AN ENANTIOSPECIFIC ROUTE TO C,D RING SYNTHONS FOR STEROID-SYNTHESIS

被引：25

作者：

CLASE, JA ^{[1
]}

MONEY, T ^{[1
]}

机构：

[1] UNIV BRITISH COLUMBIA,DEPT CHEM,VANCOUVER V6T 1Z1,BC,CANADA

来源：

CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE | 1992年 / 70卷 / 05期

关键词：

D O I：

10.1139/v92-189

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

A simple enantiospecific route to a hydrindenone intermediate for steroid synthesis has been accomplished. The introduction of a wide variety of side-chain units is made possible hy stereoselective alkylation of a bicyclic ester 13 derived from (+)-camphor 4.

引用

页码：1537 / 1544

页数：8

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