DICHOTOMY IN THE ADDITION OF CARBON-CENTERED RADICALS TO KETENEDITHIOACETALS

被引：17

作者：

HARROWVEN, DC

BROWNE, R

机构：

来源：

TETRAHEDRON LETTERS | 1994年 / 35卷 / 29期

关键词：

D O I：

10.1016/S0040-4039(00)77090-0

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Further studies on the addition of carbon centred radicals to ketenedithioacetals have shown that cyclisation may occur to either the sulfur atom or the alkene moiety and that the outcome is governed by the availability of a 5-exo cyclisation process.

引用

页码：5301 / 5302

页数：2

共 5 条

[1]

Curran D. P., 1991, COMPREHENSIVE ORGANI, V4, P779

[2] CASCADE RADICAL REACTIONS IN SYNTHESIS - CONDENSED THIOPHENES FROM KETENETHIOACETALS [J].