Amide Bond Formation Strategies: Latest Advances on a Dateless Transformation

被引:201
作者
Massolo, Elisabetta [1 ]
Pirola, Margherita [1 ]
Benaglia, Maurizio [1 ]
机构
[1] Univ Milan, Dipartimento Chim, Via Golgi 19, I-20133 Milan, Italy
关键词
Amidation; Amides; Catalysis; Stoichiometric methods; Synthetic methods; METAL-FREE TRANSAMIDATION; CARBOXYLIC-ACIDS; GREEN CHEMISTRY; AMINO-ACIDS; SECONDARY AMIDES; ALIPHATIC-AMINES; COUPLING REAGENT; DIRECT AMIDATION; DERIVATIVES; CARBOXAMIDES;
D O I
10.1002/ejoc.202000080
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The synthesis of amides remains one of the most important transformations and it is one of the more frequently performed reactions. In the pharmaceutical industry, the formation of the amide group is pivotal and among the more important transformations in the design of the synthetic plan. This review presents an overview of only very recent contributions, published in the last three years, to highlight the latest progress in this "dateless" reaction, with a special focus on metal-free methodologies. New, more efficient and/or greener stoichiometric methods, as well as catalytic strategies, have been discussed, either for the "classic" coupling approach between an amine and a carboxylic acid (or its activated equivalent) or for more innovative approaches, mainly involving oxidation procedures to generate amides starting from amines.
引用
收藏
页码:4641 / 4651
页数:11
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