THE REACTION OF BETA-AMINOENONES WITH ALPHA-AMINO DERIVATIVES - SYNTHESIS OF 2-FUNCTIONALIZED PYRROLES

被引：17

作者：

ALBEROLA, A

ANDRES, JM

GONZALEZ, A

PEDROSA, R

VICENTE, M

机构：

[1] Departamento de Quimica Organica, Facultad de Ciencias, Universidad de Valladolid. Dr.Mergelina s/n

来源：

HETEROCYCLES | 1990年 / 31卷 / 06期

关键词：

D O I：

10.3987/COM-90-5332

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

β-Aminoenones react with ethyl glycinate, α-aminoacetonitrile and α-aminoacetamide hydrochlorides leading to 2-functionalized pyrroles. Although the transamination is a high-yield process, the transformation of the intermediate, in both basic or thermally induced conditions, affords the corresponding pyrroles in poor to moderate yields. © 1990.

引用

页码：1049 / 1058

页数：10

共 17 条

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