PHEROMONE SYNTHESIS .29. STEREOCONTROLLED SYNTHESIS OF ALL OF THE 4 POSSIBLE STEREOISOMERS OF ERYTHRO-3,7-DIMETHYLPENTADEC-2-YL ACETATE AND PROPIONATE, THE SEX-PHEROMONE OF THE PINE SAWFLIES

被引:74
作者
MORI, K
TAMADA, S
机构
[1] Department of Agricultural Chemistry, The University of Tokyo, Bunkyo-ku, Tokyo, 113
关键词
D O I
10.1016/0040-4020(79)80054-X
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
All of the four possible stereoisomers of 2,3-erythro-3,7-dimethylpentadecan-2-ol 1 were synthesized by a stereospecific SN2 oxirane cleavage of (2S,3S)-2,3-epoxybutane or its antipode with lithium di[(R)- or (S)-4-methyldodecyl]cuprate. Their acetates or propionates were prepared to test their pheromone activity. © 1979.
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页码:1279 / 1284
页数:6
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