Published in

Wiley, Chinese Journal of Chemistry, 1(30), p. 23-28, 2011

DOI: 10.1002/cjoc.201100482

Links

Tools

Export citation

Search in Google Scholar

Asymmetric Synthesis of Both Enantiomers of Disparlure

Journal article published in 2011 by Wang Zhigang, 黄培强, 郑剑峰, Jianfeng Zheng, Peiqiang Huang ORCID
This paper was not found in any repository; the policy of its publisher is unknown or unclear.
This paper was not found in any repository; the policy of its publisher is unknown or unclear.

Full text: Unavailable

Green circle
Preprint: archiving allowed
Orange circle
Postprint: archiving restricted
Red circle
Published version: archiving forbidden
Data provided by SHERPA/RoMEO

Abstract

Starting from propargyl alcohol (12), and on the basis of Zhou's modified Sharpless asymmetric epoxidation, the sex pheromone of the Gypsy moth, disparlure (+)-8 and its enantiomer (-)-8 have been synthesized, each in six steps, with overall yields of 29% for (+)-8 and 27% for (-)-8 (ee>98%). The use of the sequential coupling tactic renders the method flexible, which is applicable to the synthesis of other cis-epoxy pheromones. ; National Basic Research Program (973 Program) of China [2010CB833200]; National Natural Science Foundation of China [20832005]; Natural Science Foundation of Fujian Province of China [2011J01054]