A STEREOSPECIFIC ROUTE TO FUNCTIONALIZED ALKENES FROM TETRAHYDROFURFURYLIC ACETATES - SYNTHESIS OF PHEROMONES

被引：12

作者：

AMOUROUX, R

EJJIYAR, S

机构：

[1] Laboratoire de Chimie Organique Physique, associé au CNRS, Université Claude Bernard, 69622 VILLEURBANNE -, 43 Boulevard du

来源：

TETRAHEDRON LETTERS | 1991年 / 32卷 / 26期

关键词：

D O I：

10.1016/0040-4039(91)80688-3

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Pure Z or E gamma-iodoalkenes were prepared by a ring opening-elimination tandem reaction of erythro or threo secondary tetrahydrofurfurylic acetates with Me3SiCl/NaI. Applications to the synthesis of pheromones of Musca domestica and of Orgyia pseudotsugata are reported.

引用

页码：3059 / 3062

页数：4

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