THIANICKELACYCLES BY RING-OPENING REACTIONS OF CYCLIC THIOETHERS AND THEIR SUBSEQUENT CARBONYLATION TO THIOESTERS

被引:46
作者
MATSUNAGA, PT [1 ]
HILLHOUSE, GL [1 ]
机构
[1] UNIV CHICAGO,DEPT CHEM,SEARLE CHEM LAB,CHICAGO,IL 60637
来源
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH | 1994年 / 33卷 / 17期
关键词
D O I
10.1002/anie.199417481
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A functional model for the nickel‐containing CO‐dehydrogenase? Oxidative addition reactions of ethylene sulfide, propylene sulfide, and thietane with nickel complexes like 1 yield thianickelacycles. Formally analogous to the biosynthesis of acetyl coenzyme A, 2 undergoes an insertion reaction with CO followed by reductive elimination of the thiobutyrolactone 3. (Figure Presented.) Copyright © 1994 by VCH Verlagsgesellschaft mbH, Germany
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页码:1748 / 1749
页数:2
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