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
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.
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收藏
页码:3543 / 3546
页数:4
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