THE CYCLODIMERIZATION OF ARYL VINYL SULFONES - A FACILE AND SPECIFIC REACTION WHEN ACTIVATED BY CATHODIC ELECTRON-TRANSFER

被引：41

作者：

DELAUNAY, J ^{[1
]}

MABON, G ^{[1
]}

ORLIAC, A ^{[1
]}

SIMONET, J ^{[1
]}

机构：

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

来源：

TETRAHEDRON LETTERS | 1990年 / 31卷 / 05期

关键词：

D O I：

10.1016/S0040-4039(00)94597-0

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Aryl vinyl sulphones, when "reduced" under well defined experimental conditions, do not lead to cleavage products or to hydrodimers but to cyclodimers, namely trans bis-1,2-(aryl sulphonyl)-cyclobutanes. © 1990.

引用

页码：667 / 668

页数：2

共 6 条

[1]

Baizer M.M., 1983, ORGANIC ELECTROCHEMI

[2] ON THE UNEXPECTED CATHODIC ELECTRODIMERIZATION OF PHENYL VINYL SULFONE IN SLIGHTLY PROTIC MEDIA - THE FORMATION OF 1,4-BISPHENYLSULPHONYLBUT-2-ENE [J].

DJEGHIDJEGH, N ;

SIMONET, J .

JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1988, (19) :1317-1318

[3]

DJEGHIDJEGH N, 1988, THESIS U RENNES 1

[4]

ELFAGHI MS, 1981, J ORG CHEM, V46, P4258

[5]

ELFAGHI MSE, 1981, NOUV J CHIM, V5, P251

[6]

SIMONET J, 1983, CHEM SULPHONES SULPH

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