The developments of C-N bond formation via electrochemical Ritter-type reactions

被引:2
|
作者
Ma, Yueyue [1 ]
Liu, Caixia [1 ]
Yang, Dali [1 ]
Fang, Ziqi [1 ]
Huang, Wenhui [1 ]
Cheng, Ruihua [1 ]
Ye, Jinxing [1 ]
机构
[1] Guangdong Univ Technol, Sch Biomed & Pharmaceut Sci, Guangzhou 510006, Peoples R China
基金
中国国家自然科学基金;
关键词
ANODIC-OXIDATION; ASYMMETRIC-SYNTHESIS; H AMINATION; ACETONITRILE; AMIDATION; OLEFINS; MILD; CYCLOPROPANES; MEDIATORS; NITRILES;
D O I
10.1039/d4ob01210k
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
With the development of organic electrochemical synthesis, a series of notable achievements have been made in electrochemical Ritter amination reactions, which have enriched the methods available for constructing C-N bonds. In this review, electrochemical Ritter amination reactions are introduced based on the classification of reaction substrates, including olefins, aromatics, alkylbenzenes, and the less reported carboxylic acids, ketones, sulfides, and alkanes. The application of electrochemical technology to Ritter reactions has improved the harsh conditions of the traditional reactions, and extended the substrate scope and the structural diversity of the products. The application value of Ritter reactions in organic synthesis has also been further expanded.
引用
收藏
页码:7537 / 7548
页数:12
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