Electrochemical Oxidative C-H Amination of Phenols: Access to Triarylamine Derivatives

被引:155
作者
Tang, Shan [1 ]
Wang, Siyuan [1 ]
Liu, Yichang [1 ]
Cong, Hengjiang [1 ]
Lei, Aiwen [1 ,2 ]
机构
[1] Wuhan Univ, Coll Chem & Mol Sci, IAS, Wuhan 430072, Hubei, Peoples R China
[2] Chinese Acad Sci, Lanzhou Inst Chem Phys, State Key Lab Oxo Synth & Select Oxidat, Lanzhou 730000, Gansu, Peoples R China
基金
中国国家自然科学基金;
关键词
amination; C-H functionalization; cross-coupling; electrochemistry; heterocyles; TRANSFER RADICAL POLYMERIZATION; CROSS-COUPLING REACTIONS; N BOND FORMATION; MOLECULAR MATERIALS; FUNCTIONALIZATION; OXIDANT; CATALYSIS; ARENES; ANNULATION; DEVICES;
D O I
10.1002/anie.201800240
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Dehydrogenative C-H/N-H cross-coupling serves as one of the most straightforward and atom-economical approaches for C-N bond formation. In this work, an electrochemical reaction protocol has been developed for the oxidative C-H amination of unprotected phenols under undivided electrolytic conditions. Neither metal catalysts nor chemical oxidants are needed to facilitate the dehydrogenation process. A series of triarylamine derivatives could be obtained with good functional-group tolerance. The electrolysis is scalable and can be performed at ambient conditions.
引用
收藏
页码:4737 / 4741
页数:5
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