Radical cyclization of O-trityl oximino esters:: a ring closure that preserves the oxime function

被引：18

作者：

Clive, DLJ ^{[1
]}

Subedi, R ^{[1
]}

机构：

[1] Univ Alberta, Dept Chem, Edmonton, AB T6G 2G2, Canada

来源：

CHEMICAL COMMUNICATIONS | 2000年 / 03期

关键词：

D O I：

10.1039/a908842c

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

O-Trityl oximino esters 1 undergo stannane-induced radical cyclization to regenerate an oxime function, affording oximino lactones 4; these can be converted into enamides (e.g. 11b), and such a transformation was used to make the natural product 14c.

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页码：237 / 238

页数：2

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