THIOSILANES IN ORGANIC-SYNTHESIS - A NOVEL-APPROACH TO VINYL SULFIDES

被引：0
|
作者：
DEGL'INNOCENTI, A
ULIVI, P
CAPPERUCCI, A
MORDINI, A
REGINATO, G
RICCI, A
机构：
[1] DIPARTIMENTO CHIM ORGAN, I-50121 FLORENCE, ITALY
[2] UNIV BOLOGNA, DIPARTIMENTO CHIM ORGAN A MANGINI, I-40136 BOLOGNA, ITALY
来源：
SYNLETT | 1992年 / 06期
关键词：
D O I：
暂无
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
Silyl enol ethers 1 react under the influence of diethyl ether-boron trifluoride complex with silylated sulphides to afford a new and general access to a wide range of vinyl sulphides 2. When alpha,beta-unsaturated ketones are used, a mild synthesis of 1,3-bis(phenylthio)propenes 6 is achieved.
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页码：499 / 501
页数：3
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