Enantioselective total synthesis of δ-lactonic marine natural products, (+)-tanikolide and (-)-malyngolide, via RCM reaction

被引：52
作者：
Mizutani, H [1 ]
Watanabe, M [1 ]
Honda, T [1 ]
机构：
[1] Hoshi Univ, Fac Pharmaceut Sci, Shinagawa Ku, Tokyo 1428501, Japan
来源：
TETRAHEDRON | 2002年 / 58卷 / 44期
关键词：
ring-closing metathesis; (+)-tanikolide; (-)-malyngolide; marine natural product; lactonic compound;
D O I：
10.1016/S0040-4020(02)01160-2
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
Enantioselective total synthesis of delta-lactonic marine natural products, (+)-tanikolide and (-)-malyngolide isolated from Lyngbya majuscula, was achieved by using the Sharpless asymmetric epoxidation and a ring-closing metathesis, as key reactions. (C) 2002 Elsevier Science Ltd. All rights reserved.
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收藏
页码：8929 / 8936
页数：8
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