STUDY OF THE REACTION BETWEEN CONJUGATED AZOALKENES AND ALPHA-UNSUBSTITUTED- OR ALPHA-SUBSTITUTED-BETA-DICARBOXYLATE DERIVATIVES - AN IMPROVED PREPARATION OF UNKNOWN POLYFUNCTIONALIZED 1-AMINO-1H-PYRROL-2(3H)-ONES

被引：11

作者：

ATTANASI, OA

DECRESCENTINI, L

SERRAZANETTI, F

FORESTI, E

机构：

[1] UNIV URBINO,FAC SCI,IST CHIM ORGAN,I-61029 URBINO,ITALY

[2] UNIV BOLOGNA,DIPARTIMENTO CHIM G CIAMICIAN,I-40126 BOLOGNA,ITALY

来源：

CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE | 1994年 / 72卷 / 11期

关键词：

D O I：

10.1139/v94-293

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

In the presence of sodium methoxide in catalytic amounts, conjugated azoalkenes easily react with alpha-unsubstituted-or alpha-substituted-beta-dicarboxylate derivatives to give at first hydrazonic derivatives, by 1,4-conjugate addition, and, by increasing sodium methoxide up to stoichiometric amounts, new polyfunctionalized 1-amino-1H-pyrrol-2(3H)-ones.

引用

页码：2305 / 2311

页数：7

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