Synthesis of the C1-C12 fragment of the tedanolides.: Aldol-non-aldol aldol approach

被引：18

作者：

Jung, Michael E. ^{[1
]}

Yoo, Dongwon ^{[1
]}

机构：

[1] Univ Calif Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90095 USA

来源：

ORGANIC LETTERS | 2007年 / 9卷 / 18期

关键词：

D O I：

10.1021/ol0714038

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The combination of highly stereoselective non-aldol aldol and aldol processes allows the preparation of the completely protected C-1-C-12 fragment 2 of the novel macrocyclic cytotoxic agent tedanolide 1.

引用

页码：3543 / 3546

页数：4

共 31 条

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