RADICAL CYCLIZATION OF DIENES AND ENYNES USING TOLSO2SEPH

被引：25

作者：

BRUMWELL, JE

SIMPKINS, NS

TERRETT, NK

机构：

[1] UNIV NOTTINGHAM,DEPT CHEM,UNIV PK,NOTTINGHAM NG7 2RD,ENGLAND

[2] PFIZER LTD,SANDWICH CT13 9NJ,KENT,ENGLAND

来源：

TETRAHEDRON LETTERS | 1993年 / 34卷 / 07期

关键词：

D O I：

10.1016/S0040-4039(00)77533-2

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Reaction of a number of 1,6-diene or enyne systems with TolSO2SePh, under free radical conditions, results in selenosulphonylation with concommitant C-C bond formation, to give cyclised alkyl or vinyl sulphones containing the synthetically useful phenylselenyl functionality.

引用

页码：1219 / 1222

页数：4

共 12 条

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[8] SYNTHESIS OF N-PROTECTED SPIROAMINES RELATED TO NATURAL-PRODUCTS USING RADICAL CYCLIZATIONS
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