The effect of topologically controlled coulombic interactions on the regioselectivity of the reductive cleavage of alkyl phenyl ethers

被引:13
作者
Azzena, U
Casado, F
Fois, P
Gallardo, I
Pisano, L
Marquet, J
Melloni, G
机构
[1] UNIV AUTONOMA BARCELONA, DEPT QUIM, BELLATERRA 08193, BARCELONA, SPAIN
[2] UNIV SASSARI, DIPARTIMENTO CHIM, I-07100 SASSARI, ITALY
来源
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2 | 1996年 / 12期
关键词
D O I
10.1039/p29960002563
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The importance of electrostatic effects in the chemical evolution of charged intermediates of the radical anion type is demonstrated, Thus, the regioselectivity of the electron transfer-induced reductive cleavage of alkyl 2,6-diphenylphenyl ethers and alkyl 2,6-dimethoxyphenyl ethers is completely reversed when a positive charge is placed in a controlled manner near the alkyl ether bond.
引用
收藏
页码:2563 / 2565
页数:3
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