Preparation of useful synthetic intermediates of taxol analogs, cyclooctenone derivatives

被引:0
|
作者
Yamada, K [1 ]
Tozawa, T [1 ]
Saitoh, K [1 ]
Mukaiyama, T [1 ]
机构
[1] Sci Univ Tokyo, Fac Sci, Dept Appl Chem, Shinjuku Ku, Tokyo 162, Japan
关键词
cyclooctenone; samarium(II) iodide; omega-(alpha-bromoketo) aldehyde; deoxygenated taxane framework;
D O I
暂无
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Stereoselective syntheses of omega-(alpha-bromoketo) octanals and nonanal with oxygenated functions and formation of the corresponding eight-membered carbocyclic aldols by subsequent samarium(II)-mediated cyclization are demonstrated. Cyclooctenones deoxygenated at the C2 or C10 position in the taxane framework are prepared by dehydration of the above aldols.
引用
收藏
页码:2113 / 2115
页数:3
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