CATHODIC COUPLING OF 1, 3, 5-TRI (ARYL AND ALKYLSULFONYL) BENZENES INTO TETRA AND PENTA-SUBSTITUTED BIARYLS

被引：8

作者：

BENASKAR, M ^{[1
]}

SIMONET, J ^{[1
]}

机构：

[1] UNIV RENNES 1,CNRS,ELECTROCHIM ORGAN LAB,F-35042 RENNES,FRANCE

来源：

TETRAHEDRON LETTERS | 1994年 / 35卷 / 11期

关键词：

D O I：

10.1016/0040-4039(94)88330-0

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Tri[aryl and alkylsulfonyl]benzenes cathodically lead in non aqueous conditions to unexpected coupling products either tetra or pentasulfonylbiphenyls depending on the structure of the starting compounds.

引用

页码：1727 / 1730

页数：4

共 6 条

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LAMM, B ;

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[3]

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[4] ELECTROCHEMICAL EVIDENCE FOR AN UNUSUAL BASE-CATALYZED CHAIN MECHANISM IN AN INTRAMOLECULAR HOMOLYTIC ARYLATION [J].

NOVI, M ;

GARBARINO, G ;

DELLERBA, C ;

PETRILLO, G .

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[5]

Patai S., 1988, CHEM SULPHONES SULPH

[6] HOMOGENEOUS ELECTRON-TRANSFER REACTIONS - INCREASED SELECTIVITY IN REDUCTION OF SOME DISULFONES USING INDIRECT ELECTROLYSIS [J].

SIMONET, J ;

LUND, H .

ACTA CHEMICA SCANDINAVICA SERIES B-ORGANIC CHEMISTRY AND BIOCHEMISTRY, 1977, 31 (10) :909-911

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