Institut Charles Gerhardt de Montpellier (ICGM), UMR 5253-CNRS-UM-ENSCM, Ecole Nationale Supérieure de Chimie , 8 rue de l'Ecole Normale, 34296 Montpellier Cedex 5, France.
Chem Rev. 2016 Oct 12;116(19):12029-12122. doi: 10.1021/acs.chemrev.6b00237. Epub 2016 Sep 22.
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 .
本综述概述了非经典(例如,羧酸配体无需预先或原位活化)构建酰胺键的方法。综述的目的是全面讨论相关工作,这些工作主要是在过去 20 年里在该领域完成的。根据底物类别进行数据组织:催化直接从羧酸和胺形成酰胺(第 2 节);羧酸替代物的使用(第 3 节);以及胺替代物的使用(第 4 节)。涉及羧酸和胺替代物的连接策略(NCL、Staudinger、KAHA、KATs 等)在第 5 节中单独处理。