摘要:
A method for preparing .alpha.-cyano-3-phenoxybenzyl 2-(4-substituted-phenyl)isovalerates which consist substantially of or are rich in the enantiomer pair (S)-.alpha.-cyano-3-phenoxybenzyl (S)-2-(4-substituted-phenyl)isovalerate and (R)-.alpha.-cyano-3-phenoxybenzyl (R)-2-(4-substituted-phenyl)isovalerate.
摘要:
An .alpha.-cyano-3-phenoxybenzyl 2-(4-chlorophenyl)isovalerate which consists substantially of or is rich in (S)-.alpha.-cyano-3-phenoxybenzyl (S)-2-(4-chlorophenyl)isovalerate and (R)-.alpha.-cyano-3-phenoxybenzyl (R)-2-(4-chlorophenyl)isovalerate. A method for preparing the same and an insecticidal and acaricidal composition.
摘要:
An optically active .alpha.-cyano-3-(4-halogenophenoxy)-benzyl 2-(4-chlorophenyl)isovalerate, which consists substantially of or is rich in (S)-.alpha.-cyano-3-(4-halogenophenoxy)benzyl (S)-2-(4-chlorophenyl)isovalerate; a method for preparing the same; and an insecticidal and/or acaricidal composition containing the same.
摘要:
A mixture of stereoisomers of an .alpha.-cyano-3-(4-halogenophenoxy)benzyl 2-(4-chlorophenyl)isovalerate, which consists substantially of or is rich in an enantiomer pair of an (S)-.alpha.-cyano-3-(4-halogenophenoxy)benzyl (S)-2-(4-chlorophenyl)isovalerate and an (R)-.alpha.-cyano-3-(4-halogenophenoxy)benzyl (R)-2-(4-chlorophenyl)isovalerate; a process for preparing the same; and an insecticidal and/or acaricidal composition containing the same.
摘要:
A process for isomerizing optically active .alpha.-cyano-3-phenoxybenzyl 2-(4-chlorophenyl)isovalerate at the asymmetric carbon atom of the 3-phenoxybenzyl moiety, and a process for obtaining (S)-.alpha.-cyano-3-phenoxybenzyl (S)-2-(4-chlorophenyl)isovalerate from (R, S)-.alpha.-cyano-3-phenoxybenzyl (S)-2-(4-chlorophenyl)isovalerate.
摘要:
The present invention relates to a novel method for producing cyclopentenolone of the formula (I), ##STR1## which is a useful intermediate for producing agricultural chemicals, which comprises reacting an acetonedicarboxylic ester of the formula (VII), ##STR2## wherein R is a C.sub.1 -C.sub.6 alkyl group, with 2-propynyl chloride in the presence of magnesium alkoxide and in the presence of alkali iodide to obtain novel mono-(2-propynyl)-substituted acetonedicarboxylic ester of the formula (VI), ##STR3## wherein R is as defined above; hydrolyzing the mono-(2-propynyl)-substituted acetonedicarboxylic ester of the formula (VI) under alkaline conditions with an alkali and then reacting the hydrolyzed product with methylglyoxal of the formula, ##STR4## to obtain novel .gamma.-diketone of the formula (V), ##STR5## and ring-closing the .gamma.-diketone of the formula (V) under alkaline condition.