A SELECTIVE ELECTROCHEMICAL WAY TO FUNCTIONALIZED 6H-1,3-THIAZINES AND OR PYRROLES

被引：7
|
作者：
ABOUELFIDA, A
JUBAULT, M
PRADERE, JP
ROZE, JC
TALLEC, A
机构：
[1] CNRS,URA 475,SYNTH ORGAN LAB,2 RUE HOUSSINIERE,F-44072 NANTES 03,FRANCE
[2] CNRS,URA 439,SYNTH ORGAN & ELECTROCHIM LAB,F-49045 ANGERS,FRANCE
[3] CNRS,URA 439,ELECTROCHIM LAB,F-35042 RENNES,FRANCE
来源：
TETRAHEDRON LETTERS | 1991年 / 32卷 / 20期
关键词：
1-THIA-3-AZA-BUTADIENES; HETERO DIELS-ALDER; ELECTROCHEMICAL REDUCTIONS; 4H-THIAZINES AND 6H-THIAZINES; FUNCTIONALIZED PYRROLES;
D O I：
10.1016/S0040-4039(00)79687-0
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
4H-1,3-thiazines, easily prepared from 1-thia-3-azabutadienes, appear electroactive in protic medium. Controlled potential electroreductions of 4H-1,-3-thiazines lead either to substituted 6H-1,3-thiazines or to pyrroles according to the nature of the C-4 substituent and the acidity of the supporting electrolyte.
引用
收藏
页码：2225 / 2228
页数：4
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