INDOLYL PARTICIPATION IN THE MITSUNOBU REACTION - RETENTION OF STEREOCHEMISTRY

被引：13

作者：

AUDIA, JE

COLOCCI, N

机构：

[1] Lilly Research Laboratories, Eli Lilly and Co., Indianapolis

来源：

TETRAHEDRON LETTERS | 1991年 / 32卷 / 31期

关键词：

D O I：

10.1016/S0040-4039(00)79374-9

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The Mitsunobu reaction of trans-3-(2-hydroxycyclohexyl)indole with phthalimide results in the formation of trans-3-(2-N-phthalimidocyclohexyl)indole, presumably via indolyl participation in the displacement reaction. Involvement of symmetrical intermediate 7 is evidenced by deuterium label scrambling.

引用

页码：3779 / 3782

页数：4

共 13 条

[1] ELECTROPHILIC SUBSTITUTION IN INDOLES .V. INDOLENINES AS INTERMEDIATES IN BENZYLATION OF 3-SUBSTITUTED INDOLES [J].