CATALYST-FREE SYNTHESIS OF α-AMINOACYL-AMIDES VIA N,N′-BIS(PHENYLMETHYLIDENE)PHENYLMETHANEDIAMINE AS IMINE SURROGATE IN UGI MULTICOMPONENT REACTION

被引：7

作者：

Alizadeh, Abdolali ^{[1
]}

Mokhtari, Javad ^{[1
]}

机构：

[1] Tarbiat Modares Univ, Dept Chem, Tehran, Iran

来源：

SYNTHETIC COMMUNICATIONS | 2012年 / 42卷 / 05期

关键词：

Diimine; isocyanide; three-component reaction; Ugi reaction; AROMATIC-ALDEHYDES; DERIVATIVES; CHEMISTRY;

D O I：

10.1080/00397911.2010.529229

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

A novel one-pot, multicomponent, and catalyst-free reaction of N,N'-bis(phenylmethylidene)phenylmethane, carboxylic acids, and isocyanides yielding alpha-aminoacyl-amides is described. The reaction is based on the combination of an Ugi three-component reaction followed by hydrolysis.

引用

收藏

页码：686 / 693

页数：8

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