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Stereo‐ and Enantioselective Synthesis of Both cis ‐Chrysanthemic Acid Methyl Esters in High Optical Purity
Author(s) -
FranckNeumann Michel,
Sedrati Madjid,
Vigneron JeanPaul,
Bloy Vincente
Publication year - 1985
Publication title -
angewandte chemie international edition in english
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 0570-0833
DOI - 10.1002/anie.198509961
Subject(s) - enantioselective synthesis , diastereomer , optically active , chemistry , organic chemistry , combinatorial chemistry , stereochemistry , catalysis
The insecticidal activity of pyrethroids depends strongly upon their configuration. A novel synthesis of the highly active title compounds 1 and ent ‐ 1 does not require separation of racemates or diastereomers nor microbiological or enzymatic reactions.
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