Radical cyclization of allyl α-bromocarboxylates into λ-butyrolactones. Effect of the ester structure on the cyclization

被引：0
|
作者：
A. B. Terent'ev
T. T. Vasil'eva
N. A. Kuz'mina
N. S. Ikonnikov
S. A. Orlova
E. I. Mysov
Yu. N. Belokon'
机构：
[1] Russian Academy of Sciences,A. N. Nesmeyanov Institute of Organoelement Compounds
来源：
Russian Chemical Bulletin | 1997年 / 46卷
关键词：
cyclization; ally esters; bromocarboxylic acids; iron pentacarbonyl; radicals;
D O I：
暂无
中图分类号：
学科分类号：
摘要：
Allyl dibromoacetate, allyl α-bromopropionate, and allyl phenylbromoacetate undergo cyclization in benzene in the presence of increased concentration of Fe(CO)5—DMF as the initiating system to give the corresponding bromo-substituted butyrolactones.
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页码：2096 / 2098
页数：2
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