PHEROMONE SYNTHESIS .25. STEREOSELECTIVE SYNTHESIS OF THE BOTH ENANTIOMERS OF DISPARLURE, THE PHEROMONE OF THE GYPSY-MOTH

被引：48

作者：

MORI, K

TAKIGAWA, T

MATSUI, M

机构：

[1] Department of Agricultural Chemistry, The University of Tokyo, Yayoi 1-1-1, Bunkyo-ku

来源：

TETRAHEDRON | 1979年 / 35卷 / 07期

关键词：

D O I：

10.1016/0040-4020(79)80102-7

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

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. © 1979.

引用

页码：833 / 837

页数：5

共 17 条

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