EVIDENCE FOR MICHAEL-TYPE REACTION OF ALKENYLIODONIUM SALTS - NUCLEOPHILIC SUBSTITUTIONS WITH SODIUM BENZENESULFINATE

被引：21

作者：

OCHIAI, M ^{[1
]}

KITAGAWA, Y ^{[1
]}

TOYONARI, M ^{[1
]}

UEMURA, K ^{[1
]}

机构：

[1] GIFU PHARMACEUT UNIV,GIFU 502,JAPAN

来源：

TETRAHEDRON LETTERS | 1994年 / 35卷 / 50期

关键词：

D O I：

10.1016/S0040-4039(00)78555-8

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Nucleophilic vinylic substitutions of (Z)-(beta-haloalkenyl)iodonium tetrafluoroborates with sodium benzenesulfinate yielding (Z)-1,2-bis(phenylsulfonyl)alkenes will involve Michael-type addition of the nucleophile to the alkenyliodonium salts at the C-beta atom.

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收藏

页码：9407 / 9408

页数：2

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