Electrochemical/Photochemical Aminations Based on Oxidative Cross-Coupling between C-H and N-H

被引:36
|
作者
Zhang, Heng [1 ]
Lei, Aiwen [1 ,2 ,3 ]
机构
[1] Wuhan Univ, Coll Chem & Mol Sci, Wuhan 430072, Hubei, Peoples R China
[2] Nankai Univ, State Key Lab, Tianjin 300071, Peoples R China
[3] Nankai Univ, Inst Elementoorgan Chem, Tianjin 300071, Peoples R China
来源
SYNTHESIS-STUTTGART | 2019年 / 51卷 / 01期
基金
中国国家自然科学基金;
关键词
oxidative cross coupling; amination; C-H bond functionalization; electrochemistry; photochemistry; VISIBLE-LIGHT PHOTOREDOX; HYDROGEN EVOLUTION REACTION; FUNCTIONALIZATION; ARENES; IODINE; AZOLES; ARYL; SULFONIMIDES; HETEROARENES; HYDROCARBONS;
D O I
10.1055/s-0037-1610380
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The construction of nitrogen-containing molecules remains at the cutting edge of organic synthesis because of its wide application in various areas. Instead of prefunctionalized substrates, using free C-H and N-H bonds in the starting materials can supply a more sustainable avenue to the C-N bond-forming reactions. Compared with the well-developed transition-metal-catalyzed protocols, the strategy of introducing optical or electrical energy into reactions is fantastic and appealing. As a result, visible light or electricity mediated amination transformations have continued to develop over the past several years. In this short review, recent progress of carbon-nitrogen bond-forming reactions based on the oxidative cross coupling between C(sp(2), sp(3))-H and N-H are summarized.
引用
收藏
页码:83 / 96
页数:14
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