ELECTROCHEMICAL TRIFLUOROMETHYLATION OF OLEFINS - PRODUCT-SELECTIVITY AND MECHANISTIC ASPECTS

被引:42
作者
UNEYAMA, K
机构
[1] Department of Applied Chemistry, Faculty of Engineering, Okayama University, Okayama
关键词
D O I
10.1016/S0040-4020(01)87045-9
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Trifluoroacetic acid (TFA) can be converted almost quantitatively to the trifluoromethyl radicals by electrochemical oxidation of TFA. The electrolysis is conducted in an MeCN-H2O-(Pt) system using an undivided cell. The electrochemically generated CF3.radicals can attack mostly electron-deficient olefins leading to the trifluoromethylated carbon radicals of which chemical and electrochemical fate can be controlled by current density, reaction temperature, and substituents of olefins.
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页码:555 / 562
页数:8
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