7); 1.329(0.7); 1.319(1.2); 1.288(3.2); 1.264(4.0); 1.256 (5.7); 1.225(4.6); 1.200(1.8); 1.192(3.4); 1.185(2.0); 1.169(1.0); 1.162(2.4); 1.154(1.2); 1.131(0.8); 1.068(2.0); 1.061(2.2); 1.039(3.9); 1.031(4.8); 1.009(3.4); 1.002(3.4); 0.979(1.2); 0.968(1.0); 0.146(0.6); 0.008(6.1); 0.000(216.9); 0.009 (6.0); 0.150(0.6) Example II-147: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.572(2.1); 7.519(1.9); 7.436(2.3); 7.415(5.3); 7.400(5.6); 7.394(3.6); 7.378(3.1); 7.310(1.0); 7.260(331.8); 7.212(0.7); 7.064(3.1); 6.996(1.9); 6.912(2.5); 6.906(3.4); 6.893(4.6); 6.886(11.7); 6.873(2.7); 6.865(8.7); 6.855(3.5); 6.839(4.1); 6.833(3.0); 6.161(1.3); 5.298(0.6); 4.682(16.0); 4.667(15.7); 1.549(12.4); 1.255(1.4); 0.331(0.5); 0.157(0.6); 0.146(0.6); 0.008(6.5); 0.000(122.9); 0.008(5.1); 0.149(0.5) Example II-148: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.334(4.7); 7.948(1.5); 7.943(10.0); 7.940(12.4); 7.936(6.0); 7.927 (3.7); 7.922(15.8); 7.919(12.2); 7.765(1.2); 7.762(1.5); 7.758(0.8); 7.750(0.6); 7.745(2.1); 7.741(1.5); 7.643(1.5); 7.640(3.0); 7.637(1.8); 7.627(2.1); 7.622(7.6); 7.617(2.7); 7.606(3.8); 7.603(6.8); 7.600(3.5); 7.554(1.9); 7.550(10.7); 7.546(4.8); 7.533(7.9); 7.530(16.0); 7.527(4.0); 7.520(1.6); 7.516(2.7); 7.512(6.5); 7.510(4.3); 7.490(1.1); 7.475(0.6); 7.472(1.1); 7.468 (0.6); 7.446(1.1); 7.444(1.6); 7.440(0.8); 7.429(1.1); 7.425(2.0); 7.421(0.6); 7.408(0.9); 7.404(0.5); 7.273(0.5); 7.268 (1.1); 7.261(173.3); 7.252(0.9); 7.251(0.8); 7.250(0.7); 7.249(0.6); 6.997(1.0); 6.783(2.2); 3.363(10.4); 3.347(15.3); 3.331 (10.6); 3.324(2.0); 3.307(2.1); 3.291(1.5); 1.803(4.6); 1.780(9.2); 1.775(9.2); 1.755(4.5); 1.746(5.2); 1.712(2.4); 1.708 (2.5); 1.701(1.9); 1.694(1.8); 1.681(2.3); 1.670(2.1); 1.661(1.3); 1.653(1.2); 1.644(1.4); 1.633(1.7); 1.624(2.3); 1.616(2.9); 1.607(2.5); 1.596(2.4); 1.587(3.0); 1.579(3.7); 1.571(4.4); 1.332(1.0); 1.320(1.1); 1.312(0.8); 1.289(3.4); 1.284(3.2); 1.275 (2.7); 1.265(4.1); 1.258(6.7); 1.233(2.8); 1.225(4.4); 1.216(2.9); 1.200(1.8); 1.193(3.5); 1.185(2.2); 1.170(1.0); 1.162 (2.4); 1.155(1.3); 1.132(0.8); 1.071(1.9); 1.063(2.1); 1.041(3.8); 1.033(4.9); 1.010(3.7); 1.004(3.7); 0.982(1.5); 0.970(1.1); 0.008(1.8); 0.005(0.6); 0.000(66.3); 0.007(1.0); 0.009(2.2) Example II-15: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.261(13.3); 3.338(0.8); 3.322(1.1); 3.306(0.8); 2.998(16.0); 1.773(0.6); 1.555(1.2); 0.000(4.7) Example II-155: .sup.1H-NMR(400.0 MHz, d.sub.6-DMSO): = 10.995(8.3); 8.655(1.7); 8.640(3.3); 8.626(1.6); 8.091(1.0); 8.084 (8.1); 8.078(3.1); 8.070(9.0); 8.067(3.9); 8.065(3.9); 8.061(9.0); 8.053(3.2); 8.048(8.1); 8.040(0.8); 7.427(1.0); 7.419(8.5); 7.414(2.5); 7.402(3.1); 7.397(16.0); 7.392(2.7); 7.380(2.5); 7.375(7.9); 7.367(0.7); 3.309(225.9); 3.151(6.2); 3.135(9.3); 3.119(6.3); 2.674(1.4); 2.670(2.0); 2.665(1.4); 2.660(0.6); 2.523(5.5); 2.518(8.4); 2.510(110.2); 2.505(235.7); 2.500 (326.7); 2.496(228.5); 2.491(102.0); 2.447(0.6); 2.337(0.6); 2.332(1.4); 2.327(2.0); 2.323(1.4); 2.318(0.7); 1.734(3.4); 1.703 (7.0); 1.672(3.9); 1.629(2.0); 1.608(1.7); 1.581(1.3); 1.573(1.2); 1.563(1.5); 1.554(1.7); 1.546(1.5); 1.536(1.3); 1.526 (1.2); 1.518(0.8); 1.258(0.7); 1.235(1.2); 1.217(2.1); 1.187(3.6); 1.166(5.3); 1.149(3.5); 1.120(1.1); 0.983(1.5); 0.953(3.5); 0.924(2.9); 0.902(1.0); 0.008(0.5); 0.000(17.7); 0.009(0.5) Example II-168: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.968(6.4); 7.791(5.7); 7.774(7.5); 7.695(9.2); 7.681(8.5); 7.663(8.5); 7.658(5.9); 7.646(5.2); 7.627(1.7); 7.519(3.3); 7.438(2.6); 7.416(5.9); 7.401(6.1); 7.395(3.9); 7.379(3.5); 7.295(0.5); 7.291 (0.7); 7.287(0.7); 7.260(620.3); 7.251(1.2); 7.245(0.5); 7.227(0.6); 7.211(1.0); 7.099(3.2); 6.996(3.4); 6.912(2.8); 6.909 (2.7); 6.906(3.5); 6.903(3.9); 6.891(4.3); 6.883(13.2); 6.877(2.6); 6.871(2.7); 6.862(7.8); 6.858(6.1); 6.851(4.1); 6.836 (5.1); 6.829(3.7); 5.298(1.9); 4.678(16.0); 4.663(15.9); 1.545(4.7); 1.256(1.1); 0.156(0.7); 0.146(0.6); 0.069(0.7); 0.008 (7.1); 0.000(241.1); 0.009(6.4); 0.149(0.7) Example II-183: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.340(3.4); 7.267(10.1); 5.300(2.6); 3.346(2.3); 3.330(3.2); 3.314(2.3); 3.123(13.5); 3.112(16.0); 1.812(0.8); 1.807(0.8); 1.804(0.8); 1.773(1.8); 1.745(0.8); 1.737(1.0); 1.282(0.7); 1.259(0.7); 1.251(1.0); 1.245(0.6); 1.219(0.8); 1.215(0.7); 1.185(0.7); 1.033(0.8); 1.026(0.9); 1.002(0.7); 0.997(0.8); 0.000(3.8) Example II-189: .sup.1H-NMR(400.0 MHz, d.sub.6-DMSO): = 8.960(0.6); 8.945(1.2); 8.932(0.6); 8.353(3.9); 7.471(0.5); 7.450 (1.1); 7.433(1.1); 7.411(0.6); 7.267(0.7); 7.261(0.7); 7.241(1.0); 7.237(1.0); 7.217(0.7); 7.211(0.7); 7.113(0.6); 7.108(0.5); 7.091(1.1); 7.087(1.0); 7.070(0.5); 7.066(0.5); 4.484(2.8); 4.469(2.8); 3.901(1.6); 3.392(0.4); 3.387(0.4); 3.370(0.8); 3.366 (0.8); 3.330(281.7); 3.303(1.4); 3.287(0.5); 3.283(0.5); 3.258(0.4); 3.112(16.0); 3.010(15.2); 2.676(0.5); 2.671(0.7); 2.667(0.6); 2.548(0.5); 2.511(44.3); 2.507(86.3); 2.502(111.9); 2.498(83.6); 2.494(43.0); 2.334(0.5); 2.329(0.6); 2.325 (0.5); 0.000(2.5) Example II-190: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.695(4.1); 7.519(5.9); 7.322(1.4); 7.260(1074.2); 7.207(3.1); 7.175 (1.3); 7.140(1.8); 6.996(5.8); 6.724(2.6); 6.597(1.6); 6.563(7.6); 6.559(6.8); 6.521(3.3); 5.932(8.4); 5.903(7.2); 4.102(2.0); 3.758(2.3); 3.712(1.1); 3.699(0.9); 3.355(9.7); 3.339(16.0); 3.323(12.0); 3.313(5.3); 3.297(3.5); 2.772(2.6); 2.756(3.8); 2.742(2.4); 2.299(0.9); 1.769(13.4); 1.708(6.1); 1.679(6.6); 1.617(7.5); 1.609(8.0); 1.600(7.8); 1.254(14.5); 1.223(9.8); 1.191 (5.6); 1.184(4.5); 1.161(3.8); 1.057(3.0); 1.027(6.8); 0.997(5.8); 0.146(1.1); 0.008(10.2); 0.000(411.5); 0.009 (25.4); 0.150(2.0) Example II-204: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.519(1.3); 7.260(241.9); 6.996(1.3); 6.801(0.7); 4.631(0.5); 4.246 (16.0); 3.369(3.5); 3.353(4.9); 3.337(3.6); 1.794(1.9); 1.777(2.7); 1.770(2.6); 1.752(1.7); 1.719(0.8); 1.715(0.9); 1.688(0.8); 1.644(0.5); 1.633(0.6); 1.624(0.8); 1.616(1.0); 1.607(0.8); 1.599(0.7); 1.587(0.7); 1.579(0.6); 1.570(0.6); 1.540(5.8); 1.294 (1.1); 1.269(1.3); 1.262(1.9); 1.230(1.6); 1.205(0.6); 1.198(1.1); 1.190(0.7); 1.167(0.8); 1.065(0.8); 1.035(1.7); 1.006 (1.2); 0.008(2.9); 0.0064(1.1); 0.0055(1.1); 0.005(1.3); 0.000(88.1); 0.009(2.7) Example II-211: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 9.216(0.5); 9.101(4.2); 8.688(1.0); 8.545(7.5); 7.263(14.8); 7.219(0.6); 7.198(1.2); 7.176(0.7); 6.819(1.5); 6.797(2.5); 6.776(1.3); 4.214(1.6); 4.208(1.8); 3.635(16.0); 3.256(0.6); 3.248(0.6); 3.168(0.6); 3.166(0.5); 3.147(0.6); 1.584(1.5); 0.000(5.9) Example II-217: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.323(2.1); 7.519(4.4); 7.438(2.3); 7.416(5.5); 7.400(5.9); 7.395(3.8); 7.379(3.4); 7.299(0.6); 7.294(0.8); 7.289(1.0); 7.270(3.4); 7.260(821.9); 7.211(0.9); 7.160(0.5); 7.054(2.6); 6.996(4.6); 6.916(2.6); 6.913(2.5); 6.909(3.4); 6.907(3.7); 6.895(4.3); 6.887(13.9); 6.882(2.5); 6.874(2.6); 6.867(9.4); 6.863(6.2); 6.857 (3.8); 6.841(4.9); 6.835(3.4); 6.247(1.3); 6.113(2.3); 5.978(1.2); 5.298(3.3); 4.680(16.0); 4.665(15.8); 4.115(0.7); 2.352 (0.6); 2.005(0.5); 1.705(0.5); 1.537(41.2); 1.254(2.2); 0.146(0.9); 0.008(8.8); 0.000(320.3); 0.009(9.7); 0.150(0.9) Example II-22: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.665(2.6); 7.520(1.4); 7.261(258.4); 7.252(1.4); 7.251(0.9); 7.250(0.8); 7.249(0.7); 7.2484(0.6); 7.2476(0.5); 7.247(0.5); 7.228(0.5); 7.211(0.5); 6.997(1.4); 6.703(1.6); 3.352(9.6); 3.336(13.5); 3.320(9.8); 2.417(6.4); 2.071(16.0); 1.788(4.7); 1.779(5.1); 1.771(6.5); 1.763(6.3); 1.755(4.9); 1.746(4.4); 1.716(1.8); 1.713(2.1); 1.709(2.2); 1.705(1.8); 1.701(1.5); 1.682(2.0); 1.679(1.9); 1.660(0.7); 1.652(0.6); 1.643(0.9); 1.635(1.2); 1.624 (1.4); 1.615(2.0); 1.607(2.4); 1.598(1.9); 1.589(1.5); 1.587(1.6); 1.578(1.9); 1.558(17.4); 1.374(4.3); 1.357(4.3); 1.333 (1.1); 1.327(0.7); 1.317(1.0); 1.308(0.6); 1.284(3.7); 1.261(3.5); 1.254(5.1); 1.215(6.9); 1.198(6.2); 1.191(3.8); 1.184(2.1); 1.168(1.0); 1.161(2.2); 1.153(1.2); 1.130(0.7); 1.063(1.7); 1.056(1.9); 1.034(3.3); 1.026(4.1); 1.003(2.9); 0.997(3.0); 0.974 (1.2); 0.963(1.0); 0.008(2.7); 0.000(105.0); 0.009(3.3) Example II-224: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.519(1.0); 7.436(2.3); 7.415(5.3); 7.399(5.4); 7.394(3.5); 7.378(3.1); 7.296(0.7); 7.292(0.7); 7.260(183.3); 7.027(2.1); 6.996(1.5); 6.902(2.6); 6.899(2.5); 6.895(3.3); 6.893(3.6); 6.881(4.1); 6.873(12.3); 6.868(2.5); 6.860(2.4); 6.852(8.6); 6.842(3.6); 6.826(4.4); 6.820(3.2); 5.298(0.6); 4.660(16.0); 4.645(15.6); 0.008(2.1); 0.000(69.4); 0.009(2.3) Example II-225: .sup.1H-NMR(400.0 MHz, d.sub.6-DMSO): = 10.302(3.9); 8.631(0.8); 8.617(1.5); 8.603(0.8); 8.312(0.6); 4.259 (1.7); 4.077(16.0); 3.929(2.7); 3.901(2.5); 3.413(0.4); 3.391(33.1); 3.377(1.0); 3.370(1.1); 3.365(1.1); 3.328(350.7); 3.293 (6.1); 3.290(5.5); 3.270(0.5); 3.142(0.6); 3.132(3.0); 3.116(4.5); 3.100(2.9); 2.676(0.8); 2.671(1.1); 2.667(0.8); 2.539 (0.6); 2.534(0.7); 2.524(2.7); 2.511(67.0); 2.507(136.1); 2.502(179.8); 2.498(133.5); 2.493(67.3); 2.467(0.5); 2.334(0.8); 2.329(1.1); 2.324(0.8); 1.719(1.9); 1.692(3.7); 1.674(2.3); 1.628(1.2); 1.606(0.9); 1.598(0.8); 1.595(0.8); 1.584(0.6); 1.574 (0.4); 1.565(0.6); 1.556(0.7); 1.546(0.8); 1.538(1.0); 1.529(0.8); 1.519(0.7); 1.511(0.6); 1.502(0.4); 1.236(0.7); 1.210 (1.1); 1.180(2.2); 1.160(2.3); 1.114(0.6); 0.970(0.8); 0.941(1.9); 0.913(1.4); 0.891(0.5); 0.880(0.4); 0.000(4.5) Example II-232: .sup.1H-NMR(400.0 MHz, d.sub.6-DMSO): = 8.460(0.6); 8.384(2.1); 8.371(4.0); 8.357(2.2); 8.312(1.4); 7.750 (7.4); 7.733(9.9); 7.729(9.1); 7.710(2.1); 7.707(2.4); 7.689(4.7); 7.670(3.3); 7.645(0.6); 7.628(0.5); 7.591(6.5); 7.572(9.5); 7.553(4.5); 7.536(1.3); 7.517(0.6); 7.421(1.5); 7.403(1.2); 7.199(1.2); 7.183(1.0); 6.514(16.0); 3.901(6.3); 3.563(0.5); 3.329 (1327.9); 3.269(5.2); 3.252(8.5); 3.235(8.6); 3.219(4.7); 3.176(0.7); 3.149(0.4); 3.049(0.6); 2.937(0.4); 2.676(2.4); 2.671 (3.2); 2.667(2.4); 2.507(388.9); 2.502(502.7); 2.498(375.4); 2.333(2.3); 2.329(3.0); 2.325(2.3); 1.714(5.2); 1.680(9.9); 1.643(6.2); 1.625(3.8); 1.599(2.6); 1.426(3.3); 1.409(8.4); 1.390(9.1); 1.373(4.6); 1.316(2.0); 1.298(2.8); 1.290(2.2); 1.281 (2.0); 1.273(1.8); 1.259(1.6); 1.236(4.3); 1.207(3.8); 1.177(5.9); 1.154(6.8); 1.134(3.2); 1.104(1.6); 1.075(0.5); 0.929 (2.5); 0.899(5.4); 0.871(4.9); 0.848(1.7); 0.000(10.5) Example II-233: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.677(1.5); 7.263(32.1); 6.728(0.7); 3.348(3.6); 3.332(5.3); 3.316(3.7); 2.626(1.0); 1.791(1.6); 1.785(1.8); 1.776(2.1); 1.768(2.7); 1.762(3.3); 1.750(2.0); 1.743(3.9); 1.738(2.0); 1.724(3.1); 1.719(1.4); 1.705(2.8); 1.686(1.6); 1.680(0.8); 1.620(0.5); 1.611(0.8); 1.603(1.0); 1.595(0.8); 1.583(5.3); 1.575(0.7); 1.480 (0.6); 1.461(1.9); 1.442(2.9); 1.428(1.1); 1.423(3.0); 1.405(1.9); 1.387(0.6); 1.283(1.1); 1.276(0.7); 1.259(1.3); 1.252 (1.7); 1.220(1.6); 1.196(0.6); 1.189(1.1); 1.182(0.7); 1.159(0.8); 1.061(0.7); 1.054(0.7); 1.031(1.3); 1.023(1.7); 1.001(1.2); 0.995(1.2); 0.973(8.0); 0.954(16.0); 0.936(6.5); 0.000(12.2) Example II-248: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.261(25.0); 3.325(1.1); 3.309(2.0); 3.293(1.1); 2.649(1.8); 2.631(6.3); 2.613(6.4); 2.595(2.0); 1.778(1.1); 1.773(1.1); 1.764(0.7); 1.753(1.2); 1.747(1.4); 1.558(0.6); 1.550(0.7); 1.279(0.5); 1.255(0.8); 1.247(0.9); 1.223(0.7); 1.216(0.9); 1.167(7.4); 1.148(16.0); 1.130(7.0); 1.009(0.8); 0.986(0.6); 0.000(11.2) Example II-249: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.519(1.2); 7.260(213.6); 6.996(1.2); 6.314(2.0); 3.841(1.0); 3.341 (8.4); 3.326(16.0); 3.310(8.6); 1.782(8.2); 1.774(8.0); 1.765(6.9); 1.761(7.7); 1.755(9.3); 1.750(9.9); 1.742(7.2); 1.708(2.8); 1.705(3.2); 1.701(2.5); 1.697(2.1); 1.682(2.5); 1.678(2.7); 1.670(2.2); 1.648(0.8); 1.640(1.0); 1.631(1.4); 1.623(1.9); 1.620 (1.8); 1.611(2.3); 1.602(3.2); 1.594(4.2); 1.585(4.1); 1.577(4.2); 1.574(4.2); 1.566(3.7); 1.557(2.3); 1.548(1.5); 1.321 (0.7); 1.309(1.3); 1.279(4.0); 1.271(3.0); 1.255(5.8); 1.248(7.1); 1.224(4.7); 1.217(7.1); 1.197(2.1); 1.190(3.6); 1.183(2.2); 1.167(1.1); 1.160(2.6); 1.152(1.4); 1.129(0.8); 1.053(2.3); 1.046(2.6); 1.023(4.6); 1.016(5.9); 0.988(4.2); 0.964(1.5); 0.954 (1.1); 0.008(2.8); 0.000(90.0); 0.009(2.5) Example II-251: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.521(0.6); 7.262(100.2); 7.230(0.5); 7.215(0.7); 7.212(0.7); 6.998 (0.6); 6.343(2.1); 6.332(2.2); 5.300(7.5); 3.328(8.1); 3.327(8.2); 3.322(3.5); 3.312(16.0); 3.296(9.1); 1.774(9.5); 1.770(9.6); 1.763(6.4); 1.744(11.7); 1.707(3.6); 1.703(4.0); 1.699(3.3); 1.696(2.9); 1.681(3.0); 1.677(3.2); 1.673(3.2); 1.637(1.0); 1.628(1.2); 1.620(1.4); 1.611(1.8); 1.608(1.7); 1.600(2.1); 1.591(2.6); 1.583(3.1); 1.574(2.4); 1.565(2.1); 1.562(2.1); 1.554 (2.0); 1.546(1.4); 1.537(1.1); 1.529(0.7); 1.306(1.3); 1.298(0.9); 1.276(4.0); 1.268(2.8); 1.251(4.9); 1.244(6.1); 1.220 (4.8); 1.214(6.9); 1.194(2.6); 1.187(3.8); 1.180(2.5); 1.164(1.5); 1.157(2.8); 1.149(1.7); 1.134(0.8); 1.126(1.0); 1.118(0.7); 1.042(2.3); 1.036(2.8); 1.006(6.3); 0.982(4.7); 0.953(1.9); 0.008(1.3); 0.000(44.4); 0.009(1.5) Example II-254: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.605(3.7); 7.522(0.7); 7.263(131.5); 7.213(1.2); 6.999(0.7); 6.343 (2.1); 6.331(2.1); 5.302(1.1); 3.324(8.3); 3.309(16.0); 3.293(8.8); 1.772(9.2); 1.770(9.2); 1.744(10.8); 1.707(2.7); 1.703(3.3); 1.699(2.5); 1.695(2.1); 1.681(2.2); 1.677(2.4); 1.673(2.4); 1.615(6.1); 1.606(2.1); 1.595(1.9); 1.585(2.4); 1.577(2.9); 1.569(2.2); 1.560(1.8); 1.557(1.8); 1.549(1.7); 1.540(1.1); 1.531(0.8); 1.304(1.2); 1.297(0.7); 1.274(3.8); 1.266(2.6); 1.249 (4.7); 1.243(5.9); 1.211(6.5); 1.192(2.1); 1.186(3.4); 1.179(2.0); 1.156(2.4); 1.148(1.2); 1.125(0.7); 1.039(2.1); 1.032 (2.6); 1.003(6.0); 0.979(4.4); 0.950(1.6); 0.008(1.5); 0.000(52.2); 0.009(1.5); 0.050(0.5) Example II-255: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.638(3.7); 7.522(0.5); 7.273(0.6); 7.272(0.6); 7.271(0.7); 7.270(0.8); 7.2694(0.9); 7.2686(1.1); 7.268(1.4); 7.267(1.8); 7.266(2.4); 7.263(88.4); 7.260(1.4); 7.259(0.9); 7.258(0.6); 7.213(0.6); 6.999(0.5); 6.346(2.2); 6.333(2.2); 5.300(1.4); 3.322(8.3); 3.307(16.0); 3.291(8.8); 1.771(9.3); 1.768(9.1); 1.747(9.6); 1.742(10.9); 1.706(2.7); 1.702(3.3); 1.698(2.4); 1.694(2.1); 1.680(2.2); 1.675(2.4); 1.672(2.4); 1.618(6.1); 1.603(1.4); 1.600 (1.3); 1.592(1.7); 1.583(2.3); 1.575(2.8); 1.566(2.1); 1.557(1.7); 1.554(1.7); 1.546(1.7); 1.537(1.1); 1.529(0.8); 1.304 (1.2); 1.296(0.7); 1.273(3.7); 1.266(2.5); 1.249(4.5); 1.242(5.7); 1.211(6.5); 1.192(2.1); 1.186(3.3); 1.179(2.0); 1.163(1.0); 1.156(2.3); 1.148(1.2); 1.125(0.7); 1.039(2.1); 1.032(2.6); 1.003(6.0); 0.979(4.3); 0.950(1.5); 0.008(1.1); 0.000(42.7); 0.009 (1.2) Example II-257: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.262(23.1); 4.090(4.4); 3.523(16.0); 3.317(1.0); 3.302(2.0); 3.286 (1.1); 1.774(1.1); 1.765(1.1); 1.746(1.3); 1.733(1.0); 1.560(2.3); 1.272(0.6); 1.248(0.7); 1.241(0.9); 1.210(0.9); 1.184(0.5); 1.010(0.7); 1.004(0.8); 0.976(0.6); 0.000(9.5) Example II-258: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.708(1.1); 7.262(36.1); 6.322(0.6); 3.314(2.4); 3.298(4.7); 3.283(2.6); 2.550(0.9); 1.772(2.4); 1.764(2.3); 1.740(2.8); 1.732(2.1); 1.696(0.9); 1.689(0.6); 1.674(0.7); 1.670(0.8); 1.587(0.7); 1.578(3.5); 1.570(1.1); 1.562(0.7); 1.553(0.6); 1.542(0.5); 1.271(8.6); 1.252(16.0); 1.239(2.2); 1.234(8.3); 1.208(2.0); 1.190 (0.7); 1.183(1.1); 1.176(0.7); 1.153(0.7); 1.038(0.7); 1.031(0.8); 1.008(1.4); 1.001(1.8); 0.973(1.3); 0.000(14.2) Example II-259: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.307(3.2); 7.519(2.1); 7.310(0.5); 7.282(0.7); 7.281(0.7); 7.280(0.6); 7.279(0.7); 7.278(0.9); 7.277(0.9); 7.276(1.0); 7.275(1.1); 7.2743(1.2); 7.2735(1.3); 7.273(1.4); 7.272(1.5); 7.271(1.7); 7.2703(1.9); 7.2695(2.2); 7.269(2.5); 7.268(2.9); 7.267(3.5); 7.2662(4.2); 7.2655(5.1); 7.260(363.6); 7.255(3.7); 7.254 (2.6); 7.2533(2.0); 7.2525(1.7); 7.252(1.5); 7.251(1.3); 7.250(1.1); 7.2493(1.0); 7.2485(0.9); 7.248(0.8); 7.247(0.7); 7.246 (0.6); 7.2453(0.5); 7.2445(0.5); 7.244(0.5); 6.996(2.1); 6.308(1.9); 3.330(8.3); 3.315(16.0); 3.299(8.7); 1.776(8.7); 1.772 (8.9); 1.752(9.5); 1.746(11.0); 1.704(3.2); 1.700(2.4); 1.697(2.0); 1.677(2.5); 1.631(0.8); 1.622(1.1); 1.613(1.5); 1.603 (1.9); 1.594(2.5); 1.585(3.1); 1.577(2.5); 1.565(2.9); 1.553(23.8); 1.309(1.3); 1.278(4.0); 1.271(2.8); 1.254(5.7); 1.247(6.3); 1.223(4.4); 1.216(6.5); 1.196(2.0); 1.189(3.5); 1.182(2.1); 1.159(2.4); 1.151(1.3); 1.128(0.7); 1.046(2.2); 1.039(2.6); 1.010 (6.0); 0.986(4.3); 0.957(1.5); 0.008(4.9); 0.006(1.9); 0.005(2.1); 0.000(154.8); 0.005(2.2); 0.006(1.7); 0.007 (1.6); 0.009(4.7); 0.150(0.5) Example II-260: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 13.205(0.5); 8.602(1.3); 7.521(0.6); 7.2743(0.5); 7.2735(0.6); 7.273 (0.6); 7.272(0.7); 7.271(0.8); 7.270(0.9); 7.2694(1.1); 7.2686(1.3); 7.268(1.6); 7.262(110.4); 7.2574(1.0); 7.2565(0.7); 6.998 (0.6); 6.325(2.0); 6.314(2.0); 5.299(0.5); 4.315(1.5); 4.313(1.5); 4.267(7.6); 3.322(8.0); 3.321(8.4); 3.306(16.0); 3.290 (8.6); 1.775(8.3); 1.767(8.1); 1.759(6.6); 1.748(9.4); 1.743(10.1); 1.735(7.3); 1.703(2.8); 1.699(3.2); 1.696(2.5); 1.692 (2.1); 1.688(1.8); 1.677(2.3); 1.673(2.6); 1.669(2.5); 1.631(0.6); 1.623(0.9); 1.614(1.3); 1.606(1.8); 1.603(1.7); 1.594(2.3); 1.585(3.8); 1.577(5.1); 1.569(3.1); 1.560(2.2); 1.557(2.1); 1.549(2.0); 1.540(1.3); 1.532(0.9); 1.315(0.6); 1.304(1.3); 1.297 (0.8); 1.274(3.9); 1.266(2.8); 1.250(4.9); 1.242(6.2); 1.212(6.7); 1.193(2.1); 1.186(3.5); 1.179(2.1); 1.163(1.1); 1.156 (2.5); 1.148(1.3); 1.125(0.8); 1.042(2.3); 1.035(2.6); 1.012(4.6); 1.005(5.9); 0.981(4.1); 0.978(4.2); 0.953(1.5); 0.942(1.0); 0.008(1.4); 0.000(45.4); 0.009(1.3) Example II-261: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.527(3.5); 7.520(0.6); 7.277(0.5); 7.276(0.6); 7.275(0.6); 7.274(0.7); 7.2733(0.8); 7.2726(0.9); 7.272(0.9); 7.271(1.0); 7.270(1.2); 7.269(1.4); 7.268(1.9); 7.267(2.2); 7.266(2.5); 7.261(111.1); 6.997(0.6); 6.350(2.5); 6.337(5.3); 6.323(4.1); 6.218(4.0); 6.205(8.5); 6.192(4.1); 6.087(2.0); 6.074(4.4); 6.060(2.1); 5.299(3.6); 3.325(8.5); 3.310(16.0); 3.294(8.7); 1.773(9.3); 1.770(9.4); 1.749(9.9); 1.744(11.3); 1.706(2.8); 1.702(3.2); 1.698(2.5); 1.694(2.1); 1.691(1.8); 1.680(2.3); 1.675(2.5); 1.672(2.5); 1.625(0.7); 1.616(1.1); 1.607(1.6); 1.604(1.6); 1.596 (2.2); 1.586(8.6); 1.579(3.9); 1.571(2.3); 1.562(1.9); 1.559(1.8); 1.550(1.7); 1.542(1.1); 1.533(0.8); 1.306(1.3); 1.298 (0.8); 1.275(4.0); 1.267(2.7); 1.251(4.9); 1.244(6.0); 1.213(6.6); 1.194(2.1); 1.187(3.4); 1.180(2.0); 1.164(1.1); 1.157(2.4); 1.149(1.2); 1.126(0.7); 1.042(2.3); 1.035(2.7); 1.006(6.1); 0.982(4.4); 0.953(1.5); 0.008(1.7); 0.006(1.0); 0.005(1.1); 0.000 (46.0); 0.009(1.3) Example II-262: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.644(4.4); 7.519(2.6); 7.267(4.1); 7.260(441.4); 7.255(3.4); 7.2543 (2.7); 7.2535(2.3); 7.253(1.5); 7.252(1.5); 7.251(1.3); 7.2503(1.2); 7.2495(1.0); 7.248(0.9); 7.247(0.7); 6.996(2.4); 6.326 (2.1); 5.299(3.3); 3.331(8.4); 3.316(16.0); 3.300(8.6); 1.780(8.1); 1.772(8.0); 1.747(9.9); 1.739(7.2); 1.703(3.2); 1.677(2.6); 1.618(1.3); 1.610(1.6); 1.598(1.9); 1.589(2.6); 1.581(3.2); 1.572(2.5); 1.561(2.3); 1.544(30.6); 1.308(1.4); 1.277(3.9); 1.254(5.3); 1.246(6.3); 1.216(6.5); 1.196(2.1); 1.189(3.5); 1.182(2.2); 1.159(2.5); 1.151(1.4); 1.128(0.7); 1.047(2.2); 1.040 (2.6); 1.010(5.8); 0.987(4.1); 0.958(1.6); 0.008(5.7); 0.000(183.8); 0.009(4.9); 0.150(0.5) Example II-263: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.424(4.3); 7.314(2.0); 7.304(2.6); 7.293(2.7); 7.284(3.1); 7.263(35.8); 7.253(2.2); 7.246(2.1); 7.229(1.2); 7.218(0.8); 7.202(0.6); 6.338(3.5); 6.229(2.1); 6.095(3.8); 5.960(2.0); 3.326(10.3); 3.310(15.7); 3.294(9.3); 1.776(15.2); 1.745(16.0); 1.706(6.5); 1.680(5.0); 1.599(12.4); 1.590(5.0); 1.581(5.0); 1.573(4.0); 1.563(3.5); 1.553(2.9); 1.545(2.2); 1.536(1.7); 1.304(3.4); 1.275(6.7); 1.250(8.1); 1.243(8.7); 1.214(8.9); 1.187(5.0); 1.156 (3.3); 1.126(1.5); 1.035(5.1); 1.006(8.2); 0.982(6.5); 0.954(2.8); 0.051(0.8); 0.041(1.1); 0.029(1.1); 0.020(1.3); 0.000 (14.2); 0.010(1.1) Example II-264: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.281(3.5); 7.518(1.8); 7.260(320.7); 7.209(0.6); 6.995(1.7); 6.285 (2.4); 6.225(2.5); 6.091(4.8); 5.956(2.5); 3.422(10.3); 3.406(16.0); 3.390(11.1); 2.186(2.4); 2.167(5.9); 2.148(8.0); 2.129 (6.3); 2.110(2.8); 2.091(0.6); 1.849(2.1); 1.835(3.9); 1.823(5.5); 1.804(6.6); 1.791(4.3); 1.775(2.6); 1.686(3.7); 1.665(6.7); 1.655(5.4); 1.650(6.9); 1.636(3.7); 1.628(5.7); 1.621(3.6); 1.608(7.3); 1.598(5.7); 1.589(6.9); 1.577(4.6); 1.569(4.6); 1.548 (9.7); 1.297(2.3); 1.280(5.1); 1.261(6.3); 1.249(5.4); 1.231(4.5); 1.214(1.6); 0.146(0.6); 0.008(4.0); 0.000(124.8); 0.009 (3.8); 0.150(0.5) Example II-265: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.649(1.1); 7.261(43.0); 6.328(0.5); 5.298(1.4); 3.321(1.8); 3.307(3.5); 3.291(1.9); 2.550(0.8); 1.781(1.1); 1.772(1.2); 1.762(2.0); 1.749(1.1); 1.746(1.3); 1.736(1.7); 1.723(1.0); 1.719(1.2); 1.713(0.8); 1.709(0.8); 1.703(1.0); 1.695(1.0); 1.685(0.9); 1.678(1.1); 1.671(1.0); 1.662(1.0); 1.654(0.7); 1.619(0.6); 1.610 (0.9); 1.603(0.9); 1.597(0.8); 1.593(0.9); 1.585(1.4); 1.570(1.5); 1.563(2.7); 1.546(0.7); 1.541(1.3); 1.532(0.9); 1.523 (1.0); 1.518(1.5); 1.511(1.2); 1.503(0.8); 1.499(0.7); 1.492(1.2); 1.484(1.8); 1.477(1.2); 1.461(1.6); 1.446(0.6); 1.436(1.0); 1.429(0.9); 1.413(0.5); 1.288(0.7); 1.272(7.2); 1.262(1.8); 1.254(16.0); 1.235(7.4); 1.228(1.6); 1.202(0.5); 0.008(0.5); 0.000 (19.1); 0.009(0.6) Example II-266: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.261(14.3); 5.298(7.4); 3.331(0.9); 3.316(1.7); 3.301(0.9); 2.650(1.8); 2.632(6.3); 2.613(6.4); 2.595(2.0); 1.788(0.5); 1.780(0.6); 1.770(1.0); 1.762(0.7); 1.755(0.7); 1.745(0.8); 1.738(0.7); 1.728(0.7); 1.592(0.6); 1.577(0.6); 1.554(1.1); 1.549(0.7); 1.525(0.7); 1.518(0.5); 1.499(0.6); 1.493(0.9); 1.484(0.5); 1.471 (0.8); 1.270(0.6); 1.260(0.7); 1.235(0.6); 1.167(7.2); 1.149(16.0); 1.131(7.0); 0.000(6.3) Example II-267: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.264(10.2); 5.301(1.1); 4.438(0.6); 4.432(0.6); 4.092(4.3); 3.539(0.5); 3.524(16.0); 3.306(0.5); 2.096(0.5); 2.073(0.6); 1.767(0.8); 1.762(0.6); 1.744(1.1); 1.551(0.6); 1.527(0.6); 1.519(0.7); 0.000(4.6) Example II-268: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.757(1.0); 7.264(27.7); 6.556(0.6); 6.542(0.6); 5.301(4.4); 4.433(1.5); 4.427(1.5); 3.564(0.9); 3.548(1.0); 3.530(1.2); 3.515(0.6); 3.346(0.7); 3.331(0.8); 3.326(0.8); 3.311(1.3); 3.297(0.6); 3.292(0.6); 3.277(0.6); 2.550(0.8); 2.094(1.1); 2.089(0.9); 2.086(0.8); 2.079(1.1); 2.072(1.4); 2.063(1.2); 2.058(0.7); 1.796 (0.6); 1.789(0.7); 1.785(0.7); 1.772(1.2); 1.765(2.1); 1.757(1.2); 1.745(2.1); 1.742(2.4); 1.739(1.8); 1.722(0.6); 1.714 (0.7); 1.605(0.9); 1.556(1.1); 1.549(1.3); 1.536(1.1); 1.525(1.6); 1.519(1.5); 1.511(1.1); 1.491(1.0); 1.482(0.9); 1.461(0.7); 1.457(0.5); 1.452(0.7); 1.298(0.6); 1.272(7.7); 1.253(16.0); 1.234(7.3); 0.000(12.4) Example II-269: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.562(4.5); 7.521(0.7); 7.273(0.5); 7.272(0.6); 7.2712(0.8); 7.2705 (0.9); 7.270(1.1); 7.269(1.3); 7.268(1.6); 7.267(1.8); 7.262(125.2); 7.2583(1.6); 7.2575(1.0); 7.257(0.7); 7.256(0.6); 7.255 (0.5); 7.212(0.8); 6.998(0.7); 6.556(2.6); 6.542(2.6); 4.427(6.4); 4.421(6.4); 3.588(1.7); 3.572(3.2); 3.554(3.4); 3.538(4.3); 3.522(2.2); 3.371(1.9); 3.352(3.3); 3.336(3.3); 3.333(3.2); 3.318(2.5); 3.301(1.5); 3.298(1.5); 2.119(1.6); 2.109(2.7); 2.101 (4.3); 2.092(4.2); 2.084(4.8); 2.079(5.3); 2.075(5.6); 2.070(5.1); 2.065(3.9); 2.058(2.1); 2.053(1.9); 2.048(1.6); 2.045 (1.5); 2.038(1.3); 1.808(1.6); 1.800(3.0); 1.795(3.0); 1.791(3.2); 1.783(2.6); 1.769(9.1); 1.762(5.4); 1.746(9.4); 1.726(2.6); 1.719(3.0); 1.711(1.9); 1.694(0.9); 1.687(1.0); 1.679(0.7); 1.603(16.0); 1.593(0.8); 1.562(4.5); 1.555(5.0); 1.539(4.5); 1.527(7.6); 1.519(6.9); 1.499(4.5); 1.490(3.8); 1.470(2.8); 1.466(2.0); 1.461(2.9); 1.437(1.2); 1.428(1.2); 1.345(0.7); 1.333 (1.0); 1.325(0.8); 1.314(1.9); 1.303(2.6); 1.291(1.4); 1.283(2.1); 1.273(2.3); 1.262(1.5); 1.252(1.3); 1.242(1.2); 0.008 (1.6); 0.006(0.5); 0.005(0.6); 0.004(0.7); 0.002(2.1); 0.000(53.7); 0.005(0.8); 0.006(0.6); 0.007(0.5); 0.008(1.5) Example II-270: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.556(6.7); 7.521(1.3); 7.312(0.5); 7.269(2.0); 7.262(228.8); 7.257 (1.8); 7.2563(1.3); 7.2555(0.8); 7.255(0.7); 7.254(0.6); 7.253(0.5); 7.230(0.6); 7.212(1.6); 6.998(1.2); 6.554(4.2); 6.540(4.1); 5.300(1.7); 4.428(10.4); 4.422(10.5); 3.587(3.0); 3.572(6.1); 3.555(6.7); 3.537(8.3); 3.522(4.4); 3.373(4.8); 3.359(5.6); 3.354(5.4); 3.339(8.8); 3.324(4.2); 3.319(4.1); 3.304(4.0); 2.133(0.5); 2.120(2.4); 2.113(4.3); 2.110(4.4); 2.102(7.1); 2.093 (7.1); 2.085(7.8); 2.077(9.0); 2.066(6.4); 2.061(3.5); 2.050(2.5); 2.046(2.4); 2.039(2.2); 1.809(2.6); 1.801(4.9); 1.796 (4.9); 1.792(5.1); 1.784(4.2); 1.769(14.8); 1.763(8.8); 1.747(15.6); 1.726(4.1); 1.720(4.9); 1.712(3.0); 1.695(1.4); 1.689 (1.6); 1.680(1.2); 1.608(16.0); 1.594(1.3); 1.562(7.3); 1.556(8.0); 1.540(7.5); 1.529(12.9); 1.520(11.3); 1.501(7.5); 1.492 (6.3); 1.472(4.6); 1.467(3.3); 1.463(4.7); 1.439(2.3); 1.430(1.9); 1.346(1.1); 1.335(1.6); 1.326(1.4); 1.315(3.0); 1.304(4.2); 1.284(3.4); 1.274(3.6); 1.263(2.4); 1.253(2.1); 1.242(1.9); 0.008(2.7); 0.006(0.7); 0.005(0.9); 0.000(97.6); 0.009 (2.8); 0.050(0.7) Example II-271: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.435(6.4); 7.521(1.4); 7.312(0.6); 7.278(0.5); 7.2773(0.5); 7.2765 (0.6); 7.276(0.6); 7.275(0.7); 7.274(0.8); 7.2733(0.8); 7.2725(0.9); 7.272(1.0); 7.271(1.2); 7.270(1.4); 7.2693(1.6); 7.2685 (2.0); 7.268(2.4); 7.267(3.0); 7.266(3.9); 7.265(5.2); 7.262(243.5); 7.259(3.6); 7.258(2.1); 7.257(1.5); 7.2563(1.2); 7.2555 (0.9); 7.255(0.8); 7.254(0.7); 7.253(0.6); 7.2523(0.6); 7.2515(0.5); 7.212(2.0); 6.998(1.4); 6.557(3.7); 6.544(3.7); 5.300 (1.5); 4.431(9.9); 4.425(9.9); 3.592(2.9); 3.577(5.8); 3.560(6.5); 3.542(7.9); 3.528(4.1); 3.377(4.6); 3.363(5.4); 3.358(5.0); 3.342(8.5); 3.328(4.0); 3.323(3.9); 3.308(3.8); 2.134(0.6); 2.125(1.9); 2.115(4.1); 2.103(7.2); 2.098(6.3); 2.087(7.1); 2.080 (9.4); 2.071(8.2); 2.066(4.8); 2.055(2.3); 2.051(2.2); 2.044(1.9); 1.811(2.3); 1.804(4.3); 1.797(4.8); 1.793(5.0); 1.784 (4.3); 1.780(6.3); 1.771(13.2); 1.760(6.8); 1.749(16.0); 1.740(7.7); 1.727(4.0); 1.719(4.7); 1.712(3.0); 1.695(1.4); 1.687 (1.6); 1.680(1.2); 1.609(4.7); 1.592(1.3); 1.564(6.9); 1.556(7.9); 1.541(7.4); 1.531(13.1); 1.522(11.4); 1.503(7.2); 1.494 (6.0); 1.474(4.6); 1.469(3.1); 1.465(4.6); 1.441(2.0); 1.432(1.9); 1.347(1.1); 1.336(1.5); 1.328(1.3); 1.317(2.9); 1.305(4.1); 1.286(3.2); 1.276(3.5); 1.265(2.2); 1.254(2.4); 1.245(1.7); 0.008(2.9); 0.006(0.6); 0.005(0.7); 0.004(1.0); 0.000(113.6); 0.009 (3.2); 0.050(0.9) Example II-272: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.391(6.2); 7.263(85.3); 7.213(0.6); 6.554(4.1); 6.542(4.1); 6.231(3.1); 6.097(6.2); 5.962(3.2); 5.301(0.7); 4.434(10.2); 4.429(10.4); 3.592(2.7); 3.576(5.4); 3.559(5.9); 3.541(7.3); 3.526(3.9); 3.367(4.1); 3.352(5.0); 3.347(5.0); 3.332(7.4); 3.317(3.8); 3.312(4.1); 3.297(3.4); 2.127(1.5); 2.100(8.0); 2.092(7.0); 2.078 (9.5); 2.073(9.2); 2.046(1.9); 1.803(4.4); 1.795(4.9); 1.791(5.1); 1.770(12.6); 1.766(10.3); 1.748(16.0); 1.725(3.6); 1.718 (4.8); 1.711(2.9); 1.694(1.3); 1.687(1.6); 1.679(1.2); 1.595(8.2); 1.562(7.3); 1.555(8.8); 1.540(7.5); 1.529(12.0); 1.520 (10.8); 1.500(6.3); 1.491(5.8); 1.470(4.1); 1.462(4.3); 1.437(1.7); 1.429(1.7); 1.335(1.6); 1.316(3.1); 1.304(4.1); 1.285 (3.3); 1.275(3.6); 1.254(2.2); 0.000(36.7) Example II-273: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.262(7.1); 1.743(0.6); 1.564(0.6); 1.530(16.0); 1.515(0.6); 0.000(3.1) Example II-274: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.264(4.4); 5.301(1.2); 1.742(0.6); 1.546(0.7); 1.530(16.0); 1.515(0.6); 0.000(1.9) Example II-274: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.759(1.0); 7.267(0.6); 7.264(29.3); 7.262(1.0); 7.261(0.6); 6.556(0.5); 6.542(0.5); 5.301(5.9); 4.433(1.4); 4.427(1.4); 3.564(0.8); 3.548(0.9); 3.530(1.1); 3.515(0.6); 3.346(0.6); 3.331(0.7); 3.326(0.7); 3.311(1.2); 3.297(0.5); 3.292(0.6); 3.277(0.5); 2.552(0.7); 2.106(0.5); 2.094(1.0); 2.089(0.8); 2.086(0.8); 2.079 (1.1); 2.072(1.3); 2.063(1.1); 2.058(0.7); 1.796(0.6); 1.789(0.6); 1.785(0.7); 1.772(1.1); 1.765(1.9); 1.762(1.4); 1.757 (1.1); 1.745(2.0); 1.742(2.2); 1.739(1.7); 1.722(0.6); 1.715(0.7); 1.606(0.8); 1.556(1.0); 1.549(1.2); 1.536(1.0); 1.525(1.4); 1.518(1.4); 1.511(1.0); 1.490(0.9); 1.482(0.8); 1.461(0.6); 1.452(0.6); 1.298(0.6); 1.272(7.6); 1.253(16.0); 1.234(7.2); 0.000 (12.8); 0.003(0.7) Example II-275: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.502(3.8); 7.521(0.9); 7.272(0.5); 7.2713(0.6); 7.2706(0.7); 7.270 (0.7); 7.269(0.9); 7.268(1.1); 7.2673(1.4); 7.2665(1.7); 7.262(157.4); 7.258(1.8); 7.257(1.1); 7.256(0.9); 7.255(0.7); 7.2543 (0.6); 7.2535(0.6); 7.212(1.3); 6.998(0.9); 6.550(2.2); 6.535(2.2); 4.428(5.6); 4.422(5.6); 3.589(1.5); 3.574(2.8); 3.555 (3.0); 3.539(3.8); 3.523(2.0); 3.370(1.6); 3.352(2.9); 3.336(2.9); 3.332(2.8); 3.317(2.2); 3.301(1.3); 3.298(1.3); 2.120(1.3); 2.110(2.4); 2.102(3.8); 2.093(3.8); 2.085(4.2); 2.077(4.9); 2.066(3.4); 2.060(1.8); 2.049(1.4); 2.046(1.3); 2.039(1.2); 1.808 (1.4); 1.801(2.6); 1.795(2.6); 1.791(2.7); 1.783(2.2); 1.769(7.8); 1.762(4.6); 1.746(8.2); 1.726(2.2); 1.720(2.6); 1.711 (1.6); 1.694(0.7); 1.688(0.9); 1.679(0.6); 1.582(16.0); 1.562(4.0); 1.555(4.4); 1.540(4.0); 1.528(6.8); 1.519(6.1); 1.499(3.9); 1.490(3.3); 1.470(2.5); 1.466(1.8); 1.461(2.5); 1.437(1.1); 1.428(1.1); 1.345(0.6); 1.334(0.9); 1.326(0.7); 1.315(1.7); 1.303 (2.3); 1.283(1.9); 1.274(2.0); 1.263(1.3); 1.252(1.1); 1.242(1.0); 0.008(1.8); 0.004(0.5); 0.002(2.0); 0.000(70.5); 0.009 (2.1); 0.050(0.6) Example II-276: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.264(12.4); 4.437(0.5); 4.432(0.5); 4.092(3.9); 3.524(16.0); 1.767 (0.7); 1.762(0.5); 1.744(0.9); 1.582(0.5); 1.527(0.5); 1.519(0.6); 0.000(5.7) Example II-277: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.547(6.7); 7.521(1.0); 7.271(1.2); 7.269(2.0); 7.262(180.7); 7.257 (1.4); 7.2564(1.1); 7.2556(0.7); 7.255(0.7); 7.254(0.7); 7.212(1.0); 6.998(1.0); 6.554(3.5); 6.539(3.5); 5.300(0.8); 4.428(8.7); 4.422(8.9); 3.588(2.6); 3.572(5.1); 3.555(5.7); 3.538(6.9); 3.523(3.7); 3.373(4.1); 3.359(4.8); 3.354(4.5); 3.339(7.5); 3.324(3.4); 3.319(3.4); 3.304(3.3); 2.120(2.1); 2.110(3.7); 2.102(6.0); 2.093(6.1); 2.085(6.6); 2.077(7.6); 2.066(5.4); 2.061 (2.9); 2.050(2.1); 2.046(2.1); 2.039(1.8); 1.809(2.2); 1.801(4.1); 1.796(4.2); 1.792(4.3); 1.783(3.5); 1.777(6.4); 1.769 (12.4); 1.763(7.4); 1.747(12.9); 1.726(3.5); 1.720(4.1); 1.711(2.5); 1.695(1.2); 1.688(1.3); 1.680(1.0); 1.609(16.0); 1.591 (0.9); 1.563(6.1); 1.556(6.6); 1.540(6.2); 1.529(10.8); 1.520(9.5); 1.501(6.3); 1.492(5.3); 1.472(3.9); 1.467(2.8); 1.463(4.0); 1.439(1.7); 1.430(1.6); 1.346(1.0); 1.334(1.3); 1.315(2.6); 1.304(3.6); 1.284(2.9); 1.274(3.0); 1.263(2.0); 1.253(1.7); 1.241 (1.5); 0.008(2.2); 0.000(82.8); 0.009(2.5) Example II-278: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.493(0.7); 7.522(1.4); 7.313(0.5); 7.276(0.5); 7.274(0.7); 7.273(0.7); 7.268(2.7); 7.267(3.4); 7.263(267.1); 7.213(2.5); 6.999(1.4); 6.565(3.7); 6.552(3.8); 4.641(0.5); 4.432(9.9); 4.426(9.9); 3.592(2.9); 3.577(5.7); 3.560(6.3); 3.542(7.7); 3.527(4.1); 3.375(4.5); 3.361(5.3); 3.355(5.2); 3.348(2.5); 3.340(8.4); 3.326 (3.8); 3.321(3.9); 3.306(3.8); 2.125(2.0); 2.115(4.3); 2.103(7.2); 2.098(6.3); 2.087(7.2); 2.080(9.5); 2.071(8.2); 2.066 (4.9); 2.055(2.3); 2.051(2.3); 2.044(2.0); 1.811(2.6); 1.803(4.7); 1.797(4.9); 1.793(5.3); 1.784(4.5); 1.780(6.4); 1.771(13.2); 1.765(9.7); 1.760(7.3); 1.748(16.0); 1.740(8.2); 1.726(4.2); 1.718(5.1); 1.711(3.3); 1.694(1.8); 1.687(2.0); 1.679(1.6); 1.605(1.1); 1.592(1.4); 1.564(7.4); 1.556(8.2); 1.541(7.6); 1.530(13.0); 1.521(11.4); 1.502(7.2); 1.493(6.0); 1.473(4.7); 1.468 (3.3); 1.464(4.6); 1.440(2.2); 1.431(2.0); 1.347(1.2); 1.335(1.6); 1.328(1.4); 1.317(3.0); 1.305(4.2); 1.285(3.3); 1.275 (3.7); 1.264(2.4); 1.254(2.7); 0.008(2.9); 0.000(110.0); 0.005(1.1); 0.006(0.9); 0.007(0.8); 0.009(3.2); 0.050(0.9) Example II-28: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.646(3.8); 7.519(2.1); 7.434(2.3); 7.412(5.7); 7.396(5.9); 7.391(4.0); 7.375(3.4); 7.293(0.7); 7.270(2.3); 7.260(388.4); 7.2524(1.1); 7.2516(1.1); 7.250(0.7); 7.061(2.7); 6.996(2.2); 6.910(2.8); 6.907(2.6); 6.903(3.5); 6.901(3.9); 6.889(4.3); 6.881(14.6); 6.868(2.7); 6.861(9.9); 6.851(4.5); 6.835(4.9); 6.829(3.7); 5.298(4.3); 4.740(0.5); 4.671(15.9); 4.656(16.0); 2.405(11.2); 2.329(1.1); 2.293(0.9); 2.004(0.6); 1.547(70.0); 1.249(1.2); 0.146(0.5); 0.008(4.7); 0.000(152.1); 0.009(4.3) Example II-280: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.513(4.6); 7.522(1.0); 7.313(0.6); 7.291(3.5); 7.274(4.4); 7.263(182.8); 7.252(4.0); 7.249(4.0); 7.245(3.6); 7.228(3.4); 7.213(1.5); 7.004(4.4); 6.999(1.2); 6.988(4.7); 6.980(7.0); 6.964(7.1); 6.956(4.5); 6.940(4.2); 6.708(2.8); 6.693(2.7); 4.622(15.5); 4.607(15.3); 1.594(16.0); 1.253(0.7); 0.008(2.1); 0.000(74.7); 0.009(2.0); 0.050(0.6) Example II-281: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.546(1.3); 7.520(0.8); 7.310(0.6); 7.292(0.9); 7.275(1.1); 7.261(114.6); 7.245(1.4); 7.228(1.0); 7.213(0.8); 7.210(0.7); 6.997(0.8); 6.994(1.0); 6.978(1.1); 6.970(1.6); 6.954(1.6); 6.946(1.1); 6.930(1.0); 6.685(0.6); 4.613(3.6); 4.598(3.7); 2.538(0.9); 1.549(11.9); 1.267(7.7); 1.248(16.0); 1.230(7.5); 0.008(1.4); 0.000(49.6); 0.009(1.7) Example II-282: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.414(4.6); 7.521(1.0); 7.311(1.9); 7.294(3.6); 7.283(0.6); 7.2824(0.6); 7.2816(0.7); 7.277(4.0); 7.276(4.0); 7.275(3.2); 7.273(4.4); 7.272(4.5); 7.271(4.1); 7.269(5.0); 7.268(5.2); 7.267(4.2); 7.266(4.5); 7.262(162.4); 7.258(5.7); 7.2574(5.3); 7.2565(5.6); 7.256(6.2); 7.255(6.1); 7.2544(5.7); 7.2535(5.3); 7.252 (5.5); 7.251(5.3); 7.250(4.0); 7.248(4.9); 7.247(4.8); 7.243(1.4); 7.2424(1.3); 7.2416(1.2); 7.241(1.1); 7.240(1.1); 7.239(1.1); 7.2383(1.1); 7.2375(1.1); 7.237(1.1); 7.236(1.1); 7.235(1.1); 7.230(4.0); 7.225(1.0); 7.223(0.9); 7.222(0.9); 7.213(1.9); 7.207(0.6); 7.200(0.6); 7.005(4.5); 6.998(1.3); 6.989(4.9); 6.981(7.3); 6.972(0.8); 6.964(7.5); 6.957(4.8); 6.948(0.6); 6.940 (4.6); 6.706(2.7); 6.693(2.8); 4.659(0.5); 4.627(15.9); 4.612(16.0); 4.581(0.7); 4.566(0.6); 4.130(0.5); 4.112(0.6); 2.046 (2.4); 1.615(3.0); 1.277(0.8); 1.259(1.9); 1.241(1.0); 0.049(0.8); 0.008(2.1); 0.007(0.7); 0.006(0.8); 0.005(1.1); 0.004 (1.6); 0.000(72.7); 0.005(1.3); 0.006(1.1); 0.007(1.0); 0.009(2.3); 0.011(0.6); 0.049(0.7) Example II-283: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.736(5.3); 7.518(10.7); 7.291(12.7); 7.265(36.3); 7.259(1757.3); 7.227 (3.8); 6.995(10.2); 6.983(4.5); 6.975(7.3); 6.959(6.9); 6.951(4.8); 6.935(4.1); 6.660(3.2); 4.617(16.0); 4.602(15.6); 2.330 (3.4); 1.535(338.0); 1.357(5.5); 1.342(4.8); 1.254(4.9); 0.146(3.1); 0.008(24.8); 0.000(728.6); 0.009(27.6) Example II-284: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.812(4.5); 7.521(0.6); 7.292(3.3); 7.275(4.5); 7.262(103.3); 7.254 (5.8); 7.245(4.4); 7.228(3.3); 6.993(4.1); 6.977(4.4); 6.969(6.9); 6.953(6.9); 6.945(4.5); 6.929(4.1); 6.692(2.7); 5.299(2.5); 4.615(16.0); 4.600(16.0); 2.299(7.4); 1.590(9.3); 1.255(0.8); 0.008(1.6); 0.000(39.1); 0.008(1.7) Example II-285: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.260(15.6); 4.626(1.1); 4.611(1.1); 2.336(16.0); 1.546(2.1); 0.000 (5.9) Example II-286: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.352(3.8); 7.520(0.5); 7.295(3.4); 7.278(4.5); 7.273(5.2); 7.270(5.7); 7.261(94.6); 7.249(3.4); 7.232(2.8); 7.000(3.7); 6.984(4.0); 6.976(6.2); 6.960(6.2); 6.952(3.7); 6.936(3.5); 6.698(2.7); 6.684(2.6); 6.221(2.4); 6.086(4.9); 5.952(2.5); 5.299(16.0); 4.624(15.3); 4.609(14.9); 1.579(10.6); 1.255(0.5); 0.008(1.9); 0.000(39.1); 0.009(1.2) Example II-287: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.681(2.0); 7.295(1.3); 7.278(1.5); 7.273(1.7); 7.270(1.8); 7.261(64.1); 7.253(1.7); 7.249(1.4); 7.231(1.2); 7.002(1.6); 6.986(1.7); 6.978(2.6); 6.962(2.7); 6.954(1.7); 6.938(1.6); 6.707(0.9); 6.695(1.0); 5.299(16.0); 4.627(5.6); 4.612(5.5); 1.567(4.8); 0.008(0.7); 0.000(24.7); 0.009(0.7) Example II-288: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.443(4.3); 7.519(1.2); 7.292(3.6); 7.286(0.6); 7.284(0.6); 7.283(0.7); 7.282(0.7); 7.2751(4.5); 7.2745(4.4); 7.273(3.8); 7.271(5.2); 7.2704(5.3); 7.2697(5.2); 7.269(5.1); 7.2672(6.0); 7.2665 (6.0); 7.266(5.4); 7.265(5.2); 7.264(5.7); 7.260(203.5); 7.256(4.6); 7.255(4.4); 7.254(4.9); 7.2533(4.8); 7.2526(4.4); 7.252 (4.2); 7.2502(4.4); 7.2495(4.1); 7.248(3.1); 7.246(3.9); 7.241(0.5); 7.229(3.4); 7.001(4.3); 6.996(1.4); 6.985(4.6); 6.977 (7.1); 6.961(7.1); 6.953(4.4); 6.937(4.2); 6.681(2.7); 6.668(2.6); 6.338(2.4); 6.325(5.0); 6.312(2.5); 6.207(4.9); 6.194(10.4); 6.181(5.1); 6.075(2.5); 6.062(5.3); 6.049(2.6); 5.298(1.4); 4.623(16.0); 4.608(15.7); 1.565(17.6); 1.255(0.5); 0.008 (2.7); 0.0063(1.1); 0.0055(1.2); 0.005(1.4); 0.000(84.3); 0.006(0.8); 0.009(2.4) Example II-289: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.427(1.0); 7.518(3.9); 7.293(4.4); 7.260(747.5); 7.251(6.6); 7.229 (4.0); 7.210(1.1); 7.002(4.6); 6.996(4.1); 6.986(5.0); 6.978(7.7); 6.962(7.7); 6.954(4.9); 6.938(4.4); 6.690(2.9); 4.623(16.0); 4.608(15.9); 3.246(5.8); 3.125(1.8); 3.107(5.8); 3.088(5.8); 3.070(2.1); 1.554(4.2); 1.433(11.5); 1.414(23.7); 1.396(10.8); 1.257(2.9); 0.026(1.0); 0.008(9.5); 0.006(3.8); 0.000(293.3); 0.007(2.6); 0.009(8.4) Example II-29: .sup.1H-NMR(400.6 MHz, CDCl.sub.3): = 7.676(1.4); 7.264(13.6); 6.733(0.8); 3.349(3.6); 3.333(5.4); 3.317(3.6); 2.607(0.9); 1.823(0.5); 1.804(3.2); 1.786(5.9); 1.767(6.7); 1.749(3.7); 1.731(1.0); 1.711(0.9); 1.707(0.9); 1.700(0.6); 1.680(0.8); 1.640(0.6); 1.631(0.9); 1.629(0.9); 1.620(1.1); 1.612(1.3); 1.603(1.4); 1.595(1.0); 1.586(0.8); 1.575(0.7); 1.284(1.2); 1.258(1.6); 1.252(2.0); 1.220(1.7); 1.196(0.6); 1.189(1.1); 1.181(0.7); 1.158(0.8); 1.060(0.8); 1.049(7.7); 1.031(16.0); 1.024(2.1); 1.012(6.9); 1.000(1.3); 0.994(1.3); 0.008(1.6); 0.006(0.7); 0.000(47.5); 0.006(0.5); 0.009(1.4) Example II-290: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.261(16.3); 6.979(0.7); 6.956(0.6); 5.298(0.6); 4.665(1.6); 4.649(1.5); 4.082(5.5); 3.518(16.0); 0.000(6.4) Example II-291: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.313(0.6); 7.518(3.0); 7.260(558.4); 7.170(2.6); 7.163(3.0); 7.157 (4.5); 7.149(4.3); 7.136(4.6); 7.122(2.2); 7.116(2.2); 7.010(3.3); 7.004(3.5); 6.995(4.1); 6.992(3.7); 6.987(7.5); 6.982(5.0); 6.969(4.7); 6.964(6.8); 6.959(2.9); 6.947(2.6); 6.941(2.5); 6.673(3.3); 4.672(16.0); 4.658(14.9); 4.115(1.2); 2.333(1.6); 1.641(1.0); 1.255(4.3); 1.246(4.1); 0.146(0.8); 0.008(6.4); 0.000(224.6); 0.009(8.1); 0.149(0.7) Example II-292: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.261(8.0); 4.674(0.8); 4.659(0.8); 2.333(16.0); 0.000(3.2) Example II-293: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.776(5.1); 7.518(5.2); 7.310(1.3); 7.259(997.1); 7.226(1.6); 7.209 (1.6); 7.170(2.4); 7.156(4.4); 7.135(4.5); 7.122(2.3); 7.116(2.3); 7.006(3.3); 7.000(3.5); 6.995(5.8); 6.988(3.2); 6.983(7.1); 6.977(4.3); 6.965(4.5); 6.960(6.5); 6.942(2.5); 6.937(2.8); 6.652(2.8); 4.666(16.0); 4.651(15.9); 4.097(2.7); 3.457(1.7); 3.434(1.7); 2.004(1.3); 1.539(15.4); 1.255(10.6); 1.247(8.3); 0.934(1.2); 0.880(1.3); 0.146(1.4); 0.008(13.0); 0.000(413.0); 0.009(12.6); 0.150(1.3) Example II-294: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 13.157(0.6); 8.578(2.0); 7.519(0.9); 7.261(167.1); 7.181(1.8); 7.175 (2.0); 7.167(2.1); 7.161(4.0); 7.153(3.0); 7.140(4.6); 7.134(2.6); 7.126(2.3); 7.120(2.2); 7.005(3.1); 6.999(3.2); 6.997(1.4); 6.988(3.3); 6.982(6.6); 6.976(4.2); 6.964(4.1); 6.959(6.1); 6.954(2.6); 6.942(2.3); 6.936(2.3); 6.677(2.8); 6.664(2.8); 4.768 (0.8); 4.668(16.0); 4.653(15.7); 4.495(0.5); 4.309(1.4); 4.306(1.5); 4.258(13.4); 1.561(1.7); 1.255(0.8); 0.008(2.0); 0.000 (66.2); 0.009(2.2) Example II-295: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.663(5.8); 7.519(1.0); 7.260(172.3); 7.180(1.8); 7.174(2.0); 7.166 (2.1); 7.160(4.1); 7.152(3.1); 7.139(4.9); 7.133(3.1); 7.125(2.6); 7.119(2.5); 7.018(0.6); 7.009(3.3); 7.004(3.4); 6.996(2.0); 6.992(3.6); 6.987(6.9); 6.981(4.4); 6.969(4.1); 6.964(6.2); 6.958(2.8); 6.946(2.4); 6.941(2.4); 6.695(2.9); 6.682(2.9); 5.298 (2.0); 4.677(16.0); 4.662(15.8); 4.592(1.9); 4.576(1.8); 1.567(2.1); 1.256(1.5); 0.008(2.1); 0.000(68.7); 0.008(2.5) Example II-296: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.266(3.8); 7.518(2.9); 7.259(523.2); 7.182(2.1); 7.176(2.0); 7.168 (2.2); 7.162(4.0); 7.142(4.7); 7.128(2.5); 7.122(2.4); 7.009(3.0); 7.003(2.9); 6.995(3.3); 6.992(3.3); 6.986(6.5); 6.980(4.3); 6.969(4.3); 6.963(6.2); 6.958(3.0); 6.946(2.4); 6.940(2.7); 6.658(3.0); 6.220(3.0); 6.085(6.0); 5.950(3.0); 4.673(15.7); 4.658 (16.0); 1.540(17.8); 1.255(1.9); 0.146(0.8); 0.008(5.9); 0.005(2.7); 0.000(209.3); 0.008(8.8); 0.150(0.7) Example II-297: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.215(0.6); 7.518(2.6); 7.259(456.3); 7.209(0.7); 7.181(2.2); 7.174 (2.4); 7.167(3.1); 7.160(4.7); 7.140(5.5); 7.133(3.2); 7.126(2.8); 7.120(2.4); 7.011(3.3); 7.005(3.6); 6.995(4.3); 6.988(7.6); 6.982(5.2); 6.970(5.0); 6.965(7.1); 6.960(3.2); 6.948(2.8); 6.942(2.6); 6.773(0.6); 6.752(0.7); 6.678(3.2); 4.677(15.9); 4.661 (16.0); 4.642(1.8); 4.581(2.7); 4.565(2.4); 3.330(4.2); 3.319(1.4); 1.255(1.5); 0.146(0.7); 0.008(5.4); 0.000(187.5); 0.009 (5.7); 0.149(0.7) Example II-298: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.519(2.0); 7.500(1.1); 7.277(0.6); 7.276(0.6); 7.274(0.8); 7.2724(1.1); 7.2716(1.2); 7.271(1.4); 7.270(1.6); 7.269(2.0); 7.2684(2.1); 7.2676(2.4); 7.267(2.8); 7.266(3.3); 7.265(4.2); 7.264(5.5); 7.260(322.1); 7.256(3.1); 7.2554(2.2); 7.2546(1.7); 7.254(1.4); 7.253(1.1); 7.252(0.9); 7.2514(0.6); 7.2506(0.5); 7.250 (0.6); 7.249(0.5); 7.210(1.4); 7.159(0.7); 7.137(0.9); 7.002(0.6); 6.996(2.5); 6.985(0.7); 6.979(1.3); 6.973(0.8); 6.961 (0.8); 6.956(1.2); 6.951(0.6); 6.934(0.5); 6.658(0.5); 4.662(3.0); 4.647(3.0); 3.386(0.8); 2.535(0.8); 1.540(13.4); 1.267(7.7); 1.249(16.0); 1.230(7.2); 1.140(0.7); 0.008(4.2); 0.006(1.1); 0.005(1.4); 0.000(140.1); 0.005(1.6); 0.006(1.3); 0.007 (1.1); 0.009(4.1); 0.050(0.6) Example II-299: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.753(5.1); 7.518(4.3); 7.259(837.6); 6.995(4.7); 6.735(10.6); 6.714 (15.7); 6.695(10.6); 6.572(3.2); 4.696(15.9); 4.681(16.0); 3.439(1.8); 1.537(152.4); 1.255(2.7); 0.008(12.9); 0.000(329.0); 0.008(15.0) Example II-300: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.670(5.1); 7.520(1.0); 7.276(0.6); 7.273(0.9); 7.270(1.3); 7.2693(1.4); 7.2685(1.6); 7.268(1.8); 7.267(2.1); 7.261(179.2); 7.256(1.5); 7.255(1.2); 7.254(0.8); 7.253(0.6); 7.252(0.5); 6.997(1.0); 6.754(1.2); 6.746(2.4); 6.737(11.5); 6.724(3.4); 6.718(15.8); 6.716(15.7); 6.710(2.9); 6.697(11.3); 6.689(2.2); 6.680 (1.1); 6.622(2.6); 6.610(2.6); 5.299(16.0); 4.706(15.5); 4.691(15.3); 4.616(0.6); 4.601(0.6); 1.562(13.3); 1.255(0.8); 0.008 (2.3); 0.000(78.9); 0.009(2.2) Example II-301: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.470(4.2); 7.520(1.1); 7.276(0.7); 7.274(0.8); 7.2733(0.9); 7.2725 (0.9); 7.272(1.0); 7.270(1.3); 7.269(1.4); 7.267(2.4); 7.261(189.8); 7.256(1.6); 7.255(1.1); 7.254(0.8); 7.253(0.7); 7.252(0.7); 6.997(1.0); 6.754(1.2); 6.746(2.4); 6.737(11.6); 6.724(3.2); 6.718(15.8); 6.716(15.9); 6.710(2.9); 6.697(11.4); 6.689 (2.2); 6.680(1.1); 6.608(2.7); 6.595(2.7); 4.701(16.0); 4.687(15.8); 1.580(16.4); 1.256(1.7); 0.008(2.4); 0.000(80.4); 0.009 (2.2) Example II-302: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.471(4.2); 7.520(1.0); 7.261(173.5); 6.997(1.0); 6.753(1.2); 6.745 (2.3); 6.736(11.6); 6.723(3.2); 6.717(15.6); 6.715(16.0); 6.709(3.0); 6.696(11.4); 6.688(2.2); 6.679(1.1); 6.605(2.6); 6.592 (2.6); 6.336(2.2); 6.323(4.7); 6.310(2.3); 6.204(4.7); 6.191(10.0); 6.178(4.9); 6.073(2.4); 6.060(5.1); 6.046(2.6); 5.299 (14.9); 4.701(15.2); 4.687(14.9); 1.578(15.2); 1.255(0.6); 0.008(2.2); 0.000(71.6); 0.009(2.0) Example II-303: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.355(1.9); 7.261(86.9); 6.753(0.7); 6.745(1.3); 6.736(6.3); 6.723(1.8); 6.717(8.5); 6.715(8.6); 6.709(1.7); 6.696(6.2); 6.687(1.3); 6.679(0.6); 6.604(1.3); 6.214(1.2); 6.080(2.5); 5.945(1.3); 5.299(16.0); 4.701(8.1); 4.687(8.2); 1.580(5.4); 0.008(1.0); 0.000(33.3); 0.009(1.0) Example II-304: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.608(5.2); 7.519(1.6); 7.260(281.6); 6.996(1.6); 6.749(1.0); 6.740 (2.2); 6.731(10.3); 6.712(15.0); 6.710(14.5); 6.691(10.1); 6.683(2.2); 6.674(1.0); 6.585(2.6); 4.692(16.0); 4.678(15.8); 2.672 (1.0); 2.294(7.2); 1.550(42.1); 1.533(1.1); 1.255(1.2); 0.008(3.9); 0.000(116.2); 0.009(4.6) Example II-305: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.260(22.7); 6.741(0.7); 6.722(1.0); 6.720(1.0); 6.701(0.7); 4.708(1.0); 4.693(1.1); 2.326(16.0); 1.540(2.8); 0.000(8.8) Example II-306: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.680(5.1); 7.520(1.1); 7.421(2.8); 7.403(3.5); 7.399(6.4); 7.383(6.7); 7.378(4.1); 7.362(3.8); 7.261(198.9); 6.997(1.1); 6.908(3.0); 6.905(2.9); 6.901(3.8); 6.899(4.2); 6.886(4.7); 6.879(14.3); 6.873(2.7); 6.866(2.9); 6.858(9.8); 6.854(6.8); 6.848(4.3); 6.832(5.5); 6.826(4.0); 6.672(2.6); 6.659(2.6); 5.299(1.3); 4.653 (16.0); 4.638(15.7); 1.568(19.4); 1.256(1.4); 0.011(0.6); 0.008(2.5); 0.000(78.2); 0.009(2.0) Example II-307: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.343(3.5); 7.520(0.9); 7.421(2.6); 7.400(6.3); 7.384(6.5); 7.378(4.0); 7.363(3.6); 7.261(164.5); 6.997(0.9); 6.906(2.8); 6.903(2.8); 6.899(3.6); 6.897(4.0); 6.885(4.6); 6.877(13.9); 6.872(2.8); 6.864(2.9); 6.856(9.3); 6.852(6.8); 6.846(4.4); 6.830(5.1); 6.824(3.8); 6.660(2.5); 6.215(2.4); 6.081(4.9); 5.947(2.5); 4.649 (15.9); 4.634(16.0); 1.574(9.5); 0.008(2.1); 0.000(63.0); 0.009(1.8) Example II-308: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.409(4.3); 7.519(1.9); 7.417(2.6); 7.396(6.2); 7.380(6.3); 7.375(4.2); 7.359(3.7); 7.310(0.6); 7.260(346.8); 6.996(1.9); 6.908(3.0); 6.905(2.8); 6.901(3.8); 6.899(4.1); 6.886(4.7); 6.879(15.1); 6.874(2.8); 6.866(2.9); 6.858(10.4); 6.849(4.3); 6.833(5.4); 6.827(4.0); 6.649(2.6); 4.649(16.0); 4.634(15.7); 1.559(36.8); 1.256(2.3); 0.027(0.8); 0.008(4.6); 0.000(133.1); 0.009(3.5) Example II-309: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.571(1.5); 7.414(0.8); 7.398(1.0); 7.397(1.1); 7.393(2.0); 7.377(2.0); 7.372(1.3); 7.356(1.1); 7.261(25.0); 6.904(0.9); 6.901(0.9); 6.897(1.2); 6.895(1.3); 6.883(1.5); 6.881(1.4); 6.875(4.5); 6.870(0.8); 6.862(0.9); 6.854(3.1); 6.850(2.1); 6.844(1.3); 6.828(1.6); 6.822(1.2); 6.666(0.9); 6.653(0.9); 6.334(0.7); 6.321 (1.5); 6.308(0.7); 6.203(1.5); 6.190(3.1); 6.177(1.5); 6.071(0.7); 6.058(1.6); 6.045(0.8); 5.298(16.0); 4.646(5.2); 4.631 (5.1); 1.621(1.6); 0.000(10.5) Example II-310: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.260(13.4); 6.884(0.6); 4.652(1.0); 4.637(1.1); 2.329(16.0); 1.548 (1.9); 0.000(5.2) Example II-311: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 16.694(3.8); 7.540(5.1); 7.519(4.4); 7.420(2.8); 7.400(5.8); 7.384(6.4); 7.363(3.7); 7.260(669.0); 6.996(3.9); 6.893(3.9); 6.873(12.7); 6.852(9.2); 6.826(5.1); 6.820(3.5); 6.627(2.8); 5.934(1.7); 4.641(16.0); 4.626(15.9); 2.672(11.0); 2.297(7.8); 2.273(9.4); 1.540(112.6); 1.255(2.3); 0.008(13.0); 0.000(258.9); 0.009 (10.8) Example II-312: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.792(4.9); 7.518(4.0); 7.416(3.1); 7.396(7.1); 7.380(6.9); 7.374(5.2); 7.359(4.9); 7.260(733.6); 6.996(4.1); 6.904(3.6); 6.896(4.4); 6.883(5.1); 6.876(14.8); 6.863(3.1); 6.855(10.3); 6.845 (4.2); 6.829(5.0); 6.823(3.6); 6.636(2.6); 4.644(16.0); 4.629(15.3); 3.385(1.4); 1.544(67.8); 1.255(2.3); 0.146(1.2); 0.008 (9.7); 0.000(290.3); 0.009(9.5) Example II-313: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.733(2.8); 7.518(3.9); 7.334(6.3); 7.321(6.9); 7.312(8.1); 7.299(8.3); 7.259(674.5); 7.076(8.5); 7.071(2.6); 7.054(15.0); 7.049(3.1); 7.038(2.6); 7.033(7.0); 6.995(3.7); 6.527(1.5); 5.298(16.0); 4.609(10.3); 4.594(10.2); 1.534(25.5); 1.246(1.4); 0.146(1.0); 0.008(9.6); 0.000(275.2); 0.009(8.7); 0.150(1.1) Example II-314: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.288(3.0); 7.518(1.3); 7.339(9.2); 7.333(4.3); 7.326(9.8); 7.317(11.3); 7.309(4.7); 7.304(10.8); 7.296(1.8); 7.259(215.4); 7.085(1.8); 7.078(13.3); 7.072(4.2); 7.061(4.5); 7.056(23.4); 7.051 (4.4); 7.040(3.6); 7.034(10.8); 7.027(1.1); 6.995(1.2); 6.556(2.1); 6.210(2.2); 6.076(4.4); 5.941(2.2); 5.298(1.8); 4.615 (16.0); 4.600(15.7); 2.330(0.6); 2.169(1.0); 2.004(1.9); 1.550(4.9); 1.254(0.6); 0.008(2.9); 0.000(86.3); 0.009(2.7) Example II-315: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.830(3.4); 7.520(0.6); 7.341(1.4); 7.334(9.2); 7.328(4.3); 7.321(9.9); 7.312(11.2); 7.304(4.7); 7.299(10.6); 7.291(1.5); 7.261(90.3); 7.078(1.8); 7.070(13.3); 7.065(4.3); 7.054(4.6); 7.048 (23.6); 7.043(4.7); 7.032(3.8); 7.027(10.9); 7.019(1.1); 6.997(0.5); 6.585(2.2); 5.298(13.4); 4.605(16.0); 4.590(15.7); 2.291 (5.4); 2.005(1.0); 1.590(3.1); 0.008(1.4); 0.000(37.5); 0.009(1.2) Example II-316: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.388(3.7); 7.518(1.4); 7.334(9.2); 7.329(4.3); 7.321(9.8); 7.312(11.3); 7.305(4.9); 7.299(10.9); 7.292(2.0); 7.259(243.9); 7.209(0.6); 7.086(1.7); 7.078(13.2); 7.073(4.2); 7.062(4.5); 7.057 (23.4); 7.052(4.5); 7.040(3.7); 7.035(10.9); 7.028(1.1); 6.995(1.3); 6.545(2.2); 4.613(16.0); 4.599(15.8); 1.552(18.7); 1.255 (0.7); 0.008(3.5); 0.000(99.4); 0.009(3.2) Example II-317: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.411(3.7); 7.518(1.1); 7.342(1.4); 7.335(9.2); 7.329(4.3); 7.322(9.8); 7.313(11.2); 7.305(4.8); 7.300(10.9); 7.292(1.7); 7.259(197.4); 7.085(1.7); 7.078(13.4); 7.072(4.2); 7.061(4.5); 7.056 (23.6); 7.051(4.4); 7.040(3.8); 7.034(11.0); 7.027(1.1); 6.995(1.1); 6.552(2.2); 6.329(2.0); 6.316(4.0); 6.303(2.0); 6.198 (3.9); 6.185(8.2); 6.172(4.1); 6.066(2.0); 6.053(4.3); 6.040(2.1); 5.298(2.0); 4.613(16.0); 4.599(15.8); 1.552(9.5); 1.256(0.5); 0.008(2.8); 0.000(80.0); 0.009(2.6) Example II-318: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.678(4.8); 7.519(0.6); 7.344(1.3); 7.336(8.8); 7.331(4.1); 7.323(9.5); 7.315(10.8); 7.307(4.4); 7.301(10.3); 7.294(1.5); 7.260(87.9); 7.084(1.7); 7.077(12.5); 7.072(4.0); 7.061(4.3); 7.056 (22.4); 7.050(4.4); 7.039(3.5); 7.034(10.3); 7.026(1.1); 6.996(0.5); 6.579(2.3); 5.297(3.2); 4.616(16.0); 4.602(15.9); 1.562 (4.2); 1.255(0.6); 0.008(1.3); 0.000(36.5); 0.009(1.3) Example II-319: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.724(4.7); 7.518(7.5); 7.353(15.4); 7.331(29.9); 7.286(28.6); 7.259 (1296.5); 6.995(7.1); 6.559(2.9); 4.610(16.0); 4.595(15.8); 1.532(72.1); 1.254(8.0); 0.008(18.8); 0.000(509.2); 0.008 (22.4) Example II-320: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.286(3.5); 7.518(0.9); 7.354(12.0); 7.338(7.8); 7.333(25.3); 7.308 (2.4); 7.290(21.5); 7.269(15.2); 7.260(147.5); 7.236(7.4); 6.996(0.8); 6.565(2.6); 6.213(2.2); 6.079(4.3); 5.944(2.2); 5.298 (1.2); 4.615(15.5); 4.601(16.0); 4.579(1.6); 2.004(0.6); 1.550(12.8); 1.254(0.8); 0.000(58.7); 0.024(2.9) Example II-321: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.722(3.4); 7.519(0.8); 7.353(2.2); 7.347(14.5); 7.342(6.0); 7.331(8.3); 7.326(30.9); 7.320(5.0); 7.292(5.1); 7.286(24.8); 7.281(7.1); 7.270(6.1); 7.265(15.8); 7.260(135.7); 6.996(0.8); 6.588 (2.0); 4.607(16.0); 4.592(15.7); 2.295(5.5); 1.568(4.4); 1.256(1.2); 0.008(2.0); 0.000(54.3); 0.009(1.7) Example II-322: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.358(1.0); 7.342(0.6); 7.337(2.2); 7.298(1.8); 7.277(0.9); 7.260(7.1); 4.616(1.2); 4.601(1.2); 2.329(16.0); 0.000(2.9) Example II-323: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.371(3.7); 7.518(1.4); 7.361(2.5); 7.355(14.8); 7.350(6.1); 7.339(8.1); 7.333(29.0); 7.328(4.9); 7.286(24.1); 7.281(8.1); 7.264(17.8); 7.259(259.9); 6.995(1.4); 6.569(2.3); 4.614(15.9); 4.599 (16.0); 1.545(13.3); 1.255(1.2); 0.008(3.8); 0.000(103.7); 0.009(3.4) Example II-324: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.667(3.9); 7.519(0.6); 7.360(2.1); 7.354(12.5); 7.349(5.2); 7.338(6.9); 7.332(25.4); 7.327(4.2); 7.294(3.6); 7.288(20.7); 7.283(6.1); 7.272(4.7); 7.267(11.4); 7.260(95.4); 6.996(0.5); 6.597 (1.9); 6.585(1.9); 5.298(16.0); 4.617(13.6); 4.603(13.7); 1.558(5.3); 0.008(1.3); 0.000(38.6); 0.008(1.4) Example II-325: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.394(3.5); 7.518(1.4); 7.360(2.1); 7.354(15.4); 7.349(6.4); 7.338(8.3); 7.333(30.6); 7.327(4.9); 7.292(4.6); 7.287(24.3); 7.281(7.7); 7.270(6.8); 7.265(16.1); 7.259(252.7); 6.995(1.3); 6.564 (2.1); 6.331(1.8); 6.318(3.9); 6.305(1.9); 6.200(3.8); 6.187(7.9); 6.173(3.9); 6.068(2.0); 6.055(4.1); 6.042(2.1); 5.297(5.7); 4.614(16.0); 4.600(15.8); 1.545(12.0); 0.008(3.6); 0.000(102.1); 0.009(3.1) Example II-326: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.519(0.7); 7.272(0.5); 7.271(0.5); 7.270(0.6); 7.269(0.6); 7.2684(0.7); 7.2677(0.9); 7.267(1.1); 7.266(1.3); 7.265(1.6); 7.260(118.0); 6.996(0.7); 6.863(1.9); 3.371(11.4); 3.355(16.0); 3.339 (11.6); 3.331(0.8); 1.799(4.6); 1.790(5.0); 1.780(7.4); 1.773(8.5); 1.769(7.4); 1.756(5.0); 1.748(5.0); 1.717(2.0); 1.714 (2.3); 1.710(2.5); 1.707(2.0); 1.703(1.6); 1.699(1.4); 1.688(1.8); 1.683(2.2); 1.680(2.2); 1.676(1.7); 1.672(1.9); 1.664(1.1); 1.655(1.1); 1.647(1.4); 1.644(1.1); 1.635(1.6); 1.627(2.2); 1.618(2.8); 1.610(2.2); 1.601(1.6); 1.599(1.6); 1.590(1.7); 1.581 (1.2); 1.573(0.9); 1.564(0.7); 1.549(29.1); 1.329(0.7); 1.319(1.1); 1.310(0.7); 1.288(3.2); 1.280(2.2); 1.264(3.7); 1.256 (5.4); 1.232(2.5); 1.225(4.5); 1.215(2.3); 1.200(1.8); 1.192(3.6); 1.185(2.1); 1.169(1.0); 1.162(2.5); 1.154(1.3); 1.131(0.8); 1.072(2.0); 1.065(2.2); 1.043(3.9); 1.035(5.0); 1.012(3.4); 1.006(3.5); 0.983(1.2); 0.972(1.0); 0.008(1.4); 0.005(0.6); 0.000 (49.1); 0.009(1.4) Example II-327: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.368(2.1); 7.519(1.6); 7.260(297.1); 6.996(1.7); 6.705(2.0); 6.591 (1.1); 6.467(1.0); 5.299(0.5); 3.362(10.4); 3.346(16.0); 3.330(10.8); 1.790(5.7); 1.781(6.1); 1.773(7.7); 1.765(7.4); 1.757 (5.7); 1.748(5.1); 1.715(2.3); 1.711(2.5); 1.704(1.6); 1.681(2.2); 1.659(0.8); 1.650(1.1); 1.642(1.4); 1.631(1.6); 1.622(2.3); 1.614(2.8); 1.605(2.1); 1.594(1.7); 1.585(1.8); 1.577(1.4); 1.568(1.3); 1.547(14.5); 1.329(0.6); 1.319(1.2); 1.288(3.2); 1.264 (3.7); 1.257(5.4); 1.225(4.5); 1.200(1.8); 1.193(3.3); 1.185(2.1); 1.170(1.0); 1.162(2.5); 1.155(1.3); 1.131(0.8); 1.068 (2.0); 1.060(2.3); 1.038(3.9); 1.030(4.9); 1.008(3.4); 1.001(3.5); 0.978(1.3); 0.968(1.1); 0.008(3.6); 0.000(116.9); 0.009 (3.3) Example II-328: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.268(0.5); 7.267(0.6); 7.266(0.7); 7.261(78.0); 6.831(1.3); 5.298(1.3); 3.358(6.0); 3.342(8.4); 3.326(6.1); 1.900(14.6); 1.893(16.0); 1.806(2.3); 1.779(4.8); 1.754(2.3); 1.746(2.7); 1.713(1.3); 1.710(1.3); 1.702(0.9); 1.695(0.8); 1.682(1.2); 1.679(1.2); 1.662(0.5); 1.645(0.6); 1.637(0.7); 1.625(0.9); 1.617(1.2); 1.608 (1.5); 1.600(1.2); 1.589(1.1); 1.580(1.4); 1.571(1.8); 1.563(1.6); 1.457(2.6); 1.443(6.5); 1.437(6.5); 1.422(2.3); 1.319 (0.7); 1.288(2.0); 1.281(1.5); 1.264(2.6); 1.257(8.1); 1.232(1.6); 1.225(2.8); 1.202(1.0); 1.195(1.8); 1.187(1.1); 1.171(0.5); 1.164(1.2); 1.156(0.6); 1.070(1.0); 1.063(1.2); 1.040(2.0); 1.033(2.7); 1.009(1.9); 1.003(2.0); 0.980(0.7); 0.970(0.6); 0.880 (0.5); 0.027(2.5); 0.008(0.9); 0.000(29.8); 0.009(0.8) Example II-329: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.269(0.6); 7.268(0.7); 7.267(0.8); 7.266(1.0); 7.2654(1.2); 7.2645 (1.6); 7.261(73.9); 7.256(0.7); 6.808(1.3); 5.298(16.0); 3.355(6.1); 3.339(8.7); 3.323(6.2); 1.806(2.1); 1.802(2.3); 1.798(2.4); 1.785(2.3); 1.777(4.8); 1.772(4.7); 1.752(2.4); 1.744(2.8); 1.711(1.3); 1.707(1.3); 1.699(0.9); 1.692(1.1); 1.680(1.3); 1.677(1.3); 1.671(1.3); 1.643(3.8); 1.638(5.2); 1.631(7.8); 1.622(6.5); 1.619(6.3); 1.612(8.1); 1.604(3.7); 1.595(1.9); 1.586 (1.3); 1.584(1.3); 1.575(1.3); 1.567(1.0); 1.558(1.0); 1.550(15.5); 1.526(1.0); 1.501(2.7); 1.455(2.7); 1.317(0.6); 1.285 (1.8); 1.278(1.3); 1.262(2.5); 1.256(4.6); 1.230(1.6); 1.222(2.9); 1.199(1.0); 1.192(1.9); 1.185(1.1); 1.169(0.5); 1.162(1.3); 1.154(0.7); 1.066(1.1); 1.058(1.2); 1.036(2.1); 1.028(2.7); 1.005(1.9); 0.999(2.0); 0.976(0.7); 0.966(0.6); 0.125(1.2); 0.008 (0.8); 0.004(0.6); 0.000(28.8); 0.009(0.9) Example II-330: .sup.1H-NMR(400.0 MHz, d.sub.6-DMSO): = 8.794(1.7); 8.780(3.3); 8.765(1.6); 7.977(14.0); 7.976(16.0); 7.973 (15.9); 7.972(14.0); 7.351(13.0); 7.349(13.2); 7.342(13.8); 7.340(13.1); 6.738(11.9); 6.734(12.0); 6.729(11.7); 6.725 (11.6); 3.387(0.5); 3.384(0.6); 3.373(0.6); 3.357(1.3); 3.322(766.5); 3.272(0.4); 3.268(0.4); 3.142(5.1); 3.126(8.3); 3.110 (5.3); 2.994(0.4); 2.710(0.5); 2.675(2.4); 2.670(3.3); 2.666(2.4); 2.540(118.3); 2.524(8.0); 2.510(190.3); 2.506(387.4); 2.501 (512.5); 2.497(380.3); 2.492(190.2); 2.456(0.6); 2.423(0.3); 2.366(0.5); 2.332(2.3); 2.328(3.2); 2.323(2.4); 2.008(0.4); 1.988(0.3); 1.730(3.4); 1.699(7.0); 1.667(3.8); 1.627(2.0); 1.606(1.6); 1.574(1.1); 1.566(1.2); 1.556(1.4); 1.548(1.6); 1.538 (1.4); 1.529(1.2); 1.520(1.1); 1.512(0.7); 1.503(0.5); 1.239(2.6); 1.212(2.2); 1.182(3.7); 1.161(3.9); 1.116(1.0); 0.974 (1.5); 0.945(3.4); 0.917(2.8); 0.894(0.9); 0.881(0.7); 0.870(0.3); 0.854(0.6); 0.008(0.4); 0.000(13.2); 0.008(0.5) Example II-332: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.519(0.7); 7.260(128.5); 6.996(0.7); 6.861(1.9); 5.298(0.8); 3.370 (11.5); 3.354(16.0); 3.339(11.7); 1.798(4.5); 1.788(4.9); 1.779(7.2); 1.772(8.4); 1.768(7.3); 1.755(4.9); 1.747(4.9); 1.713 (2.3); 1.710(2.5); 1.706(1.9); 1.702(1.6); 1.683(2.2); 1.679(2.2); 1.675(1.6); 1.671(1.8); 1.663(1.1); 1.654(1.1); 1.645(1.4); 1.634(1.6); 1.625(2.2); 1.617(2.8); 1.609(2.1); 1.600(1.6); 1.597(1.6); 1.589(1.8); 1.580(1.3); 1.572(1.0); 1.550(6.0); 1.328 (0.7); 1.318(1.1); 1.310(0.7); 1.287(3.2); 1.279(2.3); 1.263(3.9); 1.256(6.3); 1.231(2.5); 1.224(4.5); 1.199(1.8); 1.192 (3.5); 1.184(2.1); 1.168(1.0); 1.161(2.5); 1.153(1.3); 1.130(0.8); 1.072(2.0); 1.064(2.2); 1.042(3.9); 1.034(4.9); 1.011(3.4); 1.005(3.5); 0.982(1.2); 0.972(1.1); 0.008(1.5); 0.000(51.6); 0.009(1.5) Example II-334: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.261(35.2); 6.775(0.7); 3.362(2.7); 3.346(3.9); 3.330(2.7); 2.532(1.8); 1.801(1.2); 1.791(1.2); 1.782(1.8); 1.775(2.1); 1.758(1.2); 1.749(1.2); 1.715(0.6); 1.712(0.6); 1.683(1.3); 1.664(2.7); 1.646(3.7); 1.633(1.5); 1.627(2.9); 1.609(1.4); 1.602(0.7); 1.552(1.3); 1.331(0.9); 1.319(1.9); 1.311(6.1); 1.302(5.7); 1.293 (9.2); 1.284(4.6); 1.274(2.6); 1.266(1.7); 1.259(1.8); 1.227(1.2); 1.196(0.9); 1.188(0.5); 1.165(0.6); 1.062(0.6); 1.040 (1.0); 1.032(1.3); 1.009(0.9); 1.004(0.9); 0.909(0.6); 0.902(4.8); 0.897(2.3); 0.889(3.7); 0.885(16.0); 0.879(2.2); 0.874(1.8); 0.867(4.4); 0.000(14.7) Example II-335: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.662(2.3); 7.262(55.5); 6.723(1.1); 3.348(5.3); 3.332(7.6); 3.317(5.4); 2.620(1.5); 1.791(2.4); 1.785(2.7); 1.776(3.4); 1.766(4.4); 1.760(5.6); 1.751(3.8); 1.742(5.2); 1.722(2.7); 1.714(1.5); 1.710(1.5); 1.707(1.7); 1.704(1.8); 1.680(1.1); 1.640(0.5); 1.632(0.7); 1.620(0.8); 1.612(1.2); 1.603(1.5); 1.595(1.4); 1.583 (2.3); 1.567(0.8); 1.558(0.5); 1.408(1.0); 1.400(1.8); 1.395(1.6); 1.391(2.6); 1.387(3.9); 1.377(6.9); 1.368(5.6); 1.363 (3.2); 1.360(3.8); 1.352(1.9); 1.348(1.5); 1.335(0.9); 1.326(0.7); 1.316(0.8); 1.284(1.5); 1.276(1.1); 1.260(1.9); 1.252(2.6); 1.220(2.4); 1.197(0.9); 1.189(1.6); 1.182(1.0); 1.159(1.1); 1.151(0.6); 1.061(1.0); 1.054(1.1); 1.032(1.9); 1.024(2.4); 1.001 (1.6); 0.995(1.7); 0.972(0.6); 0.962(0.5); 0.933(6.0); 0.930(2.8); 0.924(1.8); 0.915(16.0); 0.908(2.9); 0.902(2.0); 0.897 (4.4); 0.008(0.7); 0.000(22.7); 0.009(0.7) Example II-337: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.488(3.0); 7.519(1.3); 7.260(237.3); 7.251(0.6); 6.996(1.3); 6.161 (1.0); 5.298(1.7); 3.851(0.7); 3.698(9.8); 3.682(16.0); 3.668(11.3); 1.833(6.4); 1.825(5.0); 1.810(11.5); 1.804(13.7); 1.790 (5.2); 1.778(5.5); 1.769(6.5); 1.762(5.3); 1.730(2.9); 1.701(3.0); 1.627(1.7); 1.348(1.3); 1.316(4.1); 1.292(4.4); 1.285(6.3); 1.261(3.0); 1.253(4.4); 1.245(3.9); 1.238(2.4); 1.222(2.2); 1.215(4.5); 1.207(2.5); 1.184(2.7); 1.145(2.5); 1.109(5.5); 1.079 (4.4); 1.054(1.2); 0.008(2.8); 0.000(97.2); 0.009(2.6) Example II-338: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.482(2.0); 8.312(2.6); 7.520(0.8); 7.261(150.1); 6.997(1.0); 6.578 (1.2); 6.453(1.2); 5.298(2.5); 3.885(1.0); 3.877(0.6); 3.864(0.6); 3.852(1.9); 3.697(9.9); 3.681(16.0); 3.667(11.2); 1.833(6.6); 1.826(5.4); 1.804(13.8); 1.790(6.0); 1.777(5.3); 1.769(6.5); 1.763(5.5); 1.733(3.0); 1.730(3.1); 1.726(2.7); 1.722(2.3); 1.719(2.1); 1.701(3.2); 1.357(0.7); 1.348(1.3); 1.340(0.9); 1.317(4.1); 1.293(4.4); 1.285(6.3); 1.261(3.1); 1.254(4.6); 1.245 (4.0); 1.238(2.5); 1.222(2.3); 1.215(4.6); 1.207(2.6); 1.192(1.3); 1.184(2.8); 1.177(1.4); 1.153(1.3); 1.145(2.4); 1.108 (5.6); 1.084(4.2); 1.079(4.5); 1.053(1.4); 1.044(0.9); 0.008(1.7); 0.000(60.0); 0.009(1.7) Example II-339: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.261(20.8); 3.362(1.8); 3.346(2.5); 3.330(1.8); 2.538(1.2); 1.800(0.7); 1.791(0.8); 1.781(1.2); 1.774(1.4); 1.757(0.8); 1.749(0.8); 1.666(1.0); 1.648(2.4); 1.643(0.9); 1.629(3.2); 1.624(1.4); 1.618(0.6); 1.610(2.9); 1.606(1.0); 1.592(1.3); 1.552(2.7); 1.386(0.6); 1.367(1.8); 1.349(2.6); 1.330(2.7); 1.316(0.5); 1.311 (1.9); 1.293(0.9); 1.266(0.6); 1.259(0.9); 1.227(0.8); 1.196(0.5); 1.040(0.6); 1.032(0.8); 1.009(0.6); 1.003(0.6); 0.918 (7.4); 0.900(16.40); 0.882(6.3); 0.000(7.9) Example II-340: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.766(2.7); 7.519(1.2); 7.269(1.3); 7.260(223.5); 7.252(1.1); 7.095 (1.2); 7.073(1.4); 6.996(1.2); 6.830(1.8); 6.825(0.5); 6.814(0.5); 6.809(1.5); 6.718(2.0); 5.298(1.6); 3.863(1.2); 3.778(9.7); 3.367(11.2); 3.351(16.0); 3.335(11.4); 1.799(4.6); 1.796(4.7); 1.789(5.3); 1.781(6.2); 1.773(7.8); 1.766(7.1); 1.756(5.5); 1.748(5.0); 1.719(2.0); 1.715(2.3); 1.711(2.5); 1.708(2.0); 1.704(1.7); 1.700(1.5); 1.684(2.3); 1.681(2.2); 1.673(1.8); 1.661 (1.0); 1.653(1.1); 1.644(1.5); 1.633(1.7); 1.624(2.3); 1.616(2.8); 1.608(2.2); 1.599(1.7); 1.596(1.7); 1.587(1.7); 1.579 (1.4); 1.570(1.1); 1.547(23.2); 1.330(0.7); 1.320(1.1); 1.310(0.7); 1.288(3.2); 1.281(2.3); 1.264(4.1); 1.257(5.9); 1.232(2.8); 1.225(4.7); 1.200(1.8); 1.193(3.5); 1.185(2.1); 1.170(1.0); 1.162(2.5); 1.154(1.3); 1.131(0.8); 1.070(2.0); 1.063(2.2); 1.040 (3.9); 1.033(4.9); 1.010(3.4); 1.004(3.5); 0.980(1.3); 0.970(1.1); 0.008(2.4); 0.000(87.1); 0.009(2.7) Example II-341: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.455(3.0); 7.519(1.8); 7.260(325.3); 6.996(1.7); 6.702(2.1); 6.379 (1.8); 6.365(3.7); 6.352(1.9); 6.247(3.7); 6.234(7.7); 6.220(3.8); 6.116(1.8); 6.102(4.0); 6.089(1.9); 5.298(1.1); 3.363(11.3); 3.347(16.0); 3.331(11.5); 1.789(6.0); 1.781(6.2); 1.771(7.0); 1.764(7.4); 1.749(5.4); 1.716(2.3); 1.712(2.5); 1.704(1.6); 1.685(2.2); 1.649(1.1); 1.641(1.5); 1.630(1.7); 1.621(2.2); 1.613(2.8); 1.604(2.1); 1.596(1.7); 1.584(1.7); 1.576(1.3); 1.568 (1.2); 1.549(55.6); 1.329(0.7); 1.319(1.1); 1.288(3.2); 1.264(4.1); 1.256(6.0); 1.225(4.7); 1.200(1.9); 1.192(3.2); 1.185 (2.0); 1.162(2.4); 1.154(1.3); 1.131(0.8); 1.067(1.9); 1.059(2.1); 1.037(4.0); 1.030(4.9); 1.001(3.5); 0.978(1.2); 0.967(1.0); 0.008(3.3); 0.000(118.8); 0.009(3.3) Example II-342: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.838(0.6); 7.262(25.9); 3.694(16.0); 3.349(1.7); 3.333(2.4); 3.317 (1.7); 2.492(1.5); 2.474(3.6); 2.457(1.9); 2.086(1.8); 2.069(2.6); 2.051(1.6); 1.795(0.7); 1.791(0.8); 1.786(0.9); 1.777(1.0); 1.769(1.2); 1.761(1.1); 1.753(0.9); 1.744(0.8); 1.577(1.7); 1.284(0.5); 1.260(0.6); 1.253(0.8); 1.221(0.8); 1.190(0.5); 1.032 (0.6); 1.024(0.8); 1.002(0.5); 0.996(0.6); 0.000(9.8) Example II-343: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 9.070(2.5); 9.029(2.5); 8.268(3.4); 8.263(3.6); 8.248(6.8); 8.243(7.0); 8.228(3.6); 8.223(3.6); 7.626(2.0); 7.621(2.2); 7.612(2.3); 7.607(4.5); 7.605(3.0); 7.602(2.9); 7.600(2.8); 7.594(3.0); 7.591 (2.9); 7.589(3.2); 7.587(4.8); 7.582(2.7); 7.573(2.7); 7.568(2.5); 7.520(1.5); 7.380(5.2); 7.377(5.8); 7.360(7.3); 7.359 (7.6); 7.342(4.4); 7.339(4.6); 7.261(280.9); 7.236(4.1); 7.233(4.0); 7.226(4.5); 7.223(4.5); 7.205(3.8); 7.202(3.8); 6.997 (1.5); 6.752(2.3); 5.298(1.6); 3.368(10.9); 3.352(16.0); 3.336(11.1); 1.808(4.5); 1.782(9.5); 1.757(4.3); 1.750(5.2); 1.711 (2.5); 1.681(2.3); 1.657(1.2); 1.648(1.4); 1.637(1.7); 1.628(2.2); 1.620(2.7); 1.611(2.2); 1.601(1.8); 1.591(1.8); 1.583(1.3); 1.574(1.1); 1.549(66.3); 1.333(0.8); 1.322(1.1); 1.291(3.4); 1.268(4.1); 1.260(5.8); 1.228(4.7); 1.203(1.8); 1.196(3.5); 1.188 (2.1); 1.165(2.3); 1.158(1.2); 1.135(0.8); 1.075(2.0); 1.067(2.3); 1.037(5.1); 1.008(3.8); 0.985(1.3); 0.975(1.1); 0.008 (3.4); 0.000(106.0); 0.009(3.4) Example II-344: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.304(4.5); 7.702(4.3); 7.699(5.2); 7.698(5.8); 7.695(5.4); 7.682(5.2); 7.678(7.7); 7.676(6.6); 7.665(4.4); 7.659(4.8); 7.655(3.5); 7.642(4.1); 7.636(4.5); 7.632(3.5); 7.540(3.5); 7.526(3.8); 7.520 (6.6); 7.506(5.9); 7.500(3.5); 7.486(3.5); 7.345(3.0); 7.343(3.2); 7.339(2.9); 7.336(2.9); 7.325(5.2); 7.322(5.3); 7.318 (5.0); 7.316(4.8); 7.304(2.5); 7.302(2.5); 7.297(2.4); 7.295(2.4); 7.261(180.6); 7.212(0.5); 6.997(1.0); 6.778(2.4); 5.298 (4.0); 3.363(10.8); 3.347(16.0); 3.331(10.8); 1.802(4.8); 1.789(4.7); 1.780(9.4); 1.775(9.2); 1.756(4.7); 1.747(5.2); 1.713 (2.5); 1.710(2.5); 1.682(2.3); 1.671(1.9); 1.662(1.1); 1.653(1.2); 1.645(1.5); 1.633(1.7); 1.624(2.3); 1.616(2.8); 1.608(2.2); 1.597(1.8); 1.588(1.8); 1.579(1.6); 1.562(37.7); 1.330(0.8); 1.320(1.1); 1.311(0.9); 1.289(3.5); 1.265(4.1); 1.257(5.7); 1.226 (4.7); 1.201(1.9); 1.193(3.5); 1.186(2.1); 1.170(1.1); 1.163(2.3); 1.155(1.2); 1.132(0.7); 1.070(2.1); 1.063(2.3); 1.041 (4.1); 1.033(5.3); 1.010(3.7); 1.004(3.8); 0.981(1.3); 0.970(1.1); 0.008(2.3); 0.000(69.2); 0.009(2.2) Example II-345: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.990(2.1); 8.941(2.6); 8.901(2.5); 8.321(0.7); 8.306(3.2); 8.298(1.5); 8.290(3.3); 8.284(6.4); 8.276(1.1); 8.268(6.0); 8.262(3.5); 8.245(3.1); 7.521(0.7); 7.313(0.5); 7.262(125.7); 7.212(1.2); 7.133(0.6); 7.127(0.7); 7.116(2.9); 7.115(3.1); 7.110(3.7); 7.097(2.9); 7.094(3.7); 7.092(4.9); 7.088(3.8); 7.075(2.5); 7.074 (2.5); 7.069(2.7); 7.068(2.7); 7.028(0.8); 7.022(0.7); 7.007(4.3); 7.001(3.8); 6.998(1.7); 6.991(1.2); 6.987(3.8); 6.981 (3.5); 6.977(4.5); 6.971(3.9); 6.956(3.5); 6.950(3.1); 6.744(2.5); 5.298(5.7); 3.366(10.7); 3.350(16.0); 3.338(3.6); 3.334 (10.8); 1.804(5.4); 1.782(10.7); 1.777(10.6); 1.757(5.4); 1.749(6.0); 1.715(2.9); 1.711(2.9); 1.703(2.1); 1.684(2.8); 1.672 (2.3); 1.664(1.5); 1.655(1.4); 1.646(1.8); 1.635(2.0); 1.626(2.6); 1.618(3.2); 1.609(2.6); 1.601(2.3); 1.590(2.7); 1.571(5.6); 1.332(0.9); 1.322(1.4); 1.313(1.0); 1.290(3.9); 1.267(4.9); 1.259(6.8); 1.227(5.8); 1.203(2.1); 1.195(3.9); 1.188(2.3); 1.172 (1.2); 1.165(2.6); 1.157(1.4); 1.142(0.5); 1.134(0.8); 1.126(0.5); 1.073(2.4); 1.066(2.6); 1.043(4.6); 1.036(5.9); 1.013 (4.3); 1.007(4.4); 0.984(1.6); 0.973(1.3); 0.008(1.6); 0.000(50.2); 0.009(1.8) Example II-346: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.246(4.8); 7.733(9.0); 7.730(9.9); 7.723(9.5); 7.720(9.9); 7.640(9.8); 7.637(9.7); 7.627(10.6); 7.625(9.9); 7.521(0.6); 7.262(100.6); 7.182(10.2); 7.173(10.2); 7.170(10.2); 7.160(9.4); 6.998 (0.6); 6.798(2.5); 5.298(14.3); 3.357(10.8); 3.341(16.0); 3.325(10.9); 1.798(4.6); 1.784(4.6); 1.776(9.2); 1.771(9.0); 1.752 (4.5); 1.743(5.1); 1.710(2.4); 1.706(2.5); 1.698(1.7); 1.679(2.3); 1.657(1.1); 1.648(1.1); 1.639(1.5); 1.628(1.7); 1.619 (2.3); 1.611(2.9); 1.602(2.4); 1.584(22.6); 1.574(1.7); 1.566(0.9); 1.326(0.7); 1.316(1.1); 1.308(0.8); 1.285(3.4); 1.261(4.1); 1.254(5.6); 1.222(4.7); 1.197(1.8); 1.190(3.4); 1.182(2.0); 1.167(1.0); 1.159(2.3); 1.152(1.3); 1.129(0.8); 1.066(2.0); 1.059 (2.3); 1.036(4.0); 1.028(5.2); 1.005(3.6); 0.999(3.7); 0.977(1.3); 0.966(1.1); 0.008(1.3); 0.000(38.2); 0.009(1.3) Example II-347: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.571(4.9); 7.577(10.1); 7.575(11.6); 7.573(11.5); 7.571(11.2); 7.521 (0.7); 7.362(10.4); 7.360(10.8); 7.353(10.5); 7.351(10.5); 7.262(124.1); 6.998(0.7); 6.746(2.3); 6.620(10.3); 6.616(10.4); 6.611(10.4); 6.607(10.2); 5.299(1.5); 3.362(10.7); 3.346(16.0); 3.331(10.7); 1.806(4.6); 1.781(9.4); 1.777(9.1); 1.756 (4.5); 1.748(5.2); 1.713(2.4); 1.710(2.5); 1.702(1.7); 1.682(2.3); 1.679(2.3); 1.672(2.0); 1.655(1.1); 1.647(1.4); 1.635(1.7); 1.627(2.3); 1.618(2.8); 1.610(2.2); 1.599(2.0); 1.590(2.3); 1.572(22.6); 1.331(0.7); 1.321(1.1); 1.312(0.8); 1.290(3.4); 1.266 (4.0); 1.258(5.6); 1.226(4.6); 1.201(1.8); 1.194(3.5); 1.186(2.0); 1.171(1.0); 1.163(2.3); 1.156(1.2); 1.133(0.7); 1.072 (2.0); 1.064(2.3); 1.042(4.0); 1.034(5.2); 1.011(3.7); 1.005(3.8); 0.982(1.3); 0.971(1.1); 0.008(1.7); 0.000(49.7); 0.009 (1.8) Example II-348: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.440(4.0); 7.520(0.6); 7.261(113.5); 6.997(0.6); 6.726(2.4); 5.298 (0.7); 3.359(10.9); 3.343(16.0); 3.327(11.2); 1.789(6.5); 1.780(6.6); 1.769(6.9); 1.761(7.7); 1.748(5.6); 1.715(2.4); 1.711 (2.5); 1.707(2.0); 1.703(1.7); 1.684(2.2); 1.654(0.7); 1.645(1.0); 1.637(1.4); 1.625(1.6); 1.617(2.3); 1.608(2.8); 1.600(2.2); 1.591(2.0); 1.588(2.1); 1.573(6.5); 1.328(0.6); 1.317(1.1); 1.309(0.7); 1.286(3.3); 1.262(3.9); 1.255(5.4); 1.223(4.7); 1.198 (1.8); 1.191(3.2); 1.184(2.0); 1.168(1.0); 1.161(2.3); 1.153(1.2); 1.130(0.7); 1.064(2.0); 1.057(2.3); 1.035(4.1); 1.027 (5.0); 1.004(3.5); 0.999(3.6); 0.975(1.3); 0.965(1.0); 0.008(1.3); 0.000(42.0); 0.009(1.2) Example II-349: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.373(3.2); 7.519(2.3); 7.280(0.7); 7.278(0.9); 7.276(1.1); 7.274(1.3); 7.273(1.6); 7.272(1.7); 7.270(2.2); 7.2694(2.4); 7.2686(2.6); 7.260(402.4); 6.996(2.3); 6.710(2.0); 5.298(2.1); 3.362 (11.2); 3.346(16.0); 3.330(11.4); 1.790(6.2); 1.780(6.4); 1.770(6.9); 1.763(7.4); 1.748(5.4); 1.715(2.3); 1.711(2.5); 1.707 (2.0); 1.704(1.6); 1.684(2.2); 1.655(0.8); 1.647(1.1); 1.638(1.4); 1.627(1.6); 1.618(2.3); 1.610(2.8); 1.602(2.2); 1.590(1.9); 1.581(2.0); 1.573(1.9); 1.548(19.1); 1.328(0.6); 1.318(1.1); 1.287(3.3); 1.263(4.0); 1.255(5.7); 1.224(4.6); 1.199(1.8); 1.192 (3.3); 1.184(2.0); 1.169(1.0); 1.161(2.3); 1.153(1.2); 1.130(0.7); 1.066(2.0); 1.059(2.2); 1.036(4.0); 1.028(4.8); 1.006 (3.4); 1.001(3.4); 0.976(1.3); 0.966(1.0); 0.157(0.9); 0.008(4.5); 0.006(1.8); 0.000(156.2); 0.007(1.6); 0.009(4.7) Example II-35: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.591(1.2); 7.519(0.6); 7.432(0.6); 7.411(1.4); 7.395(1.4); 7.390(0.9); 7.374(0.8); 7.260(106.3); 7.069(0.7); 6.996(0.6); 6.908(0.7); 6.905(0.6); 6.901(0.8); 6.899(0.9); 6.887(1.0); 6.879(3.4); 6.874(0.7); 6.866(0.6); 6.859(2.3); 6.855(1.6); 6.849(1.0); 6.833(1.2); 6.827(0.9); 5.298(1.0); 4.670(3.8); 4.654(3.8); 2.597 (1.0); 1.815(0.5); 1.796(2.3); 1.778(4.1); 1.759(4.1); 1.741(2.3); 1.722(0.6); 1.544(22.8); 1.042(7.7); 1.024(16.0); 1.005 (7.0); 0.008(1.2); 0.000(42.4); 0.009(1.1) Example II-350: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.647(2.5); 8.635(2.5); 7.520(1.0); 7.273(0.8); 7.272(0.8); 7.270(1.0); 7.262(170.8); 7.254(1.2); 7.253(0.9); 6.997(0.9); 6.717(2.1); 5.298(0.9); 3.357(11.4); 3.341(16.0); 3.325(11.6); 1.797 (4.7); 1.788(5.1); 1.779(7.4); 1.771(8.7); 1.755(5.1); 1.746(5.0); 1.713(2.4); 1.709(2.5); 1.705(2.0); 1.701(1.7); 1.682(2.2); 1.678(2.2); 1.658(1.0); 1.649(1.1); 1.641(1.4); 1.629(1.6); 1.621(2.3); 1.612(2.9); 1.604(2.2); 1.593(1.8); 1.586(2.9); 1.583 (3.1); 1.575(1.6); 1.568(5.3); 1.566(6.6); 1.562(8.8); 1.558(45.9); 1.548(9.0); 1.546(8.1); 1.541(6.2); 1.539(6.5); 1.537 (5.6); 1.528(4.1); 1.526(4.2); 1.513(3.8); 1.510(4.8); 1.509(5.2); 1.506(2.9); 1.500(5.8); 1.499(6.2); 1.496(5.7); 1.492(4.7); 1.490(4.4); 1.485(2.4); 1.475(1.6); 1.472(2.1); 1.465(4.1); 1.463(4.4); 1.454(5.6); 1.452(5.9); 1.450(5.7); 1.445(5.1); 1.443 (4.4); 1.437(2.9); 1.427(2.0); 1.426(1.9); 1.328(0.7); 1.318(1.2); 1.310(0.7); 1.287(3.3); 1.279(2.3); 1.263(3.8); 1.256 (5.6); 1.224(4.6); 1.199(1.8); 1.192(3.5); 1.184(2.1); 1.169(1.0); 1.161(2.5); 1.154(1.3); 1.130(0.8); 1.067(2.0); 1.059(2.3); 1.037(4.0); 1.029(5.0); 1.006(3.5); 1.000(3.6); 0.977(1.2); 0.967(1.1); 0.008(1.8); 0.000(60.8); 0.007(0.8); 0.009 (1.9) Example II-351: .sup.1H-NMR(400.0 MHz, d.sub.6DMSO): = 10.542(12.1); 8.645(2.3); 8.631(4.4); 8.616(2.3); 8.311(1.4); 3.901 (8.4); 3.508(0.5); 3.448(0.4); 3.430(0.6); 3.406(0.8); 3.391(1.5); 3.379(2.3); 3.371(1.5); 3.329(942.4); 3.294(3.5); 3.272 (1.1); 3.258(0.7); 3.239(0.4); 3.214(0.5); 3.205(0.4); 3.189(0.4); 3.174(0.7); 3.164(0.7); 3.134(8.1); 3.117(12.8); 3.102 (8.1); 2.676(1.9); 2.671(2.6); 2.667(1.9); 2.598(0.3); 2.570(0.5); 2.560(0.8); 2.555(0.9); 2.542(0.6); 2.524(6.5); 2.511(155.4); 2.507(316.3); 2.502(417.7); 2.497(310.6); 2.493(156.9); 2.469(1.8); 2.428(0.4); 2.333(1.7); 2.329(2.3); 2.324(1.7); 1.719 (5.2); 1.691(9.6); 1.673(5.9); 1.628(3.0); 1.609(7.6); 1.595(14.4); 1.587(16.0); 1.575(8.7); 1.567(1.9); 1.557(1.8); 1.547 (2.1); 1.539(2.6); 1.533(2.5); 1.521(1.8); 1.512(1.6); 1.502(1.0); 1.489(1.2); 1.447(7.9); 1.435(14.2); 1.428(13.2); 1.413 (5.4); 1.235(1.3); 1.210(2.8); 1.180(5.2); 1.159(5.5); 1.115(1.4); 1.084(0.5); 0.969(2.2); 0.940(5.0); 0.913(3.8); 0.888 (1.3); 0.878(1.1); 0.863(0.4); 0.008(0.3); 0.000(10.6); 0.008(0.4) Example II-352: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.469(2.3); 7.519(1.2); 7.273(0.8); 7.272(0.8); 7.271(0.9); 7.270(1.0); 7.269(1.5); 7.268(1.7); 7.267(1.9); 7.266(2.2); 7.261(216.7); 7.253(0.7); 6.997(1.2); 6.719(2.0); 5.298(1.3); 3.362(11.3); 3.346(16.0); 3.330(11.6); 1.791(5.9); 1.787(5.9); 1.780(6.3); 1.770(6.9); 1.763(7.4); 1.747(5.4); 1.718(2.1); 1.715(2.4); 1.711(2.6); 1.707(2.1); 1.703(1.9); 1.684(2.3); 1.673(1.6); 1.656(0.7); 1.647(1.0); 1.639(1.3); 1.627(1.6); 1.619(2.2); 1.610 (2.7); 1.602(2.1); 1.593(1.7); 1.590(1.7); 1.582(1.9); 1.573(1.6); 1.556(17.0); 1.328(0.6); 1.318(1.1); 1.310(0.7); 1.287 (3.2); 1.263(3.8); 1.255(5.2); 1.224(4.5); 1.199(1.9); 1.192(3.3); 1.184(2.0); 1.169(1.1); 1.161(2.4); 1.153(1.3); 1.130(0.7); 1.066(2.0); 1.059(2.2); 1.036(3.9); 1.029(4.8); 1.006(3.4); 1.000(3.5); 0.976(1.4); 0.966(1.0); 0.069(0.6); 0.008(2.4); 0.007 (0.8); 0.006(0.8); 0.005(0.9); 0.004(1.2); 0.000(79.0); 0.009(2.0) Example II-353: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.263(45.0); 6.673(0.9); 6.429(4.1); 5.064(0.8); 3.341(3.5); 3.325(5.2); 3.309(3.6); 2.385(16.0); 1.781(2.5); 1.777(2.6); 1.769(1.7); 1.757(2.7); 1.751(3.2); 1.710(0.8); 1.707(0.9); 1.703(0.7); 1.699(0.6); 1.679(0.7); 1.618(0.5); 1.610(0.7); 1.601(0.9); 1.593(0.7); 1.577(5.1); 1.283(1.1); 1.275(0.7); 1.258(1.3); 1.251 (1.6); 1.220(1.5); 1.195(0.6); 1.188(1.0); 1.181(0.6); 1.158(0.7); 1.053(0.7); 1.046(0.8); 1.023(1.3); 1.017(1.7); 0.992 (1.3); 0.008(0.5); 0.000(16.8) Example II-354: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.519(0.6); 7.269(0.7); 7.260(108.6); 7.254(0.6); 6.996(0.6); 6.708 (0.7); 5.299(0.8); 3.358(3.7); 3.342(5.3); 3.326(3.8); 1.872(16.0); 1.854(15.7); 1.794(1.5); 1.787(1.7); 1.778(2.1); 1.770(2.6); 1.764(2.3); 1.754(1.8); 1.745(1.7); 1.713(0.8); 1.709(0.8); 1.706(0.7); 1.701(0.5); 1.682(0.7); 1.627(0.5); 1.618(0.7); 1.610(0.9); 1.601(0.7); 1.593(0.5); 1.590(0.5); 1.581(0.5); 1.543(9.8); 1.286(1.0); 1.262(1.2); 1.254(1.8); 1.223(1.5); 1.198 (0.6); 1.191(1.1); 1.183(0.7); 1.160(0.8); 1.066(0.6); 1.058(0.7); 1.036(1.3); 1.028(1.6); 1.006(1.1); 0.999(1.2); 0.008 (1.2); 0.000(40.4); 0.009(1.2) Example II-355: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.692(1.2); 7.263(35.6); 6.721(0.6); 3.349(3.5); 3.333(4.9); 3.317(3.8); 3.304(0.8); 2.692(0.9); 2.676(0.9); 1.794(1.7); 1.791(1.7); 1.785(1.9); 1.769(2.9); 1.761(2.6); 1.752(1.9); 1.744(1.8); 1.711(0.8); 1.707(0.9); 1.703(0.7); 1.699(0.6); 1.696(0.5); 1.680(0.8); 1.677(0.8); 1.673(0.6); 1.669(0.6); 1.622(0.6); 1.613 (0.8); 1.605(1.0); 1.596(0.9); 1.585(2.2); 1.576(0.9); 1.284(1.2); 1.273(7.6); 1.255(16.0); 1.236(7.0); 1.229(1.2); 1.220 (1.8); 1.197(0.7); 1.190(1.2); 1.182(0.7); 1.159(0.9); 1.062(0.7); 1.054(0.8); 1.032(1.4); 1.024(1.7); 1.001(1.2); 0.996(1.3); 0.000(14.9) Example II-356: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.324(2.4); 7.518(3.9); 7.355(8.0); 7.350(3.7); 7.342(8.4); 7.333(9.7); 7.325(4.1); 7.320(9.3); 7.313(1.5); 7.259(732.6); 7.097(1.5); 7.089(12.0); 7.084(3.6); 7.073(4.0); 7.068(21.1); 7.062 (3.7); 7.051(3.4); 7.046(9.9); 7.038(1.0); 6.995(4.0); 6.922(2.1); 6.248(1.1); 6.112(2.1); 5.978(1.2); 5.298(1.4); 4.651(16.0); 4.637(15.8); 2.004(0.6); 1.536(159.1); 1.255(1.4); 0.146(0.9); 0.069(1.0); 0.008(8.9); 0.000(280.2); 0.009(7.8); 0.150 (0.9) Example II-357: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.603(1.4); 7.348(2.5); 7.343(1.1); 7.335(2.6); 7.326(3.0); 7.318(1.2); 7.313(2.9); 7.260(77.9); 7.081(3.8); 7.075(1.2); 7.064(1.2); 7.059(6.7); 7.054(1.3); 7.043(1.1); 7.037(3.2); 6.946(0.7); 4.639(4.8); 4.625(4.8); 2.617(1.0); 1.755(0.9); 1.737(2.1); 1.731(0.8); 1.718(2.8); 1.699(2.1); 1.694(0.8); 1.680(1.1); 1.550 (8.5); 1.473(0.6); 1.455(1.9); 1.436(2.7); 1.417(2.8); 1.398(1.8); 1.380(0.6); 0.968(7.5); 0.949(16.0); 0.931(6.4); 0.008 (0.9); 0.000(31.2); 0.009(0.9) Example II-358: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.360(1.3); 7.354(0.6); 7.347(1.4); 7.343(0.8); 7.338(1.6); 7.330(0.6); 7.324(1.5); 7.260(20.2); 7.089(2.0); 7.084(0.6); 7.073(0.6); 7.068(3.6); 7.062(0.7); 7.051(0.6); 7.046(1.7); 4.648(2.5); 4.634(2.5); 2.527(1.3); 1.655(0.9); 1.637(2.4); 1.631(0.9); 1.618(3.1); 1.613(1.4); 1.599(2.6); 1.594(0.9); 1.580(1.3); 1.375 (0.6); 1.357(1.9); 1.338(2.6); 1.323(1.0); 1.319(2.7); 1.300(1.8); 1.282(0.6); 0.910(7.6); 0.892(16.0); 0.873(6.3); 0.000 (8.3) Example II-359: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.589(1.1); 7.519(0.6); 7.349(2.3); 7.343(1.1); 7.335(2.5); 7.327(2.8); 7.319(1.1); 7.313(2.7); 7.260(109.8); 7.082(3.6); 7.076(1.1); 7.065(1.1); 7.060(6.3); 7.055(1.2); 7.043(1.0); 7.038(3.0); 6.996(0.6); 6.941(0.6); 4.640(4.4); 4.626(4.4); 2.599(0.9); 1.816(0.5); 1.797(2.3); 1.779(4.1); 1.760(4.0); 1.742(2.2); 1.723 (0.6); 1.543(26.1); 1.043(7.6); 1.024(16.0); 1.006(6.9); 0.008(1.3); 0.000(43.6); 0.009(1.3) Example II-36: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.261(14.9); 3.349(0.5); 3.333(0.7); 3.317(0.5); 1.554(0.9); 1.355(16.0); 1.350(0.6); 0.000(5.7) Example II-360: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.357(1.1); 7.351(0.5); 7.344(1.2); 7.340(0.7); 7.335(1.4); 7.327(0.6); 7.322(1.4); 7.260(28.6); 7.088(1.7); 7.082(0.6); 7.071(0.6); 7.066(3.0); 7.061(0.6); 7.045(1.5); 4.648(2.2); 4.634(2.2); 2.576(1.1); 2.559(1.1); 1.545(4.1); 1.153(7.2); 1.135(16.0); 1.117(6.9); 0.000(11.6) Example II-361: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.624(1.1); 7.349(2.4); 7.343(1.0); 7.336(2.6); 7.327(3.0); 7.319(1.2); 7.314(2.9); 7.260(78.1); 7.081(3.7); 7.076(1.2); 7.065(1.2); 7.060(6.7); 7.054(1.4); 7.043(1.1); 7.038(3.3); 7.030(0.6); 6.942(0.6); 5.298(1.4); 4.640(4.7); 4.625(4.7); 2.682(0.9); 2.666(0.9); 1.551(13.4); 1.268(7.7); 1.249(16.0); 1.231(7.4); 0.008 (0.9); 0.000(30.6); 0.009(0.9) Example II-362: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.361(0.6); 7.348(0.6); 7.339(0.7); 7.326(0.6); 7.261(8.1); 7.089(0.9); 7.068(1.5); 7.046(0.7); 4.651(1.1); 4.637(1.1); 2.298(16.0); 1.558(0.6); 0.000(3.2) Example II-363: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.629(3.0); 7.518(2.3); 7.358(0.9); 7.350(7.8); 7.345(3.3); 7.337(8.2); 7.334(4.8); 7.332(4.7); 7.328(9.5); 7.321(3.8); 7.315(9.2); 7.310(1.1); 7.308(1.1); 7.292(0.7); 7.259(412.4); 7.251(1.3); 7.249(0.9); 7.248(0.8); 7.246(0.5); 7.091(1.3); 7.084(12.0); 7.078(3.7); 7.067(3.8); 7.062(20.8); 7.057(4.0); 7.046(3.3); 7.040(9.9); 7.033(1.0); 6.996(2.4); 6.930(2.0); 5.298(2.9); 4.642(16.0); 4.628(15.8); 2.408(8.7); 1.540(73.4); 1.255(0.6); 0.146(0.5); 0.008(5.3); 0.000(177.8); 0.009(5.0); 0.150(0.6) Example II-364: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.565(2.1); 7.518(3.4); 7.349(3.7); 7.343(1.7); 7.336(3.9); 7.327(4.6); 7.319(1.8); 7.314(4.2); 7.306(0.9); 7.298(0.6); 7.293(0.7); 7.284(1.1); 7.259(611.3); 7.228(0.6); 7.208(0.5); 7.090(0.6); 7.082(5.6); 7.077(1.8); 7.066(1.7); 7.061(9.8); 7.055(1.9); 7.044(1.6); 7.039(4.6); 6.995(3.5); 6.933(1.1); 4.641(7.4); 4.626 (7.3); 2.614(1.6); 1.773(0.7); 1.755(2.2); 1.736(3.1); 1.717(2.4); 1.699(0.9); 1.532(149.0); 1.415(0.5); 1.402(1.1); 1.394 (1.8); 1.390(1.6); 1.382(3.9); 1.372(7.3); 1.363(5.5); 1.354(4.0); 1.348(2.0); 1.331(0.9); 0.928(5.9); 0.925(2.7); 0.920 (2.1); 0.911(16.0); 0.897(2.1); 0.893(4.3); 0.146(0.8); 0.008(8.1); 0.000(260.6); 0.009(7.5); 0.150(0.8) Example II-365: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 13.260(0.9); 13.258(0.5); 8.738(0.8); 7.519(1.2); 7.360(0.9); 7.353 (8.0); 7.347(3.6); 7.340(8.6); 7.331(9.7); 7.323(3.9); 7.318(9.3); 7.311(1.3); 7.260(220.6); 7.093(1.4); 7.085(12.4); 7.080 (3.8); 7.069(4.0); 7.064(21.7); 7.058(4.1); 7.047(3.4); 7.042(10.3); 7.034(1.0); 6.996(1.3); 6.930(2.2); 5.298(2.6); 4.647(16.0); 4.633(15.7); 4.316(7.0); 4.314(6.2); 4.116(0.5); 1.552(18.7); 1.255(1.3); 1.248(1.4); 1.231(0.7); 0.069(0.6); 0.008(2.8); 0.000(85.2); 0.009(2.3) Example II-366: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.436(1.6); 7.519(1.3); 7.354(7.7); 7.349(3.5); 7.341(8.2); 7.332(9.6); 7.325(3.8); 7.319(9.0); 7.312(1.1); 7.260(232.2); 7.094(1.3); 7.086(11.7); 7.081(3.7); 7.070(3.9); 7.065(20.8); 7.060 (4.2); 7.048(3.3); 7.043(9.9); 7.035(1.1); 6.996(1.3); 6.928(2.1); 5.106(4.7); 4.988(4.8); 4.648(16.0); 4.634(15.8); 1.544(29.2); 1.255(0.8); 0.008(2.7); 0.000(92.6); 0.009(2.8) Example II-367: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.257(2.9); 7.518(4.2); 7.355(8.0); 7.350(3.3); 7.342(8.5); 7.333(9.6); 7.326(3.8); 7.320(9.3); 7.293(0.8); 7.259(787.3); 7 227(1.1); 7.098(1.4); 7.091(12.4); 7.085(3.6); 7.074(4.0); 7.069(21.2); 7.064(3.9); 7.053(3.4); 7.047(10.2); 7.040(1.1); 6.995(4.3); 6.926(2.2); 4.653(16.0); 4.639(15.7); 1.537(191.5); 1.256 (0.7); 0.146(0.9); 0.008(8.9); 0.000(299.8); 0.009(8.5); 0.150(0.8) Example II-368: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.451(1.4); 7.519(1.1); 7.374(2.7); 7.360(2.9); 7.355(5.2); 7.340(5.3); 7.335(3.9); 7.320(3.7); 7.273(0.7); 7.271(0.9); 7.269(1.2); 7.260(202.1); 7.253(0.9); 7.252(0.7); 7.251(0.6); 7.2503(0.6); 7.2496(0.5); 7.146(5.6); 7.145(5.7); 7.129(3.3); 7.127(4.6); 7.126(4.8); 7.081(2.5); 7.075(4.0); 7.071(3.0); 7.057(2.5); 7.052(4.1); 7.048(5.4); 7.041(2.0); 7.026(4.4); 7.025(4.4); 7.019(3.4); 7.005(2.6); 7.003(2.7); 6.996(3.6); 6.979(1.9); 5.298 (4.7); 5.110(4.2); 4.992(4.3); 4.681(16.0); 4.667(15.8); 1.547(47.8); 0.069(0.7); 0.008(2.3); 0.000(79.3); 0.009(2.2) Example II-369: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.341(2.7); 7.519(1.1); 7.431(2.7); 7.427(3.0); 7.412(5.6); 7.408(6.1); 7.394(3.2); 7.389(3.3); 7.354(1.8); 7.350(1.5); 7.341(1.9); 7.336(4.0); 7.331(3.0); 7.322(3.5); 7.316(4.5); 7.311(2.8); 7.302 (2.5); 7.297(2.3); 7.260(189.5); 7.174(5.0); 7.171(5.5); 7.155(8.1); 7.152(8.7); 7.136(3.8); 7.133(4.0); 7.125(5.0); 7.100 (7.0); 7.079(6.0); 6.996(1.1); 6.246(1.2); 6.112(2.3); 5.977(1.2); 5.298(1.2); 4.728(16.0); 4.714(15.6); 1.546(50.6); 1.246 (1.1); 0.008(3.2); 0.000(74.6); 0.009(2.5) Example II-370: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.330(2.2); 7.519(0.5); 7.476(3.6); 7.470(2.3); 7.464(4.0); 7.461(2.8); 7.453(4.5); 7.444(0.7); 7.440(0.6); 7.430(4.2); 7.424(3.2); 7.420(3.6); 7.418(2.5); 7.412(3.0); 7.407(6.1); 7.398(0.8); 7.320 (0.8); 7.313(1.9); 7.307(0.9); 7.301(8.3); 7.298(9.0); 7.294(6.3); 7.288(11.8); 7.281(6.7); 7.277(8.1); 7.275(8.7); 7.260 (95.9); 6.996(0.5); 4.758(16.0); 4.743(15.8); 1.569(14.2); 0.008(1.2); 0.000(36.0); 0.009(0.9) Example II-371: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.351(1.7); 7.519(0.7); 7.479(3.6); 7.473(2.2); 7.467(4.5); 7.464(2.9); 7.456(4.5); 7.447(0.5); 7.439(0.5); 7.429(4.2); 7.423(3.1); 7.419(4.2); 7.412(2.8); 7.406(6.1); 7.398(0.8); 7.318(0.6); 7.311 (1.8); 7.306(1.0); 7.299(8.3); 7.297(8.8); 7.293(6.0); 7.287(9.4); 7.286(8.9); 7.280(6.1); 7.275(9.2); 7.260(117.3); 6.996 (0.7); 6.245(0.7); 6.110(1.4); 5.976(0.7); 5.297(0.6); 4.758(16.0); 4.743(15.8); 1.554(15.4); 1.259(0.6); 1.246(0.6); 0.008 (1.3); 0.000(44.8); 0.009(1.3) Example II-372: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.353(2.1); 7.519(0.9); 7.344(8.5); 7.321(8.1); 7.318(10.6); 7.313(5.7); 7.308(16.7); 7.305(17.9); 7.298(1.7); 7.294(1.5); 7.288(1.1); 7.281(0.7); 7.275(1.1); 7.260(171.4); 7.251(4.1); 7.245 (4.3); 7.243(4.9); 7.237(2.3); 7.233(2.2); 7.229(2.1); 6.996(1.6); 6.973(1.8); 6.249(0.9); 6.116(1.8); 5.981(0.9); 5.298(1.0); 4.758(0.8); 4.743(0.8); 4.663(16.0); 4.649(15.8); 1.549(31.9); 1.257(0.5); 0.008(2.2); 0.000(64.7); 0.009(1.7) Example II-373: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.287(2.3); 7.518(1.6); 7.347(6.6); 7.345(7.9); 7.341(4.9); 7.332(0.7); 7.324(8.6); 7.321(12.0); 7.317(5.4); 7.311(14.5); 7.308(17.4); 7.301(1.3); 7.297(1.1); 7.291(0.9); 7.259(272.1); 7.251 (3.9); 7.244(4.3); 7.238(2.0); 7.233(2.1); 7.229(1.9); 6.995(2.2); 6.971(1.7); 5.298(1.6); 4.666(16.0); 4.652(15.7); 1.544 (61.0); 0.008(3.7); 0.000(109.9); 0.009(2.9) Example II-374: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.447(3.8); 8.048(1.7); 7.519(2.3); 7.434(2.4); 7.412(5.7); 7.397(6.1); 7.391(4.1); 7.376(3.6); 7.310(0.8); 7.273(1.5); 7.272(1.6); 7.269(2.5); 7.267(3.3); 7.266(3.8); 7.265(4.5); 7.260(423.8); 7.256(8.0); 7.255(6.0); 7.2533(2.7); 7.2525(1.7); 7.252(1.3); 7.251(1.0); 7.250(0.9); 7.249(1.1); 7.248(0.6); 7.061(2.8); 6.996(2.4); 6.915(2.8); 6.912(2.6); 6.909(3.6); 6.906(4.0); 6.894(4.1); 6.886(14.6); 6.882(3.1); 6.873(2.7); 6.866(9.8); 6.862 (6.5); 6.856(4.2); 6.840(5.0); 6.834(3.8); 6.369(2.3); 6.355(4.8); 6.342(2.3); 6.237(4.8); 6.224(10.2); 6.210(5.0); 6.106 (2.4); 6.092(5.1); 6.079(2.5); 4.680(16.0); 4.666(15.7); 4.638(0.7); 4.624(0.6); 1.550(50.9); 1.254(1.0); 0.008(4.6); 0.006 (1.7); 0.005(2.2); 0.000(154.4); 0.003(7.9); 0.007(1.5); 0.009(4.4) Example II-375: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 9.074(3.2); 9.032(3.1); 8.261(4.2); 8.257(4.5); 8.241(8.5); 8.237(8.4); 8.221(4.4); 8.217(4.2); 7.624(2.3); 7.619(2.6); 7.611(2.7); 7.606(5.4); 7.592(4.0); 7.585(5.9); 7.580(3.2); 7.572(3.3); 7.567 (2.8); 7.518(8.0); 7.449(3.0); 7.428(6.3); 7.412(6.2); 7.390(3.6); 7.377(6.3); 7.375(7.1); 7.356(10.0); 7.339(5.5); 7.336 (6.1); 7.309(7.7); 7.260(1415.0); 7.232(4.4); 7.222(4.8); 7.219(4.7); 7.208(3.8); 7.198(5.1); 7.101(3.3); 6.996(7.7); 6.907 (3.6); 6.895(4.6); 6.887(11.5); 6.861(6.1); 6.854(4.0); 6.839(4.7); 6.832(3.4); 4.689(16.0); 4.675(15.5); 1.538(126.0); 1.254(1.4); 0.331(2.3); 0.238(1.5); 0.157(2.3); 0.146(1.7); 0.050(2.3); 0.008(17.7); 0.000(523.5); 0.009(16.8); 0.150 (1.9) Example II-376: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.358(2.8); 8.061(1.2); 7.518(5.8); 7.437(2.4); 7.417(5.7); 7.401(5.9); 7.395(4.1); 7.379(3.4); 7.359(0.9); 7.322(0.9); 7.288(1.6); 7.285(1.6); 7.268(7.2); 7.260(1065.7); 7.252(6.7); 7.248(1.8); 7.246(1.4); 7.241(0.9); 7.236(0.9); 7.232(0.9); 7.210(1.0); 7.062(2.8); 6.996(5.9); 6.915(2.5); 6.913(2.5); 6.909(3.3); 6.907 (3.4); 6.895(4.1); 6.887(13.1); 6.874(2.7); 6.866(9.4); 6.856(3.9); 6.841(4.7); 6.834(3.5); 6.583(1.6); 6.514(0.8); 6.457 (1.6); 6.387(0.8); 5.299(2.6); 4.682(16.0); 4.667(15.6); 3.242(1.2); 1.546(34.1); 1.257(0.7); 0.146(1.4); 0.008(12.2); 0.000 (412.3); 0.009(12.9); 0.149(1.3) Example II-377: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.893(3.0); 8.857(3.1); 7.990(2.5); 7.986(4.6); 7.981(2.6); 7.974(2.6); 7.969(6.5); 7.965(6.8); 7.961(2.9); 7.954(2.7); 7.949(4.8); 7.945(2.5); 7.764(0.6); 7.519(4.8); 7.466(2.5); 7.462(2.7); 7.446 (6.1); 7.442(6.6); 7.438(3.3); 7.427(8.4); 7.422(7.9); 7.418(5.2); 7.412(6.3); 7.406(4.2); 7.402(3.8); 7.398(3.4); 7.390 (3.6); 7.379(0.6); 7.371(0.5); 7.321(3.7); 7.317(3.9); 7.309(3.6); 7.305(3.9); 7.301(5.9); 7.297(5.8); 7.289(5.9); 7.285(6.4); 7.280(3.9); 7.276(4.1); 7.260(913.7); 7.247(1.5); 7.239(0.6); 7.226(1.0); 7.223(0.6); 7.210(1.0); 7.185(0.7); 7.169(1.0); 7.098(3.2); 6.996(5.0); 6.917(2.8); 6.915(2.6); 6.911(3.5); 6.908(3.7); 6.896(4.3); 6.888(12.8); 6.882(2.7); 6.876(2.5); 6.867 (7.7); 6.863(6.0); 6.856(3.9); 6.841(5.0); 6.835(3.6); 5.298(2.8); 4.691(16.0); 4.676(15.8); 3.245(1.5); 1.540(11.4); 1.427 (0.7); 1.254(1.3); 0.146(1.1); 0.069(2.4); 0.017(0.6); 0.013(0.9); 0.008(10.7); 0.006(3.4); 0.0054(4.1); 0.0046(5.0); 0.000 (349.7); 0.005(5.8); 0.006(4.3); 0.007(3.6); 0.009(10.1); 0.012(1.3); 0.013(1.1); 0.021(0.6); 0.034(0.6); 0.150 (1.1) Example II-379: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.665(1.2); 7.431(0.6); 7.410(1.4); 7.394(1.5); 7.389(1.0); 7.373(0.9); 7.262(36.1); 7.078(0.7); 6.907(0.7); 6.904(0.6); 6.901(0.9); 6.898(1.1); 6.886(1.1); 6.878(3.6); 6.874(0.8); 6.866(0.7); 6.858(2.5); 6.854(1.6); 6.848(1.1); 6.832(1.3); 6.826(1.0); 4.669(4.0); 4.654(4.0); 2.679(1.0); 2.660(1.0); 1.574(6.8); 1.265 (7.7); 1.247(16.0); 1.228(7.4); 0.000(14.3) Example II-380: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.598(2.2); 7.519(0.7); 7.432(0.9); 7.410(2.1); 7.395(2.2); 7.389(1.4); 7.373(1.3); 7.260(127.8); 7.070(1.1); 6.996(0.7); 6.908(1.0); 6.905(0.9); 6.901(1.3); 6.899(1.4); 6.887(1.6); 6.879(5.3); 6.874(1.0); 6.866(1.0); 6.858(3.6); 6.855(2.5); 6.848(1.5); 6.833(1.9); 6.826(1.4); 4.669(5.9); 4.654(5.8); 2.611(1.5); 1.771 (0.7); 1.753(2.1); 1.734(3.0); 1.715(2.3); 1.697(0.9); 1.548(27.1); 1.400(1.0); 1.392(1.8); 1.389(1.5); 1.383(2.6); 1.380 (3.7); 1.371(7.4); 1.362(5.3); 1.359(4.2); 1.353(4.2); 1.347(2.0); 1.341(1.4); 1.330(0.8); 0.928(5.7); 0.924(2.6); 0.919(2.0); 0.910(16.0); 0.905(2.9); 0.897(2.0); 0.892(4.2); 0.008(1.4); 0.000(48.5); 0.009(1.5) Example II-382: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.769(3.5); 8.062(1.2); 7.519(1.1); 7.437(2.5); 7.419(3.1); 7.415(6.0); 7.399(6.2); 7.394(3.7); 7.378(3.4); 7.260(200.7); 7.082(2.8); 6.996(1.1); 6.915(2.7); 6.912(2.5); 6.908(3.5); 6.906(3.8); 6.894(4.3); 6.886(13.1); 6.880(2.8); 6.873(2.6); 6.865(7.9); 6.860(6.3); 6.854(4.1); 6.838(4.9); 6.832(3.7); 5.298(3.7); 4.684 (16.0); 4.669(15.8); 2.610(0.6); 1.558(10.6); 1.248(0.6); 0.008(2.1); 0.000(71.7); 0.009(2.1) Example II-384: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.577(6.0); 7.519(4.8); 7.432(2.5); 7.410(5.9); 7.394(6.0); 7.388(3.8); 7.373(3.7); 7.359(1.2); 7.311(3.9); 7.292(3.6); 7.260(902.3); 7.230(1.2); 7.159(1.5); 7.140(1.4); 7.071(3.3); 6.996(4.8); 6.904(2.6); 6.898(3.7); 6.886(4.4); 6.878(12.7); 6.873(2.8); 6.866(2.6); 6.857(8.3); 6.847(3.8); 6.831(4.5); 6.825(3.4); 5.298 (7.1); 4.669(16.0); 4.654(15.6); 2.529(1.4); 2.002(5.3); 1.969(5.8); 1.858(5.2); 1.826(6.7); 1.728(3.4); 1.698(2.6); 1.592 (3.1); 1.561(8.1); 1.540(143.9); 1.509(3.3); 1.392(1.8); 1.383(2.1); 1.361(3.9); 1.353(5.3); 1.322(7.0); 1.299(7.0); 1.279 (4.2); 1.271(2.8); 1.249(3.1); 1.219(1.1); 0.331(1.5); 0.238(1.1); 0.157(1.5); 0.146(1.3); 0.127(1.0); 0.051(1.3); 0.033 (1.0); 0.008(10.3); 0.000(330.7); 0.008(12.3); 0.150(1.2) Example II-385: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.811(0.8); 7.411(0.9); 7.395(0.9); 7.390(0.6); 7.261(43.1); 7.069(0.6); 6.900(0.5); 6.887(0.7); 6.880(2.0); 6.859(1.4); 6.850(0.6); 6.834(0.7); 4.669(2.5); 4.654(2.5); 3.697(0.8); 3.689(16.0); 3.668(14.6); 2.712(0.7); 2.491(1.9); 2.485(2.0); 2.473(4.1); 2.467(4.3); 2.454(2.2); 2.449(2.3); 2.355(1.8); 2.336(3.9); 2.318 (2.1); 2.096(0.5); 2.079(2.0); 2.061(2.8); 2.043(1.7); 1.930(0.5); 1.912(1.9); 1.894(2.7); 1.876(1.7); 1.558(4.7); 0.008 (0.6); 0.000(16.1); 0.008(0.6) Example II-386: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.262(10.0); 6.889(0.8); 4.676(1.0); 4.661(1.0); 3.681(16.0); 2.657 (1.1); 2.641(1.8); 2.625(0.8); 1.564(2.0); 0.000(4.1) Example II-387: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.605(1.5); 7.432(0.6); 7.410(1.5); 7.395(1.6); 7.389(1.0); 7.373(0.9); 7.260(73.1); 7.072(0.8); 6.907(0.7); 6.905(0.7); 6.901(0.9); 6.899(1.0); 6.887(1.1); 6.879(3.6); 6.874(0.7); 6.866(0.7); 6.858(2.5); 6.848(1.1); 6.833(1.3); 6.826(0.9); 5.298(2.4); 4.669(4.3); 4.654(4.2); 2.618(1.1); 1.754(0.9); 1.736(2.2); 1.731 (0.9); 1.717(2.9); 1.698(2.2); 1.679(1.1); 1.552(16.6); 1.472(0.6); 1.454(1.9); 1.435(2.9); 1.416(3.0); 1.398(1.9); 1.379 (0.6); 0.967(7.7); 0.949(16.0); 0.930(6.5); 0.008(0.9); 0.000(28.0); 0.009(0.8) Example II-388: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.346(4.2); 7.518(5.0); 7.431(2.3); 7.411(5.7); 7.396(5.7); 7.390(3.9); 7.374(3.3); 7.259(917.7); 7.208(1.5); 7.066(3.2); 6.995(5.1); 6.914(2.6); 6.906(3.4); 6.893(4.3); 6.886(12.7); 6.873(2.5); 6.866(9.0); 6.856(3.7); 6.840(4.4); 6.834(3.3); 4.680(16.0); 4.665(15.8); 1.538(47.4); 0.157(2.1); 0.146(1.2); 0.008(12.0); 0.000(335.7); 0.009(11.2); 0.149(1.3) Example II-389: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.343(5.0); 8.052(0.7); 7.518(2.2); 7.432(2.3); 7.410(5.6); 7.395(5.9); 7.389(3.9); 7.373(3.5); 7.293(0.7); 7.259(418.5); 7.210(0.7); 7.073(3.1); 6.995(2.3); 6.914(2.6); 6.912(2.5); 6.908(3.5); 6.905(3.7); 6.893(4.1); 6.885(13.9); 6.881(3.1); 6.873(2.5); 6.865(9.5); 6.862(6.7); 6.855(4.1); 6.840(4.8); 6.833(3.7); 4.680 (16.0); 4.665(15.7); 4.638(0.5); 1.543(27.5); 1.254(0.7); 0.156(0.9); 0.008(4.7); 0.006(1.9); 0.000(157.2); 0.008(4.8) Example II-390: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.463(4.8); 8.053(0.5); 7.519(1.1); 7.431(2.3); 7.409(5.6); 7.394(5.8); 7.388(3.8); 7.372(3.3); 7.260(192.4); 7.079(2.9); 6.996(1.1); 6.913(2.7); 6.911(2.6); 6.907(3.5); 6.905(3.8); 6.892(4.4); 6.884(13.9); 6.880(2.9); 6.872(2.6); 6.864(9.6); 6.860(6.4); 6.854(4.1); 6.839(4.8); 6.832(3.6); 5.298(11.1); 4.679(16.0); 4.665(15.8); 4.571(0.9); 4.556(0.9); 3.963(8.6); 1.563(7.1); 1.255(0.7); 0.008(1.9); 0.000(69.8); 0.009(2.0) Example II-391: .sup.1H-NMR(400.0 MHz, d.sub.6-DMSO): = 10.560(13.2); 9.230(3.2); 9.216(6.2); 9.203(3.6); 8.313(0.4); 7.489 (2.2); 7.468(5.1); 7.450(5.1); 7.429(2.5); 7.273(2.7); 7.268(3.1); 7.243(5.5); 7.224(2.9); 7.218(3.2); 7.109(3.1); 7.093 (5.4); 7.088(5.6); 7.072(3.0); 7.066(2.9); 4.494(13.3); 4.480(14.2); 4.022(0.4); 3.901(2.2); 3.509(0.5); 3.390(4.8); 3.327(198.8); 3.170(0.6); 2.672(1.5); 2.502(280.5); 2.355(0.6); 2.329(2.0); 2.182(0.4); 2.124(0.5); 1.610(4.8); 1.596(13.2); 1.588 (16.0); 1.577(8.0); 1.534(1.1); 1.491(1.1); 1.448(7.0); 1.437(15.1); 1.429(15.0); 1.416(5.7); 1.378(0.6); 1.334(0.5); 1.318 (0.5); 1.309(0.4); 1.299(0.6); 1.260(0.7); 1.235(1.9); 1.185(1.0); 1.167(1.3); 0.872(0.5); 0.854(0.7); 0.001(5.3); 0.000(5.9) Example II-392: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.818(0.5); 7.435(0.6); 7.418(0.8); 7.414(1.5); 7.398(1.5); 7.393(0.9); 7.377(0.8); 7.261(67.5); 7.067(0.8); 6.911(0.7); 6.908(0.7); 6.905(0.9); 6.902(1.0); 6.890(1.1); 6.882(3.3); 6.877(0.6); 6.870(0.7); 6.861(2.2); 6.857(1.5); 6.851(1.0); 6.835(1.2); 6.829(0.9); 4.677(4.6); 4.662(4.5); 1.863(16.0); 1.846(15.9); 1.548 (2.9); 0.008(0.8); 0.000(25.6); 0.009(0.7) Example II-393: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.460(1.5); 7.520(0.7); 7.273(0.7); 7.272(0.7); 7.271(0.8); 7.270(0.9); 7.2693(1.0); 7.2685(1.1); 7.261(129.6); 7.028(2.0); 6.997(1.1); 6.914(0.6); 6.908(1.2); 6.902(1.1); 6.896(5.7); 6.892 (6.6); 6.891(7.7); 6.881(3.7); 6.877(7.2); 6.875(6.7); 6.872(5.1); 6.871(6.1); 6.865(1.0); 6.859(1.1); 6.794(1.7); 6.788(2.9); 6.782(1.4); 6.772(3.5); 6.766(5.8); 6.760(2.7); 6.750(1.8); 6.744(2.9); 6.738(1.3); 5.114(4.7); 4.996(4.7); 4.666(16.0); 4.651 (15.8); 1.554(22.6); 1.255(0.6); 1.248(0.6); 0.008(1.6); 0.006(0.6); 0.005(0.6); 0.000(51.6); 0.009(1.4) Example II-394: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.355(2.3); 7.519(1.1); 7.260(199.5); 7.019(2.0); 6.996(1.8); 6.913 (0.6); 6.908(1.3); 6.896(5.8); 6.890(7.9); 6.876(7.3); 6.875(6.9); 6.871(6.2); 6.859(1.1); 6.797(1.8); 6.791(3.0); 6.786(1.5); 6.775(3.6); 6.769(6.0); 6.763(2.8); 6.753(1.9); 6.747(3.0); 6.741(1.4); 6.254(1.1); 6.120(2.1); 5.985(1.1); 4.668(16.0); 4.653 (15.7); 1.549(21.6); 1.246(1.0); 0.008(2.4); 0.000(76.4); 0.009(2.1) Example II-395: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.463(3.1); 8.330(1.2); 7.260(61.6); 7.029(0.9); 6.996(0.5); 6.907(0.5); 6.895(2.4); 6.889(3.3); 6.876(3.1); 6.870(2.6); 6.799(0.7); 6.793(1.2); 6.788(0.6); 6.777(1.5); 6.771(2.4); 6.765(1.1); 6.755(0.8); 6.749(1.2); 6.743(0.6); 4.670(6.7); 4.655(6.6); 3.963(16.0); 1.566(3.2); 0.008(0.9); 0.000(23.5); 0.009(0.6) Example II-396: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.753(0.8); 7.519(1.9); 7.309(0.7); 7.260(362.5); 7.013(2.0); 6.996 (3.3); 6.908(1.3); 6.896(6.0); 6.890(8.1); 6.876(7.6); 6.871(6.3); 6.859(1.2); 6.853(0.6); 6.795(1.9); 6.789(3.1); 6.783(1.5); 6.773(3.6); 6.767(6.0); 6.761(2.9); 6.751(1.8); 6.745(3.0); 6.739(1.4); 5.298(4.8); 4.668(16.0); 4.653(15.7); 4.327(6.0); 4.114(0.5); 1.540(71.5); 1.255(1.5); 1.243(1.3); 0.008(4.5); 0.000(135.8); 0.009(3.7); 0.150(0.5) Example II-397: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.262(16.3); 6.896(0.9); 6.890(1.2); 6.876(1.1); 6.871(0.9); 6.766(0.5); 6.761(0.9); 4.663(2.5); 4.648(2.4); 4.116(4.2); 3.544(16.0); 1.562(2.2); 0.000(6.5) Example II-398: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.276(2.9); 7.518(2.8); 7.291(0.8); 7.259(495.6); 7.235(0.6); 7.226 (0.5); 7.214(3.0); 7.209(3.1); 7.202(3.6); 7.195(3.1); 7.189(4.0); 7.181(9.4); 7.177(3.8); 7.168(3.1); 7.162(7.3); 7.156(6.5); 7.137(5.2); 7.109(2.6); 7.106(3.2); 7.099(3.8); 7.095(3.4); 7.090(3.0); 7.079(2.1); 7.074(1.9); 6.995(4.1); 6.978(2.2); 5.298 (2.8); 4.639(16.0); 4.624(15.7); 4.603(0.9); 1.542(111.3); 1.255(1.0); 0.146(0.6); 0.008(5.5); 0.000(181.8); 0.009 (5.3); 0.150(0.6) Example II-399: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.342(2.6); 7.519(1.7); 7.292(0.5); 7.260(312.5); 7.250(0.7); 7.248 (0.6); 7.213(2.9); 7.207(3.2); 7.200(3.6); 7.194(3.1); 7.188(3.9); 7.179(8.3); 7.175(3.6); 7.167(3.1); 7.159(5.9); 7.154(6.1); 7.134(5.1); 7.105(3.2); 7.098(3.7); 7.094(3.4); 7.089(2.9); 7.084(2.2); 7.078(2.0); 7.073(1.9); 7.062(0.7); 6.996(3.0); 6.978 (2.3); 6.250(1.2); 6.115(2.3); 5.982(1.2); 5.298(8.8); 4.637(16.0); 4.622(15.8); 2.306(0.9); 1.543(32.0); 1.256(0.8); 0.008 (3.6); 0.000(119.7); 0.009(3.4) Example II-400: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.337(2.9); 7.519(2.4); 7.260(431.2); 7.227(0.8); 7.209(0.8); 7.160 (0.9); 7.145(3.0); 7.137(3.7); 7.131(3.5); 7.124(6.2); 7.116(4.6); 7.110(4.8); 7.102(5.2); 7.091(5.1); 7.080(4.7); 7.069(8.4); 7.058(8.1); 7.046(5.7); 7.035(5.6); 7.027(3.3); 7.019(3.1); 7.017(3.7); 7.008(5.4); 7.005(2.1); 6.998(4.6); 6.996(4.7); 6.990 (2.9); 6.986(2.7); 6.978(1.7); 6.968(1.3); 6.251(1.3); 6.116(2.5); 5.981(1.2); 5.298(1.9); 4.697(16.0); 4.681(15.8); 1.541 (98.1); 1.255(0.7); 0.146(0.5); 0.008(5.2); 0.000(160.1); 0.009(4.2); 0.150(0.5) Example II-401: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.322(3.6); 7.519(1.1); 7.310(0.7); 7.260(190.2); 7.142(3.4); 7.134 (4.3); 7.127(4.6); 7.120(7.5); 7.113(5.8); 7.107(5.6); 7.099(5.2); 7.093(4.4); 7.081(3.6); 7.070(8.0); 7.059(8.0); 7.047(5.7); 7.036(5.6); 7.029(3.4); 7.021(3.1); 7.018(3.8); 7.010(5.4); 7.006(2.2); 7.002(3.3); 6.999(4.6); 6.996(3.0); 6.992(3.0); 6.988 (2.8); 6.979(1.7); 6.977(1.7); 6.969(1.3); 5.298(0.9); 4.697(16.0); 4.682(15.8); 1.566(15.0); 0.008(2.4); 0.000(71.9); 0.009 (1.9) Example II-402: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.452(1.8); 7.520(1.0); 7.311(0.8); 7.261(169.6); 7.145(2.9); 7.138 (3.5); 7.131(3.4); 7.124(6.1); 7.117(4.8); 7.110(4.6); 7.103(5.4); 7.088(4.3); 7.077(3.7); 7.065(7.5); 7.054(7.5); 7.043(5.4); 7.032(5.1); 7.023(2.9); 7.015(2.8); 7.013(3.4); 7.004(4.9); 7.000(2.1); 6.996(3.9); 6.994(4.2); 6.986(2.9); 6.982(2.6); 6.974 (1.6); 6.971(1.7); 6.964(1.3); 5.298(1.0); 5.110(5.4); 4.992(5.4); 4.747(0.6); 4.694(15.2); 4.679(16.0); 4.663(1.3); 1.553 (30.6); 1.255(0.5); 0.008(2.1); 0.000(66.9); 0.009(1.9) Example II-403: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.748(0.9); 7.519(1.9); 7.288(0.8); 7.285(1.0); 7.282(1.0); 7.260(374.3); 7.145(3.1); 7.137(3.6); 7.130(3.6); 7.123(6.2); 7.116(4.7); 7.110(4.8); 7.102(5.4); 7.088(4.9); 7.077(4.6); 7.066(8.1); 7.054(8.1); 7.043(5.7); 7.032(5.5); 7.024(3.1); 7.016(3.2); 7.013(3.7); 7.005(5.2); 7.001(2.3); 6.996(5.3); 6.987(3.0); 6.982 (2.6); 6.974(1.7); 6.964(1.3); 5.298(4.3); 4.695(15.9); 4.680(16.0); 4.324(7.0); 4.115(0.8); 1.545(51.2); 1.247(2.3); 0.008 (4.5); 0.000(138.9); 0.009(4.2); 0.150(0.5) Example II-404: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.300(0.9); 7.279(0.6); 7.261(34.2); 6.960(1.3); 6.940(1.6); 6.920(1.1); 4.785(1.9); 4.770(1.9); 4.107(3.2); 3.535(16.0); 1.553(2.2); 0.000(12.4) Example II-405: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.436(1.6); 7.520(1.2); 7.343(2.0); 7.327(4.1); 7.322(3.6); 7.310(2.4); 7.306(8.2); 7.301(2.8); 7.289(4.0); 7.285(5.1); 7.268(4.2); 7.261(213.5); 7.078(2.5); 6.997(1.3); 6.979(1.2); 6.975(1.7); 6.965(10.9); 6.957(1.7); 6.954(2.2); 6.945(13.6); 6.936(2.3); 6.932(1.9); 6.925(9.8); 6.914(1.6); 6.911(1.1); 5.105(4.6); 4.986(4.5); 4.789(16.0); 4.774(15.8); 4.754(0.7); 1.553(30.6); 1.242(1.2); 0.008(2.6); 0.000(82.7); 0.009(2.4) Example II-406: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.732(0.8); 7.519(1.6); 7.343(1.9); 7.326(4.0); 7.322(3.6); 7.310(2.4); 7.305(8.1); 7.301(2.9); 7.289(3.6); 7.284(5.0); 7.268(4.2); 7.260(290.0); 7.078(2.6); 6.996(1.6); 6.978(1.1); 6.974(1.7); 6.964(11.0); 6.957(1.7); 6.953(2.0); 6.945(13.9); 6.935(2.2); 6.931(1.6); 6.924(9.9); 6.914(1.5); 6.910(1.1); 5.298(9.8); 4.789(16.0); 4.774(15.8); 4.316(6.0); 1.548(42.5); 1.255(0.6); 0.008(3.2); 0.000(108.7); 0.009(3.2) Example II-407: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.290(2.9); 7.519(1.4); 7.348(2.0); 7.332(4.0); 7.327(3.6); 7.316(2.4); 7.311(8.0); 7.306(2.8); 7.294(3.7); 7.290(5.2); 7.273(3.5); 7.260(247.9); 7.087(2.5); 6.996(1.5); 6.982(1.2); 6.978(1.7); 6.968(11.1); 6.960(1.7); 6.957(1.9); 6.948(13.8); 6.939(2.0); 6.935(1.6); 6.928(9.7); 6.918(1.3); 6.914(1.0); 4.793(16.0); 4.779(15.7); 1.553(22.7); 1.255(0.6); 0.008(3.1); 0.000(96.0); 0.009(2.8) Example II-408: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.327(2.6); 7.519(2.5); 7.346(2.0); 7.330(3.9); 7.325(3.8); 7.314(2.3); 7.309(8.2); 7.304(2.8); 7.292(3.8); 7.288(5.4); 7.271(3.8); 7.260(460.8); 7.075(2.5); 6.996(2.5); 6.981(1.2); 6.977(1.7); 6.967(10.9); 6.960(1.5); 6.956(1.8); 6.948(13.6); 6.938(2.0); 6.934(1.7); 6.927(9.8); 6.917(1.4); 6.244(1.0); 6.110(2.0); 5.973(1.0); 4.792(16.0); 4.778(15.8); 1.541(104.4); 1.256(0.8); 0.146(0.6); 0.008(5.1); 0.000(171.7); 0.009(4.7) Example II-409: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.340(3.1); 7.519(2.3); 7.352(0.5); 7.260(423.1); 7.227(0.7); 7.210 (0.9); 7.199(2.8); 7.188(3.9); 7.183(6.1); 7.180(5.7); 7.166(7.6); 7.164(7.1); 7.148(5.0); 7.142(5.5); 7.138(3.3); 7.124(5.1); 7.119(8.2); 7.116(6.5); 7.107(7.4); 7.104(7.1); 7.101(5.7); 7.098(7.3); 7.095(5.4); 7.089(5.4); 7.086(6.4); 7.080(3.4); 7.077 (3.0); 7.068(1.9); 7.065(2.0); 6.996(2.3); 6.250(1.3); 6.115(2.7); 5.981(1.4); 4.752(16.0); 4.738(15.8); 1.542(117.8); 0.146 (0.5); 0.008(5.1); 0.000(160.4); 0.009(4.6); 0.149(0.6) Example II-410: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.897(0.7); 7.260(63.5); 7.156(1.0); 7.144(1.0); 7.133(1.2); 7.120(1.4); 7.111(1.1); 7.098(0.9); 6.910(0.6); 6.888(0.9); 4.796(3.3); 4.781(3.2); 4.110(5.7); 3.538(16.0); 1.540(11.2); 0.000(24.0) Example II-411: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.745(1.0); 7.518(5.8); 7.288(1.3); 7.259(1058.3); 7.210(1.0); 7.184 (1.8); 7.172(1.8); 7.161(5.0); 7.148(5.0); 7.139(5.3); 7.126(6.2); 7.115(4.3); 7.103(4.6); 6.995(5.7); 6.923(2.2); 6.918(2.7); 6.914(2.6); 6.909(2.5); 6.901(3.4); 6.892(3.8); 6.886(3.5); 6.878(2.2); 6.873(2.3); 6.869(2.2); 6.864(1.9); 5.298(8.9); 4.800 (16.0); 4.786(15.8); 4.321(6.7); 1.534(265.8); 0.146(1.1); 0.069(0.9); 0.008(12.2); 0.000(394.8); 0.009(11.4); 0.149 (1.4) Example II-412: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.263(3.2); 7.518(3.1); 7.311(0.7); 7.290(0.5); 7.288(0.7); 7.275(1.6); 7.273(1.7); 7.271(2.2); 7.268(3.7); 7.266(5.3); 7.260(555.3); 7.250(1.7); 7.249(1.5); 7.247(1.1); 7.228(0.8); 7.190(1.9); 7.177(2.1); 7.167(5.1); 7.154(5.3); 7.144(5.5); 7.132(6.3); 7.121(4.2); 7.108(4.4); 6.996(3.1); 6.928(2.4); 6.923(2.6); 6.919 (2.6); 6.914(2.6); 6.906(3.3); 6.900(3.7); 6.897(3.7); 6.891(3.4); 6.883(2.1); 6.878(2.2); 6.874(2.2); 6.869(1.9); 5.298 (0.8); 4.806(16.0); 4.791(15.7); 1.540(128.4); 1.256(0.9); 0.146(0.6); 0.008(6.6); 0.006(2.6); 0.000(210.6); 0.009(5.8); 0.150 (0.7) Example II-413: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.436(1.9); 7.519(3.3); 7.260(578.2); 7.184(1.9); 7.172(2.0); 7.162 (5.0); 7.149(5.3); 7.139(5.5); 7.126(6.4); 7.116(4.4); 7.103(4.3); 6.996(3.0); 6.924(2.3); 6.918(2.5); 6.915(2.7); 6.909(2.5); 6.902(3.4); 6.896(3.8); 6.887(3.4); 6.879(2.1); 6.874(2.1); 6.870(2.1); 6.864(2.0); 5.107(5.4); 4.989(5.4); 4.801(16.0); 4.786 (15.9); 2.004(0.6); 1.538(100.3); 1.256(0.7); 0.146(0.8); 0.008(6.8); 0.000(217.5); 0.009(6.5); 0.150(0.7) Example II-414: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.339(3.1); 7.519(1.1); 7.260(189.3); 7.187(1.7); 7.174(1.9); 7.164 (4.7); 7.151(4.9); 7.141(5.4); 7.129(6.4); 7.118(4.5); 7.106(4.3); 6.996(1.1); 6.926(2.2); 6.920(2.6); 6.917(2.4); 6.911(2.4); 6.904(3.5); 6.898(3.9); 6.889(3.3); 6.881(1.9); 6.875(2.1); 6.872(1.9); 6.866(1.7); 6.247(1.3); 6.112(2.5); 5.977(1.4); 5.298 (0.8); 4.802(16.0); 4.788(15.6); 4.115(0.7); 3.642(0.6); 1.548(36.7); 1.256(2.0); 0.000(70.3); 0.008(2.8) Example II-415: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.573(1.2); 7.518(1.0); 7.260(189.1); 7.047(0.7); 6.996(1.1); 6.747 (0.6); 6.738(2.6); 6.719(3.6); 6.717(3.6); 6.698(2.6); 6.689(0.5); 5.298(1.0); 4.720(3.8); 4.705(3.7); 2.598(1.0); 1.813(0.5); 1.794(2.3); 1.776(4.2); 1.757(4.1); 1.739(2.3); 1.720(0.6); 1.543(8.3); 1.041(7.7); 1.022(16.0); 1.004(6.9); 0.008(2.2); 0.000 (77.1); 0.009(2.2) Example II-416: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.569(1.4); 7.518(1.0); 7.259(189.4); 7.043(0.8); 6.996(1.0); 6.746 (0.5); 6.738(2.7); 6.719(3.7); 6.717(3.8); 6.698(2.7); 6.689(0.5); 5.298(0.6); 4.720(4.0); 4.705(4.0); 2.621(1.1); 1.753(0.9); 1.735(2.1); 1.729(0.9); 1.715(2.8); 1.696(2.1); 1.677(1.1); 1.537(34.9); 1.471(0.6); 1.453(1.9); 1.434(2.8); 1.415(2.9); 1.397 (1.8); 1.378(0.6); 0.967(7.5); 0.948(16.0); 0.930(6.5); 0.008(2.2); 0.000(78.6); 0.009(2.2) Example II-417: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.260(34.9); 7.112(0.8); 6.747(2.0); 6.733(0.5); 6.728(2.7); 6.725(2.8); 6.720(0.5); 6.706(2.0); 4.733(2.9); 4.719(2.9); 2.514(1.7); 1.669(0.8); 1.651(2.4); 1.643(1.2); 1.632(3.4); 1.625(1.4); 1.614(2.4); 1.595(0.8); 1.545(4.1); 1.323(0.7); 1.305(1.8); 1.300(4.3); 1.293(4.6); 1.291(5.3); 1.282(7.0); 1.273(3.8); 1.264 (1.5); 1.261(1.6); 1.253(0.8); 0.894(4.7); 0.877(16.0); 0.867(1.7); 0.859(4.4); 0.000(14.6) Example II-418: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.570(2.1); 7.518(1.4); 7.259(257.7); 7.045(1.2); 6.995(1.5); 6.746 (0.8); 6.738(3.9); 6.725(1.0); 6.719(5.2); 6.717(5.4); 6.711(1.0); 6.697(3.8); 6.689(0.7); 4.720(5.9); 4.705(5.8); 2.613(1.5); 1.770(0.7); 1.751(2.2); 1.732(3.0); 1.713(2.3); 1.695(0.8); 1.537(41.8); 1.399(1.0); 1.391(1.8); 1.388(1.6); 1.382(2.7); 1.379(3.7); 1.370(7.5); 1.361(5.2); 1.358(4.3); 1.352(4.2); 1.346(2.0); 1.340(1.4); 1.328(0.8); 0.927(5.7); 0.923(2.6); 0.918 (2.1); 0.910(16.0); 0.904(2.9); 0.896(2.0); 0.892(4.2); 0.008(3.3); 0.000(111.5); 0.009(3.1) Example II-419: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.260(27.5); 6.745(1.2); 6.726(1.6); 6.724(1.7); 6.705(1.2); 4.731(1.7); 4.716(1.7); 2.568(1.1); 2.551(1.1); 1.552(1.8); 1.150(7.1); 1.132(16.0); 1.114(6.9); 0.000(10.6) Example II-420: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.603(1.1); 7.519(0.7); 7.260(130.9); 7.042(0.7); 6.996(0.8); 6.747 (0.6); 6.739(2.8); 6.725(0.8); 6.719(3.8); 6.717(3.9); 6.712(1.2); 6.698(2.7); 6.690(0.8); 4.720(4.3); 4.706(4.5); 4.693(0.7); 2.685(1.0); 2.668(1.0); 1.542(22.7); 1.265(7.8); 1.247(16.0); 1.228(7.4); 0.008(1.6); 0.000(54.2); 0.009(1.4) Example II-421: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.633(3.8); 7.519(2.2); 7.292(1.2); 7.286(0.6); 7.260(401.5); 7.037 (2.6); 6.996(2.5); 6.757(1.1); 6.749(2.0); 6.740(10.2); 6.727(2.6); 6.721(13.9); 6.719(14.1); 6.713(2.6); 6.700(9.9); 6.692 (1.9); 6.683(0.9); 5.298(5.9); 4.722(16.0); 4.707(15.8); 2.404(11.3); 2.004(0.9); 1.544(79.4); 1.255(0.7); 0.146(0.5); 0.032 (0.5); 0.008(5.2); 0.000(173.1); 0.009(4.8); 0.150(0.5) Example II-422: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.261(9.3); 6.747(0.6); 6.728(0.8); 6.726(0.8); 6.707(0.6); 4.735(0.9); 4.720(0.9); 2.292(16.0); 1.550(1.3); 0.000(3.8) Example II-423: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.432(2.1); 7.519(2.6); 7.260(461.2); 7.034(3.0); 6.996(2.9); 6.761 (0.9); 6.752(2.2); 6.744(10.0); 6.724(14.3); 6.722(14.5); 6.703(10.1); 6.695(2.4); 6.686(1.2); 5.298(1.7); 5.106(5.9); 4.987 (5.8); 4.729(15.9); 4.714(16.0); 4.635(0.5); 1.537(95.8); 1.255(1.3); 0.146(0.6); 0.008(5.5); 0.000(168.6); 0.009(6.9); 0.150 (0.6) Example II-424: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.888(0.6); 7.261(25.2); 7.037(0.7); 6.738(1.6); 6.717(2.5); 6.698(1.5); 4.724(2.9); 4.709(2.9); 4.108(5.3); 3.537(16.0); 1.548(7.2); 0.000(9.1) Example II-425: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.721(1.1); 7.519(1.6); 7.260(282.7); 7.210(1.1); 7.036(3.2); 6.996 (2.0); 6.760(1.1); 6.751(2.2); 6.743(9.8); 6.723(14.3); 6.721(14.1); 6.702(10.0); 6.694(2.3); 6.685(1.3); 5.298(0.6); 4.729 (15.9); 4.714(16.0); 4.319(7.7); 1.541(48.3); 1.255(0.9); 0.008(4.2); 0.000(108.4); 0.009(4.6) Example II-426: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.325(2.9); 7.519(1.9); 7.260(345.9); 7.035(2.7); 6.996(2.1); 6.762 (1.1); 6.754(2.1); 6.745(10.4); 6.732(2.8); 6.726(14.3); 6.724(14.4); 6.718(2.6); 6.705(10.2); 6.697(2.0); 6.688(0.9); 6.246 (1.2); 6.111(2.4); 5.976(1.2); 5.298(0.9); 4.731(16.0); 4.717(15.6); 1.541(79.0); 1.255(0.7); 0.008(4.1); 0.000(132.3); 0.009 (3.8) Example II-427: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.258(3.0); 7.518(2.6); 7.292(0.8); 7.260(475.7); 7.210(1.0); 7.042 (2.6); 6.996(2.7); 6.764(1.1); 6.755(2.0); 6.747(10.7); 6.734(2.7); 6.728(14.4); 6.726(14.6); 6.720(2.6); 6.707(10.5); 6.698 (2.0); 6.690(1.2); 5.298(2.3); 4.734(16.0); 4.719(15.6); 4.691(0.5); 1.542(43.5); 1.255(3.1); 1.232(0.9); 0.880(0.5); 0.008 (5.3); 0.000(184.3); 0.009(5.1); 0.149(0.5) Example II-428: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.281(4.2); 7.519(1.3); 7.260(240.0); 7.197(2.4); 7.190(2.6); 7.176 (4.5); 7.156(4.8); 7.150(3.0); 7.142(2.8); 7.136(2.7); 7.089(3.6); 7.019(3.1); 7.013(3.0); 7.001(3.5); 6.996(7.5); 6.990(3.9); 6.978(4.1); 6.973(5.5); 6.968(2.6); 6.956(2.3); 6.950(2.2); 4.705(16.0); 4.690(15.7); 1.550(37.9); 1.257(0.7); 0.008(4.9); 0.000(90.3); 0.009(3.9) Example II-429: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.333(3.5); 7.519(2.1); 7.260(391.1); 7.198(2.2); 7.192(2.2); 7.184 (2.3); 7.178(4.0); 7.170(3.2); 7.157(4.5); 7.151(2.7); 7.143(2.4); 7.137(2.3); 7.085(3.2); 7.017(2.9); 7.012(3.0); 7.000(3.3); 6.994(6.5); 6.988(3.9); 6.976(4.1); 6.971(5.6); 6.966(2.6); 6.954(2.4); 6.948(2.2); 6.250(1.6); 6.115(3.2); 5.981(1.6); 4.703 (15.9); 4.688(16.0); 1.540(79.5); 1.256(0.9); 0.008(5.3); 0.000(146.8); 0.009(5.7) Example II-430: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.338(3.2); 7.519(3.7); 7.310(1.3); 7.288(1.5); 7.260(694.6); 7.197 (0.7); 7.111(3.1); 6.996(3.8); 6.963(1.9); 6.951(5.0); 6.943(7.2); 6.938(4.6); 6.930(5.6); 6.923(6.2); 6.919(5.8); 6.908(3.6); 6.904(3.0); 6.899(3.8); 6.892(1.9); 6.884(2.6); 6.876(1.8); 6.254(1.6); 6.119(2.9); 5.983(1.5); 5.298(1.3); 4.731(15.9); 4.728 (16.0); 4.715(15.7); 4.712(15.7); 3.642(1.1); 2.004(0.6); 1.538(145.9); 1.256(1.5); 0.146(0.8); 0.008(7.9); 0.000(268.4); 0.009(7.5); 0.150(0.9) Example II-431: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.347(2.7); 7.519(1.3); 7.422(5.6); 7.416(5.9); 7.404(5.6); 7.399(5.7); 7.260(224.2); 7.248(3.3); 7.242(3.1); 7.238(4.3); 7.233(4.1); 7.227(4.1); 7.221(3.8); 7.166(9.5); 7.144(14.5); 7.123(6.1); 6.996(2.7); 6.982(2.3); 6.251(1.2); 6.116(2.3); 5.982(1.1); 4.632(16.0); 4.617(15.6); 1.547(46.3); 1.246(1.1); 0.008(3.0); 0.000(82.6); 0.009(2.4) Example II-432: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.306(3.1); 7.519(1.0); 7.421(5.3); 7.416(5.6); 7.404(5.3); 7.399(5.5); 7.260(178.2); 7.253(3.2); 7.248(3.0); 7.242(2.9); 7.238(4.3); 7.232(4.1); 7.226(4.1); 7.221(3.8); 7.167(9.6); 7.145(14.7); 7.124(6.2); 6.996(2.7); 6.988(2.2); 4.633(16.0); 4.618(15.7); 1.563(8.8); 0.008(2.2); 0.000(70.4); 0.009(2.0) Example II-433: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.333(1.9); 7.519(1.5); 7.442(11.0); 7.436(11.6); 7.429(7.9); 7.408 (10.1); 7.281(8.1); 7.276(8.0); 7.271(1.7); 7.260(281.8); 7.221(2.0); 7.211(1.7); 6.996(1.5); 6.247(0.8); 6.112(1.6); 5.980 (0.8); 5.298(0.6); 4.716(16.0); 4.700(15.8); 4.100(0.5); 1.542(45.5); 1.246(1.4); 0.008(3.4); 0.000(104.0); 0.009(2.8) Example II-434: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.441(1.4); 7.519(1.3); 7.440(10.9); 7.434(11.9); 7.430(8.2); 7.409 (10.0); 7.279(8.2); 7.274(8.3); 7.260(231.3); 7.254(8.1); 7.232(1.6); 7.220(2.3); 7.210(1.8); 7.205(1.2); 7.160(0.6); 6.996 (1.3); 5.108(3.8); 4.989(3.9); 4.714(16.0); 4.699(15.7); 1.542(36.9); 1.255(0.9); 0.008(3.1); 0.000(87.9); 0.009(2.8) Example II-435: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 13.260(2.1); 8.739(0.6); 8.597(0.7); 7.528(0.6); 7.519(2.3); 7.450(1.6); 7.444(2.2); 7.439(11.8); 7.434(12.5); 7.428(8.9); 7.417(1.8); 7.408(10.1); 7.310(0.5); 7.287(1.5); 7.279(9.0); 7.273(8.8); 7.260(404.9); 7.253(8.1); 7.247(1.7); 7.241(1.6); 7.219(2.4); 7.209(1.8); 6.996(2.1); 5.298(1.8); 4.805(7.0); 4.750(0.6); 4.723(2.6); 4.714(15.9); 4.698(16.0); 4.682(1.1); 4.534(0.9); 4.517(1.1); 4.317(8.4); 4.315(7.7); 1.542(35.4); 1.255(1.6); 0.008(4.9); 0.000(153.4); 0.009(4.0) Example II-436: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.264(1.9); 7.518(2.3); 7.444(10.5); 7.439(11.6); 7.429(7.8); 7.418 (1.2); 7.409(9.8); 7.297(0.6); 7.283(8.4); 7.278(8.3); 7.260(412.9); 7.242(1.7); 7.228(2.4); 7.210(1.6); 6.996(2.3); 4.718(16.0); 4.710(2.2); 4.702(15.7); 4.115(1.2); 4.097(1.2); 3.067(0.7); 3.055(0.6); 1.641(0.6); 1.541(66.0); 1.255(3.2); 1.246(3.3); 1.230(1.7); 0.146(0.5); 0.008(4.9); 0.000(164.4); 0.009(5.0); 0.150(0.6) Example II-437: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.649(1.1); 7.519(0.7); 7.260(137.3); 6.996(0.7); 6.761(0.6); 3.357 (3.5); 3.341(4.9); 3.325(3.5); 2.702(1.0); 2.683(1.0); 1.807(1.3); 1.781(2.8); 1.755(1.2); 1.748(1.5); 1.710(0.7); 1.683(0.7); 1.620(0.7); 1.611(0.8); 1.603(0.7); 1.592(0.5); 1.583(0.6); 1.544(16.3); 1.288(1.1); 1.277(7.5); 1.258(16.0); 1.240(7.0); 1.233(1.0); 1.224(1.4); 1.199(0.6); 1.192(1.1); 1.184(0.7); 1.162(0.7); 1.072(0.6); 1.064(0.7); 1.034(1.5); 1.005(1.1); 0.008 (1.5); 0.000(55.7); 0.009(1.6) Example II-438: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.334(2.8); 7.519(1.2); 7.260(222.7); 7.252(0.6); 6.996(1.2); 6.754 (1.9); 3.369(11.2); 3.353(16.0); 3.337(11.4); 1.805(4.5); 1.795(4.6); 1.779(8.6); 1.761(4.7); 1.753(4.9); 1.719(2.3); 1.715 (2.4); 1.712(1.9); 1.708(1.6); 1.688(2.2); 1.685(2.2); 1.681(1.7); 1.676(1.7); 1.667(1.1); 1.658(1.1); 1.650(1.4); 1.638(1.6); 1.630(2.2); 1.621(2.8); 1.613(2.1); 1.601(1.7); 1.593(1.7); 1.584(1.2); 1.576(0.9); 1.567(0.6); 1.546(24.4); 1.334(0.7); 1.324 (1.1); 1.316(0.7); 1.293(3.3); 1.285(2.3); 1.269(3.8); 1.261(5.6); 1.237(2.5); 1.230(4.2); 1.225(3.9); 1.218(2.1); 1.203 (1.8); 1.196(3.6); 1.188(2.1); 1.172(1.0); 1.165(2.5); 1.157(1.2); 1.134(0.8); 1.077(2.0); 1.070(2.2); 1.047(3.9); 1.039(4.9); 1.016(3.5); 1.010(3.5); 0.987(1.2); 0.977(1.1); 0.008(2.7); 0.000(96.7); 0.009(2.9) Example II-439: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.398(2.2); 7.519(1.2); 7.260(219.4); 6.996(1.1); 6.749(1.9); 6.260 (0.9); 6.124(1.7); 5.989(0.9); 5.298(1.1); 3.366(11.5); 3.350(16.0); 3.334(11.6); 1.805(4.5); 1.793(4.4); 1.784(8.5); 1.779 (8.6); 1.761(4.4); 1.752(4.9); 1.718(2.3); 1.714(2.4); 1.706(1.6); 1.687(2.2); 1.683(2.2); 1.675(1.7); 1.665(1.0); 1.656(1.1); 1.648(1.4); 1.637(1.6); 1.628(2.2); 1.620(2.8); 1.611(2.1); 1.600(1.6); 1.591(1.7); 1.583(1.2); 1.574(0.8); 1.565(0.6); 1.546 (31.8); 1.333(0.7); 1.323(1.1); 1.315(0.7); 1.292(3.2); 1.268(3.9); 1.260(5.5); 1.237(2.4); 1.229(4.2); 1.225(3.9); 1.218 (2.1); 1.203(1.8); 1.195(3.6); 1.188(2.1); 1.172(1.0); 1.165(2.5); 1.157(1.2); 1.134(0.8); 1.076(2.0); 1.069(2.2); 1.046(3.9); 1.038(4.9); 1.015(3.5); 1.009(3.5); 0.986(1.2); 0.976(1.0); 0.008(2.6); 0.000(89.9); 0.009(2.5) Example II-5: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.837(9.3); 7.819(10.2); 7.565(2.3); 7.547(5.8); 7.529(4.0); 7.519(6.2); 7.460(7.0); 7.440(10.5); 7.422(4.9); 7.389(2.1); 7.369(5.2); 7.351(5.7); 7.335(7.5); 7.317(10.5); 7.309(3.2); 7.299(4.7); 7.260(1009.7); 7.226(11.7); 7.210(8.8); 7.123(3.6); 6.996(5.5); 4.104(2.0); 4.095(2.3); 4.086(5.5); 4.078(5.8); 4.069(5.7); 4.060(5.5); 4.051(2.1); 4.043(1.9); 3.914(3.8); 3.898(7.8); 3.893(6.3); 3.881(4.4); 3.877(11.1); 3.860(5.2); 3.811(5.2); 3.794 (10.9); 3.790(4.3); 3.777(6.4); 3.773(7.3); 3.756(3.8); 3.740(4.4); 3.732(4.0); 3.725(4.3); 3.717(4.1); 3.706(5.4); 3.697 (5.1); 3.691(5.1); 3.682(4.8); 3.421(5.4); 3.408(5.8); 3.404(5.2); 3.390(5.3); 3.386(4.7); 3.373(4.4); 3.369(4.5); 3.356 (4.1); 2.065(1.5); 2.049(4.9); 2.031(5.9); 2.018(3.6); 2.001(4.4); 1.985(3.4); 1.966(0.9); 1.952(5.8); 1.936(11.5); 1.916(16.0); 1.899(13.0); 1.882(3.8); 1.645(2.4); 1.626(4.8); 1.614(2.4); 1.605(4.2); 1.595(4.9); 1.587(2.3); 1.575(4.4); 1.557(2.7); 1.542(113.7); 1.333(1.0); 1.284(1.5); 1.255(1.6); 0.146(1.1); 0.008(10.3); 0.000(356.2); 0.009(9.2); 0.150(1.1) Example II-50: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.446(1.4); 7.520(1.0); 7.261(185.6); 7.255(1.1); 7.253(0.8); 6.997(1.0); 6.701(2.0); 5.116(3.7); 4.999(3.7); 3.358(11.0); 3.342(16.0); 3.326(11.2); 1.795(4.8); 1.789(5.5); 1.781(6.4); 1.773(8.0); 1.765(7.4); 1.756(5.6); 1.748(5.1); 1.714(2.4); 1.711(2.5); 1.703(1.7); 1.683(2.3); 1.680(2.2); 1.673(1.6); 1.658(0.8); 1.649(1.0); 1.641(1.4); 1.629(1.6); 1.621(2.3); 1.612(2.8); 1.604(2.2); 1.593(1.7); 1.584(1.9); 1.575(1.5); 1.554(8.4); 1.329 (0.6); 1.319(1.1); 1.311(0.7); 1.288(3.2); 1.264(3.8); 1.256(5.4); 1.225(4.7); 1.200(1.8); 1.193(3.4); 1.185(2.0); 1.170 (1.0); 1.162(2.4); 1.154(1.2); 1.131(0.7); 1.067(2.0); 1.059(2.2); 1.037(4.0); 1.029(5.0); 1.006(3.5); 1.000(3.6); 0.977(1.3); 0.967(1.0); 0.008(2.0); 0.000(64.4); 0.009(1.9) Example II-55: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.444(1.5); 7.519(1.1); 7.433(2.6); 7.429(2.9); 7.414(5.6); 7.410(6.1); 7.395(3.1); 7.391(3.3); 7.351(1.7); 7.347(1.6); 7.338(1.8); 7.333(3.7); 7.328(2.6); 7.317(3.1); 7.312(4.5); 7.307(2.3); 7.298 (2.8); 7.294(2.4); 7.260(193.3); 7.172(5.0); 7.169(5.6); 7.161(0.9); 7.158(1.0); 7.153(8.2); 7.150(9.3); 7.143(1.2); 7.140 (1.2); 7.134(3.8); 7.131(4.1); 7.123(5.0); 7.120(4.5); 7.112(1.2); 7.102(5.0); 7.098(6.5); 7.095(5.7); 7.084(2.8); 7.077(5.3); 7.074(5.0); 6.996(1.1); 5.298(3.2); 5.106(4.4); 4.988(4.4); 4.727(15.4); 4.712(16.0); 4.695(1.5); 1.552(18.3); 1.255(1.2); 1.249(1.1); 1.231(0.6); 0.008(2.3); 0.000(78.5); 0.009(2.3) Example II-56: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.519(1.2); 7.437(2.2); 7.415(5.3); 7.399(5.4); 7.394(3.5); 7.378(3.1); 7.260(228.5); 7.2524(0.7); 7.2516(0.5); 7.026(2.1); 6.996(1.8); 6.902(2.4); 6.899(2.2); 6.895(3.1); 6.893(3.4); 6.881(4.0); 6.873(12.3); 6.860(2.2); 6.852(8.6); 6.842(3.6); 6.827(4.4); 6.820(3.2); 5.298(0.7); 4.736(7.1); 4.660(16.0); 4.645(15.7); 1.550(37.4); 0.008(2.6); 0.000(88.0); 0.009(2.5) Example II-57: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.737(0.7); 7.519(2.8); 7.310(0.7); 7.288(0.8); 7.260(523.7); 7.251(1.5); 7.248(0.9); 7.226(1.2); 6.996(2.9); 6.696(2.0); 5.298(4.4); 4.332(4.6); 3.359(10.9); 3.343(16.0); 3.327(11.0); 1.789(5.7); 1.780(6.4); 1.772(8.1); 1.765(7.5); 1.747(5.1); 1.711(2.5); 1.683(2.3); 1.649(1.0); 1.640(1.4); 1.629(1.6); 1.620(2.1); 1.612(2.7); 1.603(2.2); 1.594(1.7); 1.583(1.7); 1.575(1.2); 1.566(1.0); 1.537(67.3); 1.432(1.1); 1.414(2.2); 1.396(1.0); 1.328 (0.7); 1.319(1.3); 1.287(3.2); 1.263(3.7); 1.256(5.2); 1.224(4.6); 1.199(1.8); 1.192(3.3); 1.185(1.9); 1.162(2.4); 1.154 (1.2); 1.131(0.7); 1.067(2.0); 1.060(2.2); 1.037(4.1); 1.029(5.0); 1.007(3.5); 1.000(3.6); 0.977(1.3); 0.967(1.0); 0.146(0.7); 0.008(6.3); 0.000(207.8); 0.009(5.7); 0.150(0.6) Example II-62: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.743(0.8); 7.519(1.4); 7.431(2.7); 7.427(3.0); 7.412(5.8); 7.408(6.3); 7.393(3.2); 7.389(3.4); 7.351(1.9); 7.347(1.8); 7.338(2.0); 7.332(4.2); 7.328(3.0); 7.318(3.2); 7.312(4.6); 7.307(2.7); 7.298 (2.8); 7.294(2.6); 7.260(245.0); 7.253(1.0); 7.252(0.8); 7.251(0.6); 7.250(0.6); 7.249(0.5); 7.171(5.5); 7.168(6.2); 7.152 (9.1); 7.150(10.1); 7.134(4.2); 7.131(4.4); 7.122(5.2); 7.120(4.6); 7.102(5.4); 7.097(7.1); 7.094(6.2); 7.076(6.0); 7.073 (5.5); 6.996(1.3); 5.298(4.6); 4.726(16.0); 4.711(15.7); 4.322(6.0); 1.546(36.1); 1.255(0.8); 0.008(3.1); 0.000(96.0); 0.009 (2.7) Example II-63: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.746(0.9); 8.070(0.5); 7.520(1.2); 7.437(2.3); 7.415(5.6); 7.399(5.7); 7.394(3.6); 7.378(3.2); 7.276(0.7); 7.275(0.8); 7.274(0.8); 7.273(0.8); 7.272(1.0); 7.2712(1.1); 7.2705(1.3); 7.270(1.6); 7.269(1.8); 7.268(1.9); 7.267(2.3); 7.266(2.8); 7.261(217.6); 7.254(1.1); 7.252(0.6); 7.061(2.8); 6.997(1.3); 6.913(2.5); 6.910 (2.4); 6.906(3.2); 6.904(3.6); 6.891(4.1); 6.884(12.9); 6.879(2.5); 6.871(2.4); 6.863(8.8); 6.859(6.1); 6.853(3.8); 6.837 (4.6); 6.831(3.3); 5.298(1.4); 4.677(16.0); 4.662(15.8); 4.321(7.0); 4.207(1.4); 1.553(8.4); 1.255(1.0); 1.248(0.9); 0.008 (2.7); 0.006(1.3); 0.000(82.5); 0.008(2.2) Example II-64: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.519(2.2); 7.260(397.0); 7.230(0.6); 7.227(0.5); 6.996(2.2); 6.695(2.1); 5.299(0.9); 4.186(3.1); 4.115(0.6); 4.064(2.1); 3.931(0.8); 3.358(10.6); 3.342(16.0); 3.326(10.9); 2.005(0.7); 1.788(6.0); 1.780(6.5); 1.772(8.2); 1.764(7.7); 1.756(6.0); 1.747(5.3); 1.711(2.6); 1.702(1.8); 1.683(2.4); 1.656(0.9); 1.647(1.2); 1.639(1.5); 1.627(1.8); 1.619(2.4); 1.611(2.9); 1.602(2.4); 1.591(2.0); 1.582(2.2); 1.574(2.0); 1.546(13.9); 1.328(0.7); 1.318 (1.2); 1.287(3.3); 1.263(4.3); 1.255(6.1); 1.224(5.0); 1.199(1.8); 1.192(3.4); 1.184(2.0); 1.169(1.1); 1.161(2.4); 1.154 (1.3); 1.130(0.8); 1.066(2.1); 1.059(2.3); 1.036(4.1); 1.029(5.1); 1.006(3.6); 1.000(3.7); 0.976(1.3); 0.966(1.1); 0.008(4.4); 0.000(146.2); 0.009(4.4) Example II-70: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.557(0.7); 7.518(4.0); 7.436(2.2); 7.415(5.3); 7.399(5.5); 7.393(3.5); 7.378(3.2); 7.372(0.9); 7.308(0.9); 7.290(1.0); 7.287(1.2); 7.260(715.4); 7.243(0.9); 7.235(0.7); 7.227(0.8); 7.209(1.1); 7.198(0.6); 7.051(2.8); 6.995(3.9); 6.913(2.3); 6.910(2.4); 6.906(3.1); 6.904(3.4); 6.891(4.0); 6.884(12.5); 6.871(2.4); 6.863 (8.7); 6.853(3.7); 6.838(4.3); 6.832(3.3); 4.677(16.0); 4.662(15.9); 4.176(4.6); 4.054(0.6); 1.538(51.6); 1.255(1.5); 0.146 (0.9); 0.008(8.7); 0.000(272.9); 0.009(8.2); 0.051(0.6); 0.150(0.9) Example II-71: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.263(8.0); 4.277(2.9); 3.411(16.0); 3.368(0.7); 3.352(1.1); 3.336(0.9); 1.776(0.6); 1.769(0.5); 0.000(3.1) Example II-77: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.417(0.7); 7.401(0.7); 7.261(40.4); 6.889(0.5); 6.881(1.5); 6.860(0.9); 6.856(0.7); 6.834(0.5); 4.674(2.0); 4.660(2.1); 4.111(3.8); 3.539(16.0); 1.545(5.4); 0.000(16.0) Example II-78: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.262(20.6); 3.479(1.2); 3.357(1.9); 3.340(2.8); 3.325(1.9); 2.242(16.0); 1.795(0.8); 1.787(0.9); 1.778(1.2); 1.770(1.5); 1.754(0.9); 1.745(0.9); 1.564(0.7); 1.286(0.6); 1.262(0.7); 1.254(1.0); 1.222(0.8); 1.191(0.6); 1.036(0.7); 1.029(0.9); 1.006(0.6); 1.000(0.6); 0.000(7.7) Example II-8: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.311(2.2); 7.306(0.7); 7.295(0.7); 7.289(2.4); 7.260(27.7); 6.901(2.9); 6.896(0.9); 6.885(0.8); 6.880(2.6); 4.558(2.1); 4.544(2.0); 3.809(16.0); 3.329(1.5); 3.313(2.1); 3.297(1.5); 1.786(0.6); 1.776 (0.6); 1.765(1.1); 1.761(1.2); 1.743(0.7); 1.734(0.7); 1.561(1.6); 1.253(1.4); 1.245(0.8); 1.213(0.7); 1.021(0.5); 1.013 (0.7); 0.000(10.5) Example II-84: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.415(0.9); 7.400(0.9); 7.394(0.6); 7.261(26.3); 6.904(0.6); 6.902(0.6); 6.889(0.7); 6.881(1.8); 6.861(1.2); 6.856(0.9); 6.850(0.6); 6.834(0.7); 4.676(2.4); 4.661(2.3); 3.469(1.5); 2.231(16.0); 1.551(0.8); 0.000(10.1) Example II-85: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.264(16.3); 5.300(1.8); 4.014(16.0); 3.358(1.8); 3.342(2.7); 3.326(1.8); 1.795(0.9); 1.790(1.0); 1.781(1.1); 1.773(1.5); 1.765(1.4); 1.756(1.0); 1.748(0.9); 1.577(0.7); 1.288(0.6); 1.264(0.6); 1.257(0.9); 1.225(0.8); 1.193(0.6); 1.037(0.7); 1.029(0.9); 1.006(0.6); 1.000(0.7); 0.000(5.9) Example II-9: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.859(0.6); 7.836(6.7); 7.817(7.7); 7.800(1.2); 7.796(1.0); 7.587(6.6); 7.570(8.4); 7.566(7.7); 7.544(3.7); 7.526(2.7); 7.519(2.1); 7.505(0.8); 7.502(0.6); 7.498(1.5); 7.495(2.9); 7.491(2.0); 7.484 (2.5); 7.477(9.0); 7.470(3.6); 7.462(7.8); 7.459(14.4); 7.455(8.5); 7.444(5.6); 7.440(16.0); 7.438(23.0); 7.435(11.3); 7.424 (10.6); 7.420(18.1); 7.419(14.6); 7.415(5.2); 7.407(3.3); 7.403(6.6); 7.399(4.3); 7.388(1.3); 7.369(3.4); 7.351(4.0); 7.335 (5.2); 7.316(7.2); 7.299(3.1); 7.283(0.6); 7.276(0.6); 7.274(0.7); 7.2723(0.9); 7.2715(0.9); 7.271(1.1); 7.270(1.2); 7.269 (1.3); 7.2682(1.4); 7.2675(1.6); 7.267(1.8); 7.265(2.7); 7.260(213.4); 7.230(8.2); 7.212(7.1); 7.190(2.5); 7.173(0.9); 6.996 (1.2); 4.013(2.5); 4.009(2.5); 3.991(1.4); 3.986(2.5); 3.982(3.0); 3.976(2.2); 3.744(2.8); 3.736(2.9); 3.727(2.8); 3.719 (3.0); 3.710(3.1); 3.702(3.3); 3.693(3.0); 3.685(3.3); 3.514(1.2); 3.508(1.5); 3.500(1.3); 3.493(1.6); 3.486(3.1); 3.481(3.9); 3.472(3.0); 3.466(2.3); 3.458(3.1); 3.453(3.4); 3.446(3.2); 3.427(1.6); 3.417(1.9); 3.250(3.5); 3.239(3.7); 3.230(3.0); 3.219 (3.4); 3.216(3.5); 3.205(3.0); 3.196(2.8); 3.185(2.7); 1.877(2.3); 1.854(1.9); 1.625(2.6); 1.598(3.2); 1.592(3.6); 1.585 (2.1); 1.575(1.2); 1.560(2.8); 1.551(4.8); 1.536(7.2); 1.531(7.0); 1.525(5.2); 1.515(2.5); 1.502(1.7); 1.492(2.2); 1.483(1.2); 1.472(0.8); 1.462(0.9); 1.452(0.6); 1.386(1.4); 1.375(0.9); 1.355(2.4); 1.345(1.7); 1.327(2.2); 1.317(1.4); 1.296(1.2); 1.286 (0.8); 1.259(1.1); 0.882(1.1); 0.008(2.4); 0.006(0.7); 0.000(85.3); 0.007(0.8); 0.009(2.4) Example II-91: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.519(0.5); 7.418(0.7); 7.402(0.7); 7.260(87.8); 6.996(0.5); 6.893(0.5); 6.885(1.7); 6.865(1.2); 6.840(0.6); 4.679(2.1); 4.664(2.1); 4.011(16.0); 1.537(9.3); 0.008(1.1); 0.000(33.4); 0.009 (0.9) Example II-92: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.264(45.2); 6.721(1.0); 5.299(4.0); 3.992(1.9); 3.827(16.0); 3.648(1.2); 3.354(4.8); 3.338(7.3); 3.322(4.9); 1.795(2.2); 1.786(2.3); 1.777(3.4); 1.770(4.0); 1.753(2.3); 1.744(2.3); 1.712(1.1); 1.708(1.1); 1.700(0.7); 1.697(0.7); 1.681(1.0); 1.678(1.0); 1.670(0.7); 1.639(0.6); 1.627(0.7); 1.619(1.0); 1.610(1.3); 1.602 (1.0); 1.590(1.0); 1.579(2.9); 1.565(0.5); 1.317(0.5); 1.286(1.5); 1.278(1.1); 1.262(1.7); 1.254(2.5); 1.223(2.1); 1.198 (0.8); 1.191(1.5); 1.183(0.9); 1.160(1.1); 1.152(0.5); 1.066(0.9); 1.058(1.0); 1.036(1.8); 1.028(2.3); 1.005(1.6); 0.999(1.6); 0.976(0.6); 0.000(15.9) Example II-98: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.436(1.0); 7.415(2.4); 7.399(2.5); 7.394(1.6); 7.378(1.4); 7.261(89.6); 7.076(1.1); 6.997(0.6); 6.909(0.8); 6.907(0.8); 6.900(1.4); 6.888(1.4); 6.880(4.7); 6.873(1.7); 6.868(1.0); 6.859(3.1); 6.855 (2.3); 6.849(1.9); 6.833(1.6); 6.827(1.5); 4.737(0.7); 4.675(5.5); 4.660(6.9); 4.645(1.6); 3.823(16.0); 3.636(1.4); 1.553 (15.1); 0.008(1.1); 0.000(35.0); 0.009(1.0) Example II-99: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.263(19.2); 3.726(0.8); 3.721(16.0); 3.693(0.8); 3.679(0.5); 3.349(1.7); 3.333(2.4); 3.317(1.7); 2.787(1.5); 2.774(1.1); 2.770(1.7); 2.754(1.1); 1.791(0.8); 1.786(0.9); 1.777(1.0); 1.770(1.2); 1.762(1.1); 1.753(0.9); 1.745(0.8); 1.604(0.6); 1.596(0.6); 1.588(0.5); 1.261(0.6); 1.253(0.8); 1.222(0.7); 1.190(0.5); 1.032 (0.6); 1.024(0.7); 1.002(0.5); 0.996(0.5); 0.000(7.5) Example III-19: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.519(0.6); 7.270(0.6); 7.268(0.8); 7.260(106.2); 7.254(0.6); 6.996 (0.6); 6.345(0.5); 6.327(0.5); 4.818(0.9); 4.125(0.7); 4.108(1.0); 4.103(0.8); 4.093(0.8); 4.088(0.9); 4.071(0.7); 1.850(0.8); 1.810(1.7); 1.799(1.2); 1.774(2.1); 1.768(2.3); 1.738(0.8); 1.703(0.9); 1.699(0.7); 1.672(0.9); 1.498(0.7); 1.490(0.9); 1.483 (0.8); 1.476(0.9); 1.468(0.7); 1.461(0.6); 1.454(0.5); 1.447(0.5); 1.284(0.9); 1.277(1.3); 1.269(1.4); 1.256(2.3); 1.245 (1.8); 1.238(1.9); 1.230(16.0); 1.222(1.1); 1.213(15.9); 1.195(0.9); 1.188(0.6); 1.172(0.6); 1.165(1.3); 1.157(0.9); 1.150(0.7); 1.142(0.5); 1.134(1.1); 1.127(1.2); 1.121(1.0); 1.106(0.7); 1.098(1.0); 1.083(1.1); 1.076(1.1); 1.053(0.9); 1.046(0.9); 0.008(1.2); 0.000(40.7); 0.009(1.2) Example III-32: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.260(75.7); 5.769(0.6); 4.862(1.4); 4.044(0.9); 4.027(1.3); 4.021(1.0); 4.011(1.0); 4.005(1.3); 3.989(0.8); 1.790(2.1); 1.783(2.4); 1.761(2.8); 1.716(1.0); 1.694(1.8); 1.689(1.7); 1.685(1.7); 1.666 (1.1); 1.579(0.6); 1.428(0.7); 1.421(1.0); 1.413(1.0); 1.406(1.0); 1.399(0.8); 1.392(0.7); 1.384(0.6); 1.376(0.6); 1.300 (0.6); 1.290(1.0); 1.282(1.1); 1.261(3.3); 1.237(1.3); 1.229(1.9); 1.219(1.6); 1.205(0.9); 1.188(16.0); 1.171(15.0); 1.155 (1.5); 1.147(1.0); 1.132(0.6); 1.124(1.0); 1.116(0.6); 1.099(0.6); 1.092(0.8); 1.069(1.1); 1.060(1.2); 1.039(1.1); 1.031(1.5); 1.009(1.2); 1.002(1.2); 0.979(1.0); 0.971(0.9); 0.899(1.2); 0.882(3.6); 0.864(1.5); 0.008(1.1); 0.000(28.9); 0.008(1.0) Example III-42: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.260(85.1); 6.996(0.6); 3.864(0.6); 3.674(2.6); 3.660(2.7); 3.657(2.8); 3.643(2.7); 2.145(0.8); 2.128(1.0); 2.112(0.8); 1.604(0.7); 1.255(0.9); 1.074(16.0); 1.057(15.4); 0.008(1.1); 0.000(32.9); 0.009(1.0) Example III-43: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.260(83.7); 3.814(0.9); 3.800(1.4); 3.785(1.0); 3.779(1.5); 3.765(2.2); 3.750(1.5); 3.663(1.5); 3.650(1.6); 3.645(1.6); 3.632(1.6); 3.628(1.1); 3.615(1.0); 3.611(1.1); 3.597(1.0); 1.933(0.7); 1.916 (1.1); 1.899(1.1); 1.883(0.8); 1.541(0.8); 1.527(0.9); 1.522(0.9); 1.507(1.4); 1.493(1.0); 1.488(1.2); 1.474(1.0); 1.469 (0.5); 1.364(1.1); 1.345(1.7); 1.327(1.3); 1.311(1.2); 1.292(0.9); 1.256(1.1); 1.057(16.0); 1.040(15.5); 0.994(7.0); 0.975 (15.3); 0.957(5.8); 0.008(1.0); 0.000(32.5); 0.009(1.2) Example III-46: .sup.1H-NMR(300.2 MHz, d.sub.6-DMSO): = 10.350(1.7); 10.322(1.7); 6.487(9.2); 5.759(7.8); 4.438(1.0); 4.414 (1.7); 4.387(1.7); 4.363(1.0); 3.848(1.5); 3.326(20.7); 2.513(3.4); 2.507(7.2); 2.501(9.8); 2.495(7.3); 2.489(3.6); 1.731 (3.8); 1.692(2.9); 1.622(1.8); 1.604(2.1); 1.594(2.2); 1.583(1.8); 1.568(1.6); 1.557(1.2); 1.532(0.7); 1.230(0.8); 1.186(1.9); 1.163(16.0); 1.141(15.4); 1.071(1.7); 1.031(2.7); 0.993(2.0); 0.962(0.7); 0.000(6.3) Example III-52: .sup.1H-NMR(300.2 MHz, d.sub.6-DMSO): = 10.444(1.9); 10.417(1.9); 7.488(1.7); 7.467(3.8); 7.445(1.8); 4.436 (1.0); 4.412(1.8); 4.385(1.8); 4.361(1.1); 4.138(0.9); 4.106(2.8); 4.084(2.9); 4.074(3.1); 4.052(2.8); 4.020(1.0); 3.328 (26.3); 2.513(3.9); 2.508(8.2); 2.502(11.1); 2.496(8.3); 2.490(4.1); 1.778(2.3); 1.733(4.8); 1.694(3.2); 1.627(2.1); 1.602(2.3); 1.593(2.3); 1.568(1.7); 1.544(0.8); 1.530(0.7); 1.355(1.7); 1.237(1.9); 1.168(16.0); 1.146(15.9); 1.076(1.9); 1.035(2.9); 0.998(2.1); 0.967(0.8); 0.878(0.5); 0.858(1.2); 0.836(0.6); 0.000(3.9) Example III-62: .sup.1H-NMR(300.2 MHz, CDCl.sub.3): = 8.255(0.9); 8.233(0.8); 7.263(13.8); 7.005(0.5); 6.999(0.4); 6.993(0.5); 6.976(0.3); 4.969(2.3); 4.669(0.9); 4.647(1.3); 4.640(1.1); 4.627(1.2); 4.620(1.3); 4.598(1.0); 3.878(1.0); 3.866(2.5); 2.796 (0.4); 2.791(0.5); 2.784(0.8); 2.779(1.0); 2.773(1.2); 2.768(1.3); 2.762(1.6); 2.757(1.7); 2.750(1.3); 2.745(1.2); 2.740 (1.0); 2.734(0.9); 2.727(0.5); 2.723(0.5); 1.850(1.3); 1.811(3.4); 1.763(3.4); 1.715(2.5); 1.686(1.6); 1.677(1.7); 1.660(1.7); 1.651(1.5); 1.642(1.3); 1.631(1.2); 1.622(1.0); 1.602(0.9); 1.592(1.0); 1.566(7.4); 1.331(0.6); 1.288(16.0); 1.265(16.0); 1.206(3.2); 1.160(2.2); 1.127(2.0); 1.099(1.6); 1.089(1.9); 1.059(1.1); 1.050(1.2); 1.020(0.5); 1.006(0.4); 0.903(0.4); 0.882 (1.0); 0.864(1.3); 0.847(3.7); 0.841(4.6); 0.824(4.9); 0.818(3.8); 0.802(1.6); 0.610(1.6); 0.597(3.6); 0.594(3.9); 0.587 (4.7); 0.582(4.1); 0.576(3.7); 0.559(1.3); 0.070(1.2); 0.011(0.6); 0.000(12.0); 0.011(0.7) Example III-85: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.478(2.0); 8.318(3.8); 7.518(1.4); 7.260(256.2); 6.996(1.4); 3.695 (9.8); 3.680(16.0); 3.665(11.3); 1.830(6.2); 1.822(5.4); 1.802(13.7); 1.786(5.2); 1.777(6.2); 1.769(6.8); 1.731(2.6); 1.702 (2.6); 1.554(6.7); 1.348(1.3); 1.316(4.0); 1.292(4.3); 1.285(6.2); 1.261(3.1); 1.253(4.5); 1.245(4.0); 1.238(2.3); 1.222(2.3); 1.215(4.4); 1.207(2.4); 1.192(1.2); 1.184(2.8); 1.177(1.3); 1.153(1.1); 1.144(2.2); 1.107(5.6); 1.078(4.1); 1.053(1.2); 0.008 (3.2); 0.000(102.8); 0.009(2.9) Example III-86: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.262(23.1); 5.298(1.9); 3.720(16.0); 3.689(1.3); 3.673(2.2); 3.659 (1.5); 2.779(1.5); 2.766(1.0); 2.761(1.6); 2.746(0.9); 1.831(0.9); 1.824(0.7); 1.820(0.7); 1.804(1.8); 1.800(1.9); 1.782(0.7); 1.774(0.9); 1.765(1.0); 1.699(0.5); 1.315(0.6); 1.291(0.6); 1.283(0.9); 1.252(0.7); 1.244(0.6); 1.214(0.6); 1.102(0.8); 1.073 (0.6); 0.000(9.1) Example III-87: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.485(2.1); 8.309(4.3); 7.519(1.0); 7.292(0.7); 7.260(178.3); 6.996 (1.0); 3.695(9.8); 3.679(16.0); 3.665(11.3); 1.831(6.3); 1.823(5.3); 1.802(13.9); 1.786(5.3); 1.777(6.3); 1.769(6.9); 1.731 (2.8); 1.702(2.7); 1.607(0.8); 1.357(0.7); 1.348(1.3); 1.339(0.9); 1.317(4.0); 1.292(4.3); 1.285(6.2); 1.261(2.9); 1.253(4.4); 1.245(3.9); 1.238(2.3); 1.222(2.2); 1.215(4.4); 1.207(2.5); 1.192(1.2); 1.184(2.8); 1.177(1.4); 1.154(1.2); 1.145(2.3); 1.107 (5.6); 1.083(4.0); 1.078(4.2); 1.053(1.2); 1.043(0.9); 0.008(2.2); 0.000(74.4); 0.009(2.1) Example III-88: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 9.357(2.8); 8.498(1.9); 7.519(0.8); 7.269(0.9); 7.260(164.1); 6.996 (0.9); 6.441(0.9); 6.300(1.8); 6.161(0.9); 3.850(0.7); 3.845(0.8); 3.701(10.7); 3.685(16.0); 3.671(11.3); 1.864(0.9); 1.839 (6.9); 1.834(7.6); 1.819(7.3); 1.806(14.0); 1.799(10.7); 1.789(5.5); 1.780(6.0); 1.771(7.1); 1.732(3.2); 1.728(2.8); 1.724(2.3); 1.703(3.1); 1.360(0.8); 1.351(1.4); 1.342(0.9); 1.319(4.2); 1.312(3.0); 1.295(4.4); 1.288(6.4); 1.264(2.9); 1.257(4.4); 1.246(3.5); 1.239(2.3); 1.224(2.3); 1.216(4.6); 1.208(2.6); 1.193(1.3); 1.185(2.9); 1.178(1.4); 1.146(2.4); 1.110(5.7); 1.081 (4.6); 1.056(1.3); 1.046(1.0); 0.008(1.8); 0.000(65.3); 0.009(1.9) Example III-89: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.469(1.9); 8.268(2.8); 7.519(1.5); 7.270(1.1); 7.267(2.3); 7.260(271.0); 7.254(1.5); 7.253(1.1); 7.252(0.9); 7.251(0.9); 7.2503(0.7); 7.2495(0.6); 6.996(1.5); 6.244(1.0); 6.108(1.9); 5.974(1.0); 3.861(0.8); 3.851(1.0); 3.845(0.8); 3.806(0.8); 3.697(10.1); 3.681(16.0); 3.667(11.4); 1.832(7.3); 1.827(5.8); 1.804(14.0); 1.778(5.5); 1.769(6.8); 1.733(3.5); 1.702(3.5); 1.358(0.8); 1.349(1.4); 1.340(0.9); 1.318(4.1); 1.293(4.4); 1.286(6.2); 1.262(3.1); 1.255(4.5); 1.245(3.8); 1.238(2.5); 1.223(2.3); 1.215(4.6); 1.207(2.5); 1.192(1.2); 1.184(2.8); 1.177(1.5); 1.145 (2.3); 1.108(5.6); 1.084(4.1); 1.078(4.3); 1.053(1.2); 0.008(3.2); 0.000(108.9); 0.009(3.0) Example III-92: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.471(0.6); 7.455(0.5); 7.261(18.0); 6.910(0.8); 6.905(1.4); 6.889(0.5); 6.884(1.9); 6.863(0.6); 5.027(1.7); 5.013(1.6); 4.094(3.2); 3.550(3.3); 3.527(16.0); 0.000(8.2) Example III-93: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.688(2.1); 8.260(2.6); 7.518(1.8); 7.492(2.5); 7.485(0.8); 7.477(3.1); 7.470(6.0); 7.455(5.4); 7.450(3.5); 7.434(3.2); 7.260(320.9); 6.996(1.8); 6.938(2.5); 6.936(2.1); 6.932(3.4); 6.929(3.9); 6.918(5.4); 6.912(9.5); 6.897(5.1); 6.892(11.4); 6.887(3.9); 6.872(4.7); 6.865(3.1); 6.233(1.1); 6.097(2.1); 5.964(1.1); 5.028 (16.0); 5.014(15.8); 2.703(0.9); 1.562(9.2); 0.008(3.7); 0.000(122.1); 0.009(3.3) Example III-94: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.703(2.3); 8.317(4.2); 7.518(0.9); 7.487(2.6); 7.481(0.8); 7.472(3.3); 7.465(6.1); 7.455(1.2); 7.450(5.6); 7.445(3.7); 7.429(3.3); 7.260(165.3); 6.996(0.9); 6.937(2.6); 6.935(2.3); 6.931(3.6); 6.929(4.1); 6.918(6.1); 6.911(10.8); 6.896(5.7); 6.891(13.1); 6.886(4.0); 6.871(4.9); 6.864(3.3); 5.023(16.0); 5.009(15.8); 1.585(2.6); 0.008(1.9); 0.000(62.6); 0.009(1.8) Example III-95: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.714(0.7); 7.492(0.8); 7.476(1.0); 7.470(1.9); 7.454(1.8); 7.450(1.2); 7.434(1.1); 7.261(65.7); 6.932(0.9); 6.929(0.7); 6.925(1.1); 6.923(1.3); 6.912(2.2); 6.905(3.8); 6.890(1.8); 6.885(4.7); 6.880 (1.3); 6.864(1.6); 6.858(1.1); 5.027(5.1); 5.013(5.1); 3.814(16.0); 3.627(1.2); 0.008(0.7); 0.000(24.8); 0.009(0.7) Example III-96: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.699(2.2); 8.346(3.6); 7.519(0.8); 7.487(2.5); 7.481(0.8); 7.472(3.3); 7.465(6.1); 7.455(1.3); 7.449(5.5); 7.445(3.7); 7.429(3.3); 7.260(154.3); 6.996(0.8); 6.937(2.6); 6.935(2.2); 6.931(3.5); 6.929(4.1); 6.918(6.1); 6.911(10.8); 6.896(5.6); 6.891(13.1); 6.886(4.0); 6.871(4.9); 6.864(3.4); 5.023(16.0); 5.009(15.9); 1.609(2.0); 0.008(1.8); 0.000(58.5); 0.009(1.6) Example IV-12: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.683(2.1); 8.360(1.7); 7.518(7.4); 7.494(2.5); 7.479(3.1); 7.472(5.9); 7.457(5.3); 7.452(3.4); 7.436(3.2); 7.310(0.7); 7.298(0.6); 7.294(0.9); 7.259(1359.9); 7.251(3.7); 7.250(4.1); 7.2493(3.4); 7.2485(2.6); 7.248(2.4); 7.247(2.2); 7.246(1.8); 7.245(1.6); 7.2444(1.5); 7.2436(1.2); 7.243(1.1); 7.242(0.9); 7.241(1.1); 7.240(1.1); 7.239(0.8); 7.237(1.1); 7.236(0.8); 7.233(1.4); 7.229(1.1); 7.226(1.9); 7.222(1.0); 7.210(1.8); 6.995(7.3); 6.937 (2.3); 6.935(2.1); 6.931(3.4); 6.928(3.9); 6.917(5.3); 6.911(9.6); 6.896(5.0); 6.891(11.6); 6.886(3.8); 6.870(4.6); 6.864 (3.1); 6.819(0.8); 6.797(0.8); 5.096(5.6); 5.030(16.0); 5.016(15.9); 4.976(5.1); 3.964(2.1); 3.814(0.7); 3.643(0.5); 3.195 (0.7); 3.178(0.5); 3.161(0.8); 2.806(1.0); 2.789(0.7); 2.771(0.6); 1.532(348.6); 1.499(1.0); 1.284(0.7); 1.256(1.0); 0.146 (1.5); 0.069(1.4); 0.008(15.9); 0.000(538.5); 0.009(14.9); 0.018(0.7); 0.028(0.7); 0.033(0.9); 0.050(0.7); 0.150(1.5) Example IV-19: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.759(1.8); 7.518(12.8); 7.496(2.1); 7.480(2.1); 7.474(4.4); 7.458(4.0); 7.437(2.1); 7.350(2.0); 7.321(1.8); 7.310(3.5); 7.278(4.2); 7.274(5.9); 7.271(7.6); 7.2694(10.1); 7.2686(11.2); 7.268 (12.3); 7.266(17.3); 7.2654(20.0); 7.2646(23.3); 7.264(29.0); 7.259(2343.4); 7.254(33.3); 7.253(15.3); 7.252(10.1); 7.251 (8.7); 7.250(6.1); 7.249(4.9); 7.2484(4.1); 7.2476(4.3); 7.247(3.8); 7.246(3.2); 7.245(2.6); 7.2444(2.0); 7.2437(2.5); 7.243 (1.9); 7.242(1.9); 7.2413(1.9); 7.2405(1.8); 7.240(1.6); 7.237(1.9); 7.227(2.2); 7.210(1.9); 6.995(12.1); 6.937(2.8); 6.926 (3.8); 6.920(6.3); 6.905(3.7); 6.900(8.0); 6.895(3.0); 6.880(3.1); 6.873(2.1); 5.163(15.8); 5.045(16.0); 5.032(11.8); 5.017 (11.0); 3.964(1.3); 1.531(639.6); 1.255(2.3); 0.146(3.0); 0.069(2.6); 0.050(1.6); 0.008(27.0); 0.006(9.8); 0.0054(11.1); 0.0045(12.9); 0.000(903.8); 0.003(44.1); 0.005(13.4); 0.006(10.0); 0.007(7.7); 0.009(25.0); 0.012(2.1); 0.150 (2.3) Example IV-2: .sup.1H-NMR(600.1 MHz, CDCl.sub.3): = 8.450(1.0); 7.262(50.0); 5.300(0.5); 4.663(2.9); 3.685(5.3); 3.675(8.9); 3.665(5.6); 1.833(3.6); 1.813(4.9); 1.810(5.0); 1.804(3.8); 1.798(3.8); 1.792(4.4); 1.786(3.3); 1.771(3.8); 1.721(1.8); 1.705(1.6); 1.700(1.9); 1.604(2.9); 1.328(1.0); 1.323(0.6); 1.313(2.0); 1.308(3.2); 1.291(2.4); 1.286(4.0); 1.281(2.2); 1.270(1.2); 1.265(2.0); 1.260(1.2); 1.237(0.9); 1.232(1.5); 1.227(0.8); 1.217(1.3); 1.212(2.5); 1.206(1.3); 1.196(1.0); 1.191(1.8); 1.185(1.0); 1.175(0.4); 1.170(0.6); 1.164(0.3); 1.125(1.3); 1.120(1.2); 1.104(3.3); 1.100(3.1); 1.084(2.9); 1.080(2.8); 1.062(0.9); 0.000(16.9); 0.006(0.7) Example IV-23: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.469(2.3); 8.198(4.0); 7.518(1.1); 7.260(184.0); 6.995(1.0); 3.851 (0.6); 3.698(8.2); 3.682(14.8); 3.668(8.8); 1.833(8.1); 1.805(16.0); 1.770(7.4); 1.733(3.3); 1.703(3.3); 1.594(5.6); 1.349(1.5); 1.318(4.5); 1.286(6.4); 1.254(4.5); 1.215(3.8); 1.185(2.5); 1.143(2.7); 1.109(6.4); 1.080(5.0); 0.000(66.2) Example IV-3: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.684(1.6); 7.518(3.4); 7.478(2.8); 7.464(5.5); 7.460(6.0); 7.445(3.2); 7.441(3.3); 7.380(1.6); 7.376(1.7); 7.366(1.9); 7.361(3.8); 7.356(3.0); 7.347(3.0); 7.341(4.3); 7.336(2.5); 7.327(2.5); 7.323 (2.2); 7.291(1.1); 7.259(569.8); 7.210(0.6); 7.188(4.9); 7.185(5.6); 7.169(7.7); 7.166(9.3); 7.150(7.5); 7.147(7.3); 7.129 (4.0); 7.124(5.5); 7.103(3.5); 6.995(3.2); 5.154(0.9); 5.069(16.0); 5.055(15.9); 4.644(4.4); 4.114(0.9); 3.868(0.7); 3.805 (0.9); 1.575(11.4); 1.242(2.2); 0.146(0.6); 0.008(6.2); 0.000(225.1); 0.009(7.4); 0.150(0.6) Example IV-4: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.508(1.4); 7.518(3.4); 7.466(0.6); 7.441(1.1); 7.420(0.7); 7.397(7.5); 7.392(3.4); 7.384(7.9); 7.375(9.2); 7.367(3.7); 7.362(8.8); 7.305(0.7); 7.284(1.0); 7.259(641.8); 7.209(1.2); 7.140(0.9); 7.121 (1.6); 7.113(11.5); 7.108(3.6); 7.097(3.7); 7.092(20.1); 7.086(4.0); 7.075(3.4); 7.070(9.8); 7.062(1.2); 6.995(4.2); 6.978 (2.2); 6.956(1.4); 6.899(1.5); 6.878(1.4); 5.046(2.5); 4.959(15.9); 4.946(16.0); 4.613(1.3); 4.598(1.3); 4.550(0.8); 4.115 (1.3); 3.864(1.7); 3.850(2.2); 3.837(1.5); 3.807(6.7); 3.161(1.0); 3.144(0.9); 3.127(1.1); 2.755(1.3); 2.738(0.8); 2.721 (1.0); 2.707(0.7); 1.741(3.6); 1.243(3.5); 0.157(0.6); 0.146(0.6); 0.008(6.0); 0.000(229.8); 0.009(7.2); 0.150(0.9) Example IV-5: .sup.1H-NMR(600.1 MHz, CDCl.sub.3): = 8.664(0.6); 7.487(0.7); 7.473(1.5); 7.462(1.5); 7.448(0.8); 7.261(50.0); 6.916(0.9); 6.901(3.1); 6.893(0.7); 6.887(2.3); 6.881(1.0); 6.870(1.1); 6.866(0.8); 5.098(0.5); 5.026(5.1); 5.017(5.0); 4.662(1.0); 1.640(1.7); 0.005(0.8); 0.000(16.9) Example IV-6: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.518(1.0); 7.259(190.7); 7.248(1.2); 7.235(0.9); 7.227(1.4); 7.224(1.5); 7.203(2.6); 7.184(1.7); 7.178(1.8); 7.159(1.7); 7.146(1.1); 7.138(1.2); 6.995(1.1); 5.298(16.0); 4.969(4.9); 4.956(4.9); 4.663(1.7); 3.804(0.6); 1.538(15.4); 1.432(0.9); 0.008(2.1); 0.000(71.6); 0.009(2.1) Example IV-7: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.574(1.9); 7.823(0.5); 7.518(3.3); 7.359(0.5); 7.259(635.3); 7.222(0.6); 7.210(0.7); 6.996(3.7); 6.870(0.7); 6.781(1.2); 6.773(2.2); 6.766(10.7); 6.760(1.7); 6.747(13.9); 6.744(14.2); 6.731(1.8); 6.725(10.7); 6.718(2.4); 6.710(1.3); 6.649(1.1); 6.628(1.5); 6.608(1.1); 5.298(2.1); 5.082(2.8); 5.042(16.0); 5.029(15.9); 4.650(3.4); 4.118(0.7); 3.876(1.4); 3.863(1.7); 3.814(3.4); 3.152(1.2); 3.135(1.2); 3.128(0.7); 3.117(1.5); 2.789(1.6); 2.780 (0.6); 2.772(1.2); 2.755(1.2); 1.652(4.6); 1.256(2.2); 0.146(0.6); 0.008(7.0); 0.000(244.8); 0.009(7.4); 0.149(0.7) Example IV-9: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 8.475(2.0); 8.362(1.7); 7.519(2.6); 7.311(0.6); 7.2714(1.4); 7.2707(1.4); 7.268(2.4); 7.260(481.1); 7.254(3.6); 7.253(2.7); 7.252(1.8); 7.251(1.5); 7.2504(1.4); 7.2496(1.2); 7.249(0.9); 7.248 (0.8); 7.2472(0.8); 7.2465(0.7); 7.246(0.6); 6.996(2.5); 5.104(4.3); 4.986(4.4); 3.697(10.0); 3.681(16.0); 3.667(11.3); 1.833 (6.2); 1.827(5.1); 1.805(13.2); 1.791(5.6); 1.777(4.9); 1.769(6.1); 1.730(2.7); 1.701(2.7); 1.543(50.0); 1.349(1.4); 1.317 (4.1); 1.293(4.4); 1.285(6.3); 1.262(3.1); 1.254(4.8); 1.244(3.8); 1.237(2.4); 1.223(2.2); 1.215(4.6); 1.207(2.5); 1.184(2.8); 1.144(2.4); 1.108(5.5); 1.078(4.3); 1.053(1.3); 0.008(4.7); 0.006(1.5); 0.005(1.7); 0.000(168.4); 0.006(2.0); 0.007 (1.6); 0.009(4.8) Example V-10: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.992(15.0); 7.988(15.9); 7.982(15.8); 7.979(16.0); 7.750(14.9); 7.747 (15.1); 7.737(15.7); 7.734(15.3); 7.260(44.9); 7.209(15.9); 7.199(16.2); 7.196(16.2); 7.187(14.7); 3.804(0.5); 3.799(0.6); 3.735(0.8); 0.000(17.3); 0.008(0.7) Example V-11: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.519(1.0); 7.403(1.5); 7.387(1.7); 7.381(3.2); 7.365(3.3); 7.360(1.8); 7.344(1.7); 7.260(183.1); 6.996(1.0); 6.888(1.4); 6.885(1.4); 6.882(1.6); 6.879(1.6); 6.865(2.2); 6.859(2.6); 6.846(1.3); 6.844(1.3); 6.840(1.5); 6.837(1.5); 6.824(2.5); 6.818(1.9); 6.802(2.7); 6.798(2.8); 6.796(2.3); 6.792(2.2); 6.777(2.4); 6.770 (2.0); 5.075(16.0); 4.817(6.1); 3.240(0.8); 1.682(5.0); 1.668(10.1); 1.660(10.9); 1.658(6.6); 1.646(5.9); 1.604(0.7); 1.545 (9.1); 1.392(0.6); 1.351(5.9); 1.339(6.7); 1.336(10.9); 1.329(10.2); 1.315(4.7); 1.256(1.9); 0.126(0.8); 0.008(2.2); 0.000 (72.0); 0.009(1.9) Example V-12: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.518(1.6); 7.454(1.5); 7.438(1.7); 7.432(3.2); 7.417(3.2); 7.411(1.8); 7.395(1.6); 7.292(0.6); 7.278(0.6); 7.271(1.4); 7.270(1.5); 7.269(2.0); 7.267(2.5); 7.260(298.6); 6.996(1.7); 6.892(1.4); 6.889(1.4); 6.886(1.6); 6.883(1.6); 6.869(2.2); 6.863(2.5); 6.850(1.3); 6.848(1.3); 6.844(1.5); 6.841(1.5); 6.826(2.5); 6.820 (2.0); 6.804(2.7); 6.801(2.8); 6.798(2.3); 6.794(2.2); 6.779(2.4); 6.773(2.0); 5.074(16.0); 4.802(4.8); 1.543(10.1); 1.491 (1.9); 1.475(3.8); 1.473(3.5); 1.470(2.8); 1.466(4.3); 1.464(3.5); 1.455(5.2); 1.453(5.8); 1.446(4.4); 1.444(3.3); 1.431(2.6); 1.408(0.6); 1.387(0.5); 1.371(0.5); 1.326(3.0); 1.315(3.2); 1.312(4.1); 1.305(3.2); 1.303(3.6); 1.288(2.0); 1.281(3.0); 1.270 (3.5); 1.267(4.4); 1.260(4.2); 1.258(5.9); 1.243(2.0); 0.069(1.7); 0.027(0.8); 0.008(3.5); 0.000(115.7); 0.009(3.1) Example V-13: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.763(4.4); 7.762(5.2); 7.760(4.5); 7.758(3.2); 7.681(2.5); 7.680(2.8); 7.677(2.2); 7.675(1.8); 7.671(2.4); 7.668(3.0); 7.667(3.0); 7.665(3.1); 7.663(3.2); 7.662(3.4); 7.660(3.5); 7.658(2.8); 7.656 (2.3); 7.651(2.9); 7.648(3.3); 7.572(1.5); 7.556(1.7); 7.551(3.2); 7.535(3.1); 7.530(1.7); 7.519(0.6); 7.514(1.6); 7.473 (2.2); 7.471(2.9); 7.470(2.1); 7.451(4.6); 7.432(2.0); 7.260(82.5); 6.928(1.3); 6.925(1.3); 6.922(1.4); 6.919(1.4); 6.906(2.1); 6.899(2.3); 6.887(1.2); 6.884(1.2); 6.880(1.3); 6.877(1.4); 6.839(2.2); 6.832(1.8); 6.817(2.3); 6.813(2.5); 6.811(2.2); 6.807 (2.0); 6.791(2.2); 6.785(1.9); 5.298(1.3); 5.211(16.0); 4.579(4.1); 1.561(0.6); 0.008(0.9); 0.000(30.7); 0.009(0.9) Example V-14: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.880(0.6); 7.553(1.5); 7.537(1.7); 7.532(3.1); 7.516(3.1); 7.510(1.7); 7.495(1.6); 7.418(2.0); 7.412(2.2); 7.400(2.1); 7.393(3.3); 7.387(2.2); 7.374(1.9); 7.369(2.1); 7.285(1.4); 7.282(1.5); 7.280 (1.4); 7.275(1.8); 7.271(1.9); 7.269(1.9); 7.260(83.9); 7.255(2.5); 7.250(1.8); 7.248(1.7); 7.245(1.5); 7.137(2.4); 7.118 (2.6); 7.115(2.3); 7.113(2.7); 7.096(2.2); 7.094(2.7); 7.091(2.1); 7.072(1.7); 6.921(1.3); 6.919(1.3); 6.915(1.4); 6.912(1.4); 6.899(2.1); 6.893(2.3); 6.880(1.2); 6.877(1.2); 6.873(1.3); 6.871(1.3); 6.833(2.2); 6.827(1.8); 6.811(2.3); 6.808(2.5); 6.805 (2.2); 6.802(2.0); 6.786(2.1); 6.780(1.8); 5.298(8.8); 5.172(16.0); 4.667(3.3); 0.008(0.9); 0.000(31.4); 0.009(0.9) Example V-15: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.624(0.5); 7.615(2.3); 7.594(14.9); 7.586(16.0); 7.579(2.3); 7.563(3.1); 7.546(1.6); 7.540(2.9); 7.525(2.9); 7.519(2.0); 7.503(1.4); 7.260(70.0); 6.928(1.2); 6.925(1.2); 6.921(1.3); 6.918(1.3); 6.905(2.0); 6.899(2.2); 6.886(1.1); 6.883(1.1); 6.880(1.2); 6.877(1.2); 6.839(1.9); 6.832(1.7); 6.817(2.1); 6.813(2.3); 6.811 (2.1); 6.807(1.9); 6.791(1.9); 6.785(1.7); 5.298(1.0); 5.195(15.1); 4.615(3.5); 0.008(0.8); 0.000(27.1); 0.009(0.9) Example V-16: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.550(1.5); 7.534(1.7); 7.529(3.1); 7.519(0.6); 7.513(3.1); 7.508(1.7); 7.492(1.6); 7.260(79.6); 7.046(0.9); 7.040(0.7); 7.032(5.5); 7.029(3.7); 7.027(6.4); 7.023(3.6); 7.018(3.5); 7.015(6.3); 7.009 (5.5); 7.001(0.6); 6.996(1.2); 6.929(1.3); 6.926(1.3); 6.923(1.4); 6.920(1.4); 6.906(2.2); 6.903(3.3); 6.900(2.6); 6.898 (3.7); 6.892(1.4); 6.888(1.4); 6.885(1.6); 6.882(3.9); 6.876(5.4); 6.871(2.5); 6.861(1.6); 6.855(2.6); 6.849(1.2); 6.842(2.2); 6.836(1.8); 6.820(2.4); 6.817(2.5); 6.814(2.2); 6.811(2.0); 6.795(2.2); 6.789(1.8); 5.298(0.7); 5.171(16.0); 4.664(3.3); 0.008 (0.9); 0.000(29.4); 0.009(0.8) Example V-8: .sup.1H-NMR(400.0 MHz, d.sub.6-DMSO): = 10.835(0.4); 8.311(1.1); 7.959(0.4); 7.957(0.4); 7.917(0.4); 7.914 (0.5); 7.893(7.1); 7.891(8.1); 7.889(8.0); 7.887(7.0); 7.844(0.5); 7.842(0.5); 7.532(1.5); 7.515(2.0); 7.510(3.3); 7.493(3.3); 7.488(2.1); 7.472(1.7); 7.373(0.7); 7.364(0.6); 7.281(6.8); 7.279(6.9); 7.272(8.7); 7.270(8.2); 7.265(2.4); 7.248(2.6); 7.245 (2.9); 7.242(2.9); 7.239(2.6); 7.222(2.0); 7.215(2.1); 7.138(2.1); 7.132(1.7); 7.117(3.2); 7.112(3.0); 7.095(1.6); 7.091 (1.5); 6.714(0.4); 6.701(0.3); 6.642(0.6); 6.634(6.1); 6.630(6.2); 6.625(6.1); 6.621(5.9); 6.585(0.4); 6.553(10.0); 5.146(0.9); 5.084(15.6); 4.428(0.6); 4.412(0.5); 3.952(0.8); 3.920(0.3); 3.901(16.0); 3.854(1.5); 3.510(0.4); 3.478(0.4); 3.467(0.4); 3.334(883.6); 3.170(0.8); 2.696(0.5); 2.676(1.6); 2.672(2.2); 2.667(1.6); 2.542(1.0); 2.525(5.9); 2.512(139.3); 2.507(280.6); 2.503(368.9); 2.498(273.9); 2.494(137.6); 2.334(1.6); 2.329(2.2); 2.325(1.6); 2.321(0.8); 1.236(0.4); 0.000(8.5); 0.008 (0.3) Example V-9: .sup.1H-NMR(400.0 MHz, CDCl.sub.3): = 7.518(8.2); 7.437(2.8); 7.416(5.7); 7.400(5.8); 7.378(4.1); 7.259(1434.0); 7.210(2.0); 7.027(2.5); 6.995(8.4); 6.894(3.5); 6.874(11.9); 6.861(2.8); 6.853(8.5); 6.827(4.2); 6.821(3.1); 4.728(5.3); 4.661(16.0); 4.646(15.1); 3.244(1.8); 1.539(16.7); 1.256(1.8); 0.331(1.9); 0.237(1.6); 0.157(2.6); 0.146(2.2); 0.008(19.8); 0.000(539.9); 0.008(20.0); 0.150(2.0)

    B) Formulation Examples

    [0529] a) A dust is obtained by mixing 10 parts by weight of a compound of the formula (G) and 90 parts by weight of talc as inert substance and comminuting the mixture in a hammer mill. [0530] b) A wettable powder which is readily dispersible in water is obtained by mixing 25 parts by weight of a compound of the formula (G), 64 parts by weight of kaolin-containing quartz as inert substance, 10 parts by weight of potassium lignosulphonate and 1 part by weight of sodium oleoylmethyltaurate as wetting agent and dispersant, and grinding the mixture in a pinned-disk mill. [0531] c) A readily water-dispersible dispersion concentrate is obtained by mixing 20 parts by weight of a compound of the formula (G) with 6 parts by weight of alkylphenol polyglycol ether (Triton X 207), 3 parts by weight of isotridecanol polyglycol ether (8 EO) and 71 parts by weight of paraffinic mineral oil (boiling range for example about 255 to above 277 C.) and grinding the mixture in a ball mill to a fineness of below 5 microns. [0532] d) An emulsifiable concentrate is obtained from 15 parts by weight of a compound of the formula (G), 75 parts by weight of cyclohexanone as solvent and 10 parts by weight of oxyethylated nonylphenol as emulsifier. [0533] e) Water-dispersible granules are obtained by mixing [0534] 75 parts by weight of a compound of the formula (G), [0535] 10 parts by weight of calcium lignosulphonate, [0536] 5 parts by weight of sodium laurylsulphate, [0537] 3 parts by weight of polyvinyl alcohol and [0538] 7 parts by weight of kaolin, [0539] grinding the mixture in a pinned-disk mill, and granulating the powder in a fluidized bed by spray application of water as a granulating liquid. [0540] f) Water-dispersible granules are also obtained by homogenizing and precomminuting [0541] 25 parts by weight of a compound of the formula (G), [0542] 5 parts by weight of sodium 2,2-dinaphthylmethane-6,6-disulphonate, [0543] 2 parts by weight of sodium oleoylmethyltaurinate, [0544] 1 part by weight of polyvinyl alcohol, [0545] 17 parts by weight of calcium carbonate and [0546] 50 parts by weight of water, [0547] on a colloid mill, subsequently grinding the mixture in a bead mill and atomizing and drying the resulting suspension in a spray tower by means of a single-substance nozzle.

    (C) Biological Examples

    [0548] 1. Herbicidal pre-emergence action

    [0549] Seeds of monocotyledonous and dicotyledonous weed plants and crop plants were placed in wood-fibre pots in sandy loam and covered with soil. The compounds (G) according to the invention, formulated in the form of wettable powders (WP), were then applied as aqueous suspension or emulsion at a water application rate of 600 I/ha (converted) with the addition of 0.2% of wetting agent to the surface of the covering soil.

    [0550] After the treatment, the pots were placed in a greenhouse and kept under good growth conditions for the test plants. After about 3 weeks, the effect of the preparations was scored visually in comparison with untreated controls as percentages. For example, 100% activity=the plants have died, 50% herbicidal activity or damage=the plants have been reduced by 50% or the plant mass has been reduced by 50%, 0% activity=like control plants.

    [0551] Compounds (G) according to the invention such as, for example, the compounds No. I-9, I-10, I-11, I-13, I-16, I-17, I-20, I-21, I-23, I-24, I-25, I-26, I-27, I-28, I-29, I-30, I-31, I-32, I-33, I-34, I-35, I-36, I-37, I-38, I-39, I-40, I-41, I-44, I-46, I-48, I-53, I-86, I-96, I-103, I-104, I-107, I-109, I-111, I-120, I-127, I-168, I-186, I-209, I-227, I-250, I-254, I-258, I-268, I-291, I-332, I-350, I-373, I-391, I-414, I-432, I-455, I-473, I-495, I-497, I-504, I-506, I-509, I-517, I-524, I-527, I-528, I-534, I-535, I-537, I-540, I-541, II-5, II-8, II-9, II-10, II-13, II-14, II-15, II-22, II-28, II-29, II-35, II-36, II-50, II-55, II-56, II-57, II-62, II-63, II-64, II-70, II-71, II-77, II-78, II-84, II-85, II-91, II-92, II-98, II-99, II-105, II-106, II-111, II-112, II-113, II-119, II-120, II-126, II-127, II-133, II-134, II-140, II-141, II-147, II-148, II-155, II-168, II-183, II-189, II-196, II-204, II-211, II-217, II-224, II-225, II-232, II-233, II-248, II-249, II-250, II-251, II-255, II-256, II-257, II-258, II-259, II-260, II-261, II-262, II-264, II-265, II-266, II-279, II-281, II-282, II-283, II-284, II-286, II-287, II-288, II-289, II-290, II-292, II-293, II-294, II-295, II-297, II-299, II-300, II-301, II-302, II-303, II-304, II-306, II-307, II-308, II-309, II-311, II-312, II-313, II-314, II-315, II-316, II-326, II-327, II-329, II-330, II-332, II-334, II-335, II-336, II-337, II-338, II-340, II-341, II-342, II-343, II-346, II-347, II-348, II-349, II-350, II-351, II-352, II-353, II-354, II-355, II-356, II-357, II-358, II-359, II-360, II-361, II-363, II-364, II-365, II-366, II-367, II-374, II-376, II-379, II-380, II-382, II-385, II-386, II-387, II-388, II-389, II-390, II-398, II-399, II-400, II-401, II-402, II-413, II-417, II-419, III-420, II-421, II-422, II-424, II-425, II-426, II-427, II-428, II-429, II-430, II-437, II-438, II-439, III-19, III-32, III-42, III-43, III-46, III-52, III-62, III-85, III-86, III-87, III-88, 111-89, III-92, III-93, III-94, III-95, III-96, IV-2, IV-3, IV-4, IV-5, IV-6, IV-7, IV-9, IV-12, IV-19, IV-23, V-8, V-9, V-10, V-11, V-12, V-13 and V-16 from the above Tables 1 to 5, have good herbicidal efficacy (70% to 100% activity) against a plurality of harmful plants at an application rate of 320 g or less of active substance per hectare when applied by the pre-emergence method, in particular against against one, two, three, four, five, six, seven, eight, nine, ten or more, or even all of the harmful plants selected from the group consisting of

    ALOMY=Alopecurus myosuroides
    AVEFA=Avena fatua
    ECHCG=Echinochloa crus-galli
    LOLMU=Lolium multiflorum
    SETVI=Setaria viridis
    ABUTH=Abutilon theophrasti
    AMARE=Amaranthus retroflexus
    MATIN=Matricaria inodora (=Tripleurospermum maritimum subsp. inodorum)
    PHBPU=Pharbitis purpurea
    POLCO=Polygonum convolvulus (=Fallopia convolvulus)
    STEME=Stellaria media
    VIOTR=Viola tricolor
    VERPE=Veronica persica

    [0552] What was determined was the respective herbicidal activity, in each case at the same point in time after application of the formulation in question, i.e. the damage to the respective harmful plant in % compared to untreated control plants.

    [0553] The compounds No. I-9, I-17, I-20, I-21, I-23, I-25, I-27, I-32, I-33, I-34, I-35, I-36, I-38, I-44, I-86, I-109, I-209, I-227, II-15, II-22, II-29, II-36, II-50, II-57, II-64, II-70, II-71, II-78, II-84, II-85, II-91, II-92, II-98, II-99, II-105, II-106, II-112, II-113, II-119, II-120, II-126, II-127, II-133, II-134, II-140, II-141, II-147, II-148, II-155, II-183, II-196, II-204, II-211, II-217, II-225, V-8, V-9 and V-10 showed excellent activity (90-100%) against several harmful plants when applied by the pre-emergence method at an application rate of 320 g of active substance per hectare, and showed very good activity (80-100%) against several harmful plants when applied by the pre-emergence method at an application rate of 80 g of active substance per hectare, in particular against two, three, four or more harmful plants selected from the group consisting of ALOMY, AVEFA, ECHCG, LOLMU, SETVI, ABUTH, AMARE, MATIN, PHBPU, POLCO, STEME, VIOTR and VERPE.

    [0554] Similarly, the compounds No. I-495, I-497, I-504, I-506, I-524, I-527, I-528, I-534, I-535, I-537, I-540, II-28, II-56, II-63, II-233, II-248, II-249, II-250, II-251, II-255, II-256, II-257, II-258, II-259, II-260, II-261, II-264, II-265, II-266, II-279, II-281, II-282, II-283, II-284, II-286, II-287, II-288, II-289, II-290, II-294, II-295, II-297, II-299, II-300, II-301, II-302, II-303, II-304, II-306, II-307, II-308, II-309, II-311, II-312, II-314, II-327, II-329, II-330, II-332, II-334, II-335, II-337, II-338, II-340, II-341, II-342, II-343, II-346, II-347, II-348, II-349, II-350, II-351, II-352, II-353, II-354, II-355, II-356, II-359, II-363, II-365, II-366, II-367, II-374, II-379, II-380, II-382, II-386, II-387, II-388, II-389, II-390, II-401, II-413, II-419, 111-420, II-421, II-422, II-424, II-425, I-427, II-428, II-429, II-430, II-437, II-438, II-439, III-85, III-89, V-12 and V-16 showed excellent activity (90-100%) against several harmful plants when applied by the pre-emergence method at an application rate of 320 g of active substance per hectare, and showed very good activity (80-100%) against several harmful plants when applied by the pre-emergence method at an application rate of 80 g of active substance per hectare, in particular against two, three, four or more harmful plants selected from the group consisting of ALOMY, AVEFA, ECHCG, LOLMU, SETVI, ABUTH, AMARE, MATIN, PHBPU, POLCO, STEME, VIOTR and VERPE.

    [0555] The compounds according to the invention displayed particularly good herbicidal activity in pre-emergence application method against several harmful plants selected from the group ALOMY=Alopecurus myosuroides, ECHCG=Echinochloa crus-galli, SETVI=Setaria viridis, ABUTH=Abutilon theophrasti, AMARE=Amaranthus retroflexus, PHBPU=Pharbitis purpurea, POLCO=Polygonum convolvulus, VIOTR=Viola tricolor and VERPE=Veronica persica.

    [0556] 2. Herbicidal Post-Emergence Action

    [0557] Seeds of monocotyledonous and dicotyledonous weeds and crop plants were placed in sandy loam in wood-fibre pots, covered with soil and cultivated in a greenhouse under good growth conditions. 2 to 3 weeks after sowing, the test plants were treated at the one-leaf stage, where the compounds (G) according to the invention, formulated in the form of wettable powders (WP), were applied by spraying as aqueous suspension or emulsion at a water application rate of 6001/ha (converted) with the addition of 0.2% of wetting agent to the green parts of the plants. After the test plants had been kept in the greenhouse under optimum growth conditions for about 3 weeks, the activity of the preparations was rated visually in comparison to untreated controls in percent (%): For example, 100% activity=the plants have died, 50% herbicidal activity or damage=the plants have been reduced by 50% or the plant mass has been reduced by 50%, 0% activity=like control plants.

    [0558] Compounds (G) according to the invention such as, for example, the compounds No. I-9, I-10, I-11, I-13, I-16, I-17, I-20, I-21, I-23, I-24, I-25, I-26, I-27, I-28, I-29, I-30, I-31, I-32, I-33, I-34, I-35, I-36, I-37, I-38, I-39, I-40, I-41, I-44, I-46, I-48, I-53, I-86, I-96, I-103, I-104, I-107, I-109, I-111, I-120, I-127, I-168, I-186, I-209, I-227, I-250, I-254, I-258, I-268, I-291, I-332, I-350, I-373, I-391, I-414, I-432, I-455, I-473, I-495, I-497, I-504, I-506, I-513, I-515, I-516, I-517, I-518, I-524, I-527, I-528, I-534, I-535, I-540, I-541, II-5, II-8, II-9, II-10, II-13, II-14, II-15, II-22, II-28, II-29, II-35, II-36, II-50, II-55, II-56, II-57, II-63, II-64, II-70, II-71, II-77, II-78, II-84, II-85, II-91, II-92, II-98, II-99, II-105, II-106, II-111, II-112, II-113, II-119, II-120, II-126, II-127, II-133, II-134, II-140, II-141, II-147, II-148, II-155, II-168, II-183, II-189, II-196, II-204, II-211, II-217, II-224, II-225, II-232, II-233, II-248, II-249, II-250, II-251, II-255, II-256, II-257, II-258, II-259, II-260, II-261, II-262, II-264, II-265, II-266, II-279, II-281, II-282, II-283, II-284, II-286, II-287, II-288, II-289, II-290, II-292, II-293, II-294, II-295, II-297, II-299, II-300, II-301, II-302, II-303, II-304, II-306, II-307, II-308, II-309, II-311, II-312, II-313, II-314, II-315, II-316, II-317, II-318, II-320, II-321, II-326, II-327, II-329, II-330, II-332, II-334, II-335, II-337, II-338, II-340, II-341, II-342, II-346, II-347, II-348, II-349, II-350, II-351, II-352, II-353, II-354, II-355, II-356, II-357, II-358, II-359, II-360, II-361, II-362, II-363, II-364, II-365, II-366, II-367, II-369, II-374, II-376, II-379, II-380, II-382, II-385, II-386, II-387, II-388, II-389, II-390, II-392, II-393, II-394, II-395, II-398, II-399, II-400, II-401, II-402, II-403, II-405, II-417, II-419, II-420, II-422, II-424, II-425, II-426, II-427, II-428, II-429, II-430, II-437, II-439, III-19, III-32, III-42, III-43, III-46, III-52, III-62, III-85, III-86, III-88, III-89, III-92, III-93, III-96, IV-2, IV-3, IV-4, IV-5, IV-6, IV-7, IV-9, IV-12, IV-19, IV-23, V-8, V-9, V-10, V-11, V-12 and V-16 from the above Tables 1 to 5, have good herbicidal efficacy (70% to 100% activity) against a plurality of harmful plants at an application rate of 320 g or less of active substance per hectare when applied by the pre-emergence method, in particular against against one, two, three, four, five, six, seven, eight, nine, ten or more, or even all of the harmful plants selected from the group consisting of ALOMY, AVEFA, ECHCG, LOLMU, SETVI, ABUTH, AMARE, MATIN, PHBPU, POLCO, STEME, VIOTR and VERPE.

    [0559] What was determined was the respective herbicidal activity, in each case at the same point in time after application of the formulation in question, i.e. the damage to the respective harmful plant in % compared to untreated control plants.

    [0560] The compounds No. 1-9, I-20, I-23, I-25, I-26, I-32, I-33, I-35, I-36, I-38, I-86, I-104, I-109, I-209, I-227, II-22, II-29, II-50, II-57, II-70, II-71, II-78, II-84, II-85, II-91, II-92, II-98, II-99, II-105, II-106, II-112, II-113, II-119, II-120, II-126, II-127, II-133, II-140, II-147, II-148, II-183, II-196, II-211, II-217, II-225, V-8, V-9 and V-10 showed excellent activity (90-100%) against several harmful plants when applied by the post-emergence method at an application rate of 320 g of active substance per hectare, and showed very good activity (80-100%) against several harmful plants when applied by the post-emergence method at an application rate of 80 g of active substance per hectare, in particular against two, three, four or more harmful plants selected from the group consisting of ALOMY, AVEFA, ECHCG, LOLMU, SETVI, ABUTH, AMARE, MATIN, PHBPU, POLCO, STEME, VIOTR and VERPE.

    [0561] Similarly, the compounds No. 1-495, I-497, I-506, I-515, I-517, I-524, I-527, I-528, I-534, I-535, I-540, I-541, II-28, II-35, II-56, II-63, II-77, II-233, II-248, II-249, II-251, II-255, II-256, II-257, II-258, II-259, II-260, II-261, II-262, II-264, II-265, II-266, II-281, II-282, II-283, II-284, II-286, II-287, II-288, II-289, II-290, II-292, II-293, II-294, II-295, II-297, II-299, II-300, II-301, II-302, II-303, II-304, II-306, II-307, II-308, II-309, II-311, II-312, II-313, II-314, II-315, II-316, II-317, II-318, II-320, II-321, II-326, II-327, II-329, II-330, II-332, II-334, II-335, II-337, II-338, II-340, II-341, II-342, II-346, II-347, II-348, II-349, II-350, II-351, II-352, II-355, II-356, II-357, II-358, II-359, II-360, II-361, II-362, II-363, II-366, II-367, II-374, II-376, II-379, II-380, II-382, II-386, II-387, II-392, II-393, II-394, II-398, II-399, II-400, II-402, II-417, II-419, II-420, II-422, II-424, II-425, II-427, II-428, II-429, II-430, II-437, II-439, III-85, III-89, III-92, III-93, III-96, V-11 and V-16 showed excellent activity (90-100%) against several harmful plants when applied by the post-emergence method at an application rate of 320 g of active substance per hectare, and showed very good activity (80-100%) against several harmful plants when applied by the post-emergence method at an application rate of 80 g of active substance per hectare, in particular against two, three, four or more harmful plants selected from the group consisting of ALOMY, AVEFA, ECHCG, LOLMU, SETVI, ABUTH, AMARE, MATIN, PHBPU, POLCO, STEME, VIOTR and VERPE. The compounds according to the invention displayed particularly good herbicidal activity in post-emergence application method against several harmful plants selected from the group ECHCG=Echinochloa crus-galli, SETVI=Setaria viridis, ABUTH=Abutilon theophrasti, AMARE=Amaranthus retroflexus, PHBPU=Pharbitis purpurea, POLCO=Polygonum convolvulus, STEME=Stellaria media, VIOTR=Viola tricolor and VERPE=Veronica persica, in some cases with a particular pronounced herbicidal activity against ABUTH, AMARE, PHBPU, POLCO, VIOTR and VERPE.

    [0562] 3. Herbicidal Action and Crop Plant Compatibility

    [0563] In further trials in the greenhouse, seeds of crop plants are placed in pots in sandy loam soil, covered with soil and cultivated under good growth conditions and treated by the pre-emergence method and scored analogously to the harmful plants mentioned in above section (C) examples 1 and 2, respectively.

    [0564] 3.1 The results showed that the compounds according to the invention did not cause significant damage when applied by the pre-emergence method at the same application rates as mentioned above to monocotyledonous crops, such as

    [0565] ORYSA=Oryza sativa (common rice)

    [0566] TRZAS=Triticum aestivum (spring) (summer wheat)

    [0567] ZEAMX=Zea mays (maize)

    [0568] BRSNW=Brassica napus subsp. napus (winter) (winter oilseed rape)

    [0569] Here, the observed damage to the respective useful plants was within the acceptable range and was generally assessed as low (generally in a range from 0 to 10%).

    [0570] 3.2 The results showed that the compounds according to the invention did not cause significant damage when applied by the post-emergence method at the same application rates as mentioned above to monocotyledonous crops, such as those mentioned in above section (C) 3.1.

    [0571] Here, the observed damage to the respective useful plants was within the acceptable range and was generally assessed as low (generally in a range from 0 to 20%).