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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.
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页码:11905 / 11914
页数:10
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