Benzylic intermolecular carbon-carbon bond formation by selective anodic oxidation of dithioacetals

被引：35

作者：

Chiba, K ^{[1
]}

Uchiyama, R ^{[1
]}

Kim, S ^{[1
]}

Kitano, Y ^{[1
]}

Tada, M ^{[1
]}

机构：

[1] Tokyo Univ Agr & Technol, Bioorgan Chem Lab, Fuchu, Tokyo 1838509, Japan

来源：

ORGANIC LETTERS | 2001年 / 3卷 / 08期

关键词：

D O I：

10.1021/ol015734a

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Novel anodic intermolecular carbon-carbon bond formation has been accomplished by the oxidative carbon-sulfur bond fission of benzylic dithioacetals to give a wide variety of aromatic compounds. The substitution reaction successfully took place by the selective anodic oxidation of a sulfur atom of a dithioacetal. Stepwise double-substitution reactions were also achieved by the regulation of oxidation potential.

引用

页码：1245 / 1248

页数：4

共 30 条

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