Amide Synthesis from Decarboxylative Coupling of Isocyanates and Carboxylic Acids

被引:0
作者
Wang, R. [1 ]
Liu, W. H. [1 ]
机构
[1] Sun Yat Sen Univ, Sch Chem, Guangzhou 510006, Peoples R China
基金
中国国家自然科学基金;
关键词
Amide; Carboxylic acid; Isocyanate; Decarboxylation; ACYL AZIDES; CARBON-DIOXIDE; PRIMARY AMINES; CURTIUS REARRANGEMENT; LOSSEN REARRANGEMENT; CONVENIENT REAGENT; HYDROXAMIC ACIDS; FACILE SYNTHESIS; BOND FORMATION; CONVERSION;
D O I
10.1002/cbic.202400770
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Isocyanates are versatile electrophiles that can react with a wide range of nucleophiles to afford important organic structures. Although the reactions between isocyanates and alcohols, amines and organometallic reagents have been well established, the synthesis of amides through the decarboxylative condensation of carboxylic acids and isocyanates is less appreciated. In this review, the synthesis of isocyanates and its application on amide synthesis through the condensation with carboxylic acids are summarized and discussed. It is our hope that this review will attract more attention to this less mentioned transformation and inspire new developments in the fields of organic synthesis, polymer synthesis and chemical biology.
引用
收藏
页数:9
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