95574-44-0Relevant articles and documents
STEREOSELECTIVE SYNTHESIS OF (1R,3S)-CIS-CHRYSANTHEMIC ACID THROUGH MICROBIOLOGICAL REDUCTION OF 2,2,5,5-TETRAMETHYL 1,4-CYCLOHEXANEDIONE.
Buisson, Didier,Azerad, Robert,Revial, Gilbert,d'Angelo, Jean
, p. 6005 - 6006 (1984)
An efficient, highly stereoselective synthesis of (1R,3S)-cis-chrysanthemic acid 6 is described.The crucial step of this synthesis was the microbiological reduction of dione 1 into (S)-ketol 2.
A Short, Efficient, Highly Selective Synthesis of (1R,3S)-cis-Chrysanthemic Acid through the Microbiological Reduction of 2,2,5,5-Tetramethyl-1,4-cyclohexanedione
d'Angelo, Jean,Revial, Gilbert,Azerad, Robert,Buisson, Didier
, p. 40 - 45 (2007/10/02)
A highly selective synthesis of (1R,3S)-cis-chrysanthemic acid (1a), a key intermediate in the industrial prepariation of major unnatural pyrethrinoid-type insecticides is reported. 2,2,5,5-Tetramethyl-1,4-cyclohexanedi