First diastereoselective chiral synthesis of (-)-securinine

被引：119

作者：

Honda, T ^{[1
]}

Namiki, H ^{[1
]}

Kaneda, K ^{[1
]}

Mizutani, H ^{[1
]}

机构：

[1] Hoshi Univ, Fac Pharmaceut Sci, Shinagawa Ku, Tokyo 1428501, Japan

来源：

ORGANIC LETTERS | 2004年 / 6卷 / 01期

关键词：

D O I：

10.1021/ol0361251

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

A diastereoselective total synthesis of securinine in optically pure form was achieved by employing ring-closing metathesis of the corresponding dienyne compound as a key step.

引用

页码：87 / 89

页数：3

共 31 条

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