Nonclassical Routes for Amide Bond Formation

被引：811

作者：

de Figueiredo, Renata Marcia ^{[1
]}

Suppo, Jean-Simon ^{[1
]}

Campagne, Jean-Marc ^{[1
]}

机构：

[1] Ecole Natl Super Chim, ICGM, UMR 5253, CNRS,UM,ENSCM, 8 Rue Ecole Normale, F-34296 Montpellier 5, France

来源：

CHEMICAL REVIEWS | 2016年 / 116卷 / 19期

关键词：

NATIVE CHEMICAL LIGATION; SOLID-PHASE SYNTHESIS; CATALYZED OXIDATIVE AMIDATION; TRACELESS STAUDINGER LIGATION; FMOC-BASED SYNTHESIS; C-H ACTIVATION; INTRAMOLECULAR ACYL TRANSFER; AMINE CAPTURE STRATEGY; PRIOR THIOL CAPTURE; ONE-POT SYNTHESIS;

D O I：

10.1021/acs.chemrev.6b00237

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

The present review offers an overview of nonclassical (e.g., with no pre-or in situ activation of a carboxylic acid partner) approaches for the construction of amide bonds. The review aims to comprehensively discuss relevant work, which was mainly done in the field in the last 20 years. Organization of the data follows a subdivision according to substrate classes: catalytic direct formation of amides from carboxylic and amines (section 2 ); the use of carboxylic acid surrogates (section 3); and the use of amine surrogates (section 4). The ligation strategies (NCL, Staudinger, KAHA, KATs, etc.) that could involve both carboxylic acid and amine surrogates are treated separately in section 5 .

引用

页码：12029 / 12122

页数：94

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