C07C255/46

HYDROXYNORKETAMINE ANALOGUES, COMPOSITIONS COMPRISING SAME AND METHODS OF USE THEREOF
20230265046 · 2023-08-24 ·

The present disclosure pertains to amino cyclohexanone compounds, pharmaceutical compositions containing same and methods of treating depression, pain, inflammation, and other clinical indications.

Compositions and methods for visible-light-controlled ruthenium-catalyzed olefin metathesis

The present disclosure provides compositions and methods for metathesizing a first alkenyl or alkynyl group with a second alkenyl or alkynyl group, the composition comprising a ruthenium metathesis catalyst and a photoredox catalyst that is activated by visible light.

Compositions and methods for visible-light-controlled ruthenium-catalyzed olefin metathesis

The present disclosure provides compositions and methods for metathesizing a first alkenyl or alkynyl group with a second alkenyl or alkynyl group, the composition comprising a ruthenium metathesis catalyst and a photoredox catalyst that is activated by visible light.

COMPOUND
20220144769 · 2022-05-12 ·

A compound represented by Formula (I) is provided:

##STR00001##

In Formula (I), R.sup.3, R.sup.4, and R.sup.5 each independently represent an electron-withdrawing group; R.sup.1, R.sup.2, R.sup.6, and R.sup.7 each independently represent a hydrogen atom, a heterocyclic group, a halogen atom, a nitro group, a cyano group, a hydroxy group, a thiol group, a carboxy group, —SCF.sub.3, —SF.sub.5, —SF.sub.3, —SO.sub.3H, —SO.sub.2H, an aliphatic hydrocarbon group having 1 to 25 carbon atoms which may have a substituent, or an aromatic hydrocarbon group having 6 to 18 carbon atoms which may have a substituent; and R.sup.1 and R.sup.2, R.sup.1 and R.sup.6, R.sup.6 and R.sup.7, and R.sup.4 and R.sup.5 may be linked to each other to form a ring.

COMPOUND
20220144769 · 2022-05-12 ·

A compound represented by Formula (I) is provided:

##STR00001##

In Formula (I), R.sup.3, R.sup.4, and R.sup.5 each independently represent an electron-withdrawing group; R.sup.1, R.sup.2, R.sup.6, and R.sup.7 each independently represent a hydrogen atom, a heterocyclic group, a halogen atom, a nitro group, a cyano group, a hydroxy group, a thiol group, a carboxy group, —SCF.sub.3, —SF.sub.5, —SF.sub.3, —SO.sub.3H, —SO.sub.2H, an aliphatic hydrocarbon group having 1 to 25 carbon atoms which may have a substituent, or an aromatic hydrocarbon group having 6 to 18 carbon atoms which may have a substituent; and R.sup.1 and R.sup.2, R.sup.1 and R.sup.6, R.sup.6 and R.sup.7, and R.sup.4 and R.sup.5 may be linked to each other to form a ring.

COMPOUND

A compound having a molecular weight of 3000 or less and a partial structure represented by Formula (X) is provided:

##STR00001##

In Formula (X), a ring W.sup.1 represents a ring structure having at least one double bond as a constituent element of the ring and having no aromaticity; and R.sup.3 represents a heterocyclic group, a halogen atom, a nitro group, a cyano group, a hydroxy group, a thiol group, a carboxy group, —SF.sub.5, —SF.sub.3, —SO.sub.3H, —SO.sub.2H, an aliphatic hydrocarbon group having 1 to 25 carbon atoms which may have a substituent, or an aromatic hydrocarbon group having 6 to 18 carbon atoms which may have a substituent.

COMPOUND

A compound having a molecular weight of 3000 or less and a partial structure represented by Formula (X) is provided:

##STR00001##

In Formula (X), a ring W.sup.1 represents a ring structure having at least one double bond as a constituent element of the ring and having no aromaticity; and R.sup.3 represents a heterocyclic group, a halogen atom, a nitro group, a cyano group, a hydroxy group, a thiol group, a carboxy group, —SF.sub.5, —SF.sub.3, —SO.sub.3H, —SO.sub.2H, an aliphatic hydrocarbon group having 1 to 25 carbon atoms which may have a substituent, or an aromatic hydrocarbon group having 6 to 18 carbon atoms which may have a substituent.

CIS-PARA-SUBSTITUTED CYCLOHEXYLAMINONITRILE SALT, PREPARATION METHOD THEREFOR AND USE THEREOF, AND METHOD FOR PREPARING PESTICIDE USING SAME

The present application relates to a cis-para-substituted cyclohexylaminonitrile salt represented by formula (I), a preparation method therefor and use thereof as an intermediate for preparing a pesticide, and a method for preparing the pesticide by using same as an intermediate. In the formula, R is C.sub.1-10 alkyl or C.sub.1-10alkyloxy, C.sub.2-10 alkenyl or C.sub.2-10 alkenyloxy, C.sub.2-10 alkynyl or C.sub.2-10 alkynyloxy, C.sub.3-10 cycloalkyl or C.sub.3-10 cycloalkyloxy, C.sub.3-10 heterocycloalkyl or C.sub.3-10 heterocycloalkyloxy containing 1-2 heteroatoms selected from O and N.

##STR00001##

CIS-PARA-SUBSTITUTED CYCLOHEXYLAMINONITRILE SALT, PREPARATION METHOD THEREFOR AND USE THEREOF, AND METHOD FOR PREPARING PESTICIDE USING SAME

The present application relates to a cis-para-substituted cyclohexylaminonitrile salt represented by formula (I), a preparation method therefor and use thereof as an intermediate for preparing a pesticide, and a method for preparing the pesticide by using same as an intermediate. In the formula, R is C.sub.1-10 alkyl or C.sub.1-10alkyloxy, C.sub.2-10 alkenyl or C.sub.2-10 alkenyloxy, C.sub.2-10 alkynyl or C.sub.2-10 alkynyloxy, C.sub.3-10 cycloalkyl or C.sub.3-10 cycloalkyloxy, C.sub.3-10 heterocycloalkyl or C.sub.3-10 heterocycloalkyloxy containing 1-2 heteroatoms selected from O and N.

##STR00001##

CIS-PARA-SUBSTITUTED CYCLOHEXYLAMINONITRILE SALT, PREPARATION METHOD THEREFOR AND USE THEREOF, AND METHOD FOR PREPARING PESTICIDE USING SAME

The present application relates to a cis-para-substituted cyclohexylaminonitrile salt represented by formula (I), a preparation method therefor and use thereof as an intermediate for preparing a pesticide, and a method for preparing the pesticide by using same as an intermediate. In the formula, R is C.sub.1-10 alkyl or C.sub.1-10alkyloxy, C.sub.2-10 alkenyl or C.sub.2-10 alkenyloxy, C.sub.2-10 alkynyl or C.sub.2-10 alkynyloxy, C.sub.3-10 cycloalkyl or C.sub.3-10 cycloalkyloxy, C.sub.3-10 heterocycloalkyl or C.sub.3-10 heterocycloalkyloxy containing 1-2 heteroatoms selected from O and N.

##STR00001##