Metal-Free Electrochemical C―H Chlorination of Terminal Alkanes

被引:0
|
作者
Wang, Qingxu [1 ]
Fang, Pengkai [1 ]
Zhao, Jianyou [1 ]
Huang, Xianting [1 ]
Shen, Xiaoqian [1 ]
Wang, Fan [1 ]
Liu, Zhong-Quan [1 ]
机构
[1] Nanjing Univ Chinese Med, Coll Pharm, Jiangsu Collaborat Innovat Ctr Chinese Med Resourc, Nanjing 210023, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
C & horbar; H functionalization; Electrochemistry; Free radicals; Halogenation; Late-stage functionalization; C-H BONDS; C(SP(3))-H BORYLATION; FUNCTIONALIZATION; HYDROXYPHTHALIMIDE; ACTIVATION; CHEMISTRY; OXIDATION;
D O I
10.1002/anie.202504478
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Although research on the activation of C & horbar;H bonds in alkanes has been ongoing for decades, there are still few strategies that are both highly selective and suitable for industrial production. Herein, we report a highly selective method for the chlorination of terminal C & horbar;H bonds in alkanes by combining electrochemistry and organocatalysis. The specific cavity size of organic molecular catalysts ensures high regioselectivity, while the use of inexpensive and readily reusable graphite felt electrodes, a simple electrochemical device, and mild conditions enables the reaction to maintain good efficiency even when applied to kilogram-scale production.
引用
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页数:8
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