Stereoselective synthesis of the both enantiomers of disparlure, the pheromone of the gypsy moth
作者:K. Mori、T. Takigawa、M. Matsui
DOI:10.1016/0040-4020(79)80102-7
日期:——
The both enantiomers of disparlure [(7R, 8S)-(+)-epoxy-2-methyloctadecane and its (7S,8R)-(−)-isomer] were synthesized from (2R, 3R)-(+)-tartaric acid in a stereoselective manner. (+)-Disparlure was found to be biologically active.