Electrochemical N(sp2)-H/C(sp3)-H cross-coupling reaction between sulfoximines and alkylarenes

被引:9
|
作者
Zhu, Qing-Ru [1 ]
Zhang, Peng-Zhan [1 ]
Sun, Xiang [1 ]
Gao, Hui [1 ]
Wang, Pei-Long [1 ]
Li, Hongji [1 ]
机构
[1] Huaibei Normal Univ, Sch Chem & Mat Sci, Minist Educ, Key Lab Green & Precise Synthet Chem & Applicat, Huaibei 235000, Anhui, Peoples R China
基金
中国国家自然科学基金; 美国国家科学基金会;
关键词
C-H FUNCTIONALIZATION; PRIMARY AMINES; AMMONIA; ALKYLATION; ELECTROSYNTHESIS; METHYLARENES; OXYGENATION; AMINATION; EFFICIENT; ALCOHOLS;
D O I
10.1039/d4gc00191e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
An electrochemical oxidation-induced amination of simple alkylarenes with sulfoximines as a nitrogen source and 5,6-dimethyl-1H-benzo[d]imidazole as a catalyst under mild conditions was developed. This protocol represents a rare example of benzylic C-H functionalization of alkylarenes that involves the electrochemical generation of N-center radical, providing access to a range of corresponding aminated products in moderate to good yields.
引用
收藏
页码:5824 / 5831
页数:8
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