N,N,N',N'-Tetramethylethylenediamine-Enabled PhotoredoxCatalyzed C-H Methylation of N-Heteroarenes

被引:20
|
作者
Liu, Fang [1 ]
Ye, Zhi-Peng [1 ]
Hu, Yuan-Zhuo [1 ]
Gao, Jie [1 ]
Zheng, Lan [1 ]
Chen, Kai [1 ,2 ]
Xiang, Hao-Yue [1 ]
Chen, Xiao-Qing [1 ,3 ]
Yang, Hua [1 ,3 ]
机构
[1] Cent South Univ, Coll Chem & Chem Engn, Changsha 410083, Peoples R China
[2] Peking Univ, Key Lab Chem Oncogen, Shenzhen Grad Sch, Shenzhen 518055, Peoples R China
[3] Cent South Univ, Key Lab Hunan Prov Water Environm & Agr Prod Safe, Changsha 410083, Peoples R China
基金
中国国家自然科学基金;
关键词
PHOTOINDUCED METHYLATION; CATALYZED METHYLATION; CARBOXYLIC-ACIDS; DNA METHYLATION; OXIDATION; ALKYLATION; QUINOXALIN-2(1H)-ONES; PEROXIDE; CLEAVAGE; DERIVATIVES;
D O I
10.1021/acs.joc.1c01325
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Aiming at the valuable methylation process, readily available and inexpensive N, N, N', N'- tetramethylethylenediamine (TMEDA) was first identified as a new methyl source in photoredox-catalyzed transformation in this work. By virtue of this simple methylating reagent, a facile and practical protocol for the direct C-H methylation of N-heteroarenes was developed, featuring mild reaction conditions, broad substrate scope, and scalability. Mechanistic studies disclosed that a sequential photoredox, base-assisted proton shift, fragmentation, and tautomerization process was essentially involved.
引用
收藏
页码:11905 / 11914
页数:10
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