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Electrochemical regioselective methylthiolation of imidazo[2,1-b]thiazoles with DMSO
被引:0
|作者:
Xiao, Meng
[1
]
Yi, Liyu
[1
]
Liu, Wenjie
[1
,2
]
Cao, Gao
[1
,2
]
机构:
[1] Guangdong Pharmaceut Univ, Sch Chem & Chem Engn, Guangzhou, Peoples R China
[2] Guangdong Cosmet Engn & Technol Res Ctr, Guangzhou, Peoples R China
关键词:
DMSO;
electrochemistry;
imidazo[2;
1-b]thiazoles;
methylthiolation;
regioselectivity;
DIMETHYL-SULFOXIDE;
SULFUR;
ACTIVATION;
IMIDAZOPYRIDINES;
THIOMETHYLATION;
SULFENYLATION;
DERIVATIVES;
BENZAMIDES;
AMINATION;
ANTITUMOR;
D O I:
10.1080/00397911.2025.2453872
中图分类号:
O62 [有机化学];
学科分类号:
070303 ;
081704 ;
摘要:
With DMSO both as the source of -SMe unit and solvent, an efficient and green electrochemical methylthiolation reaction of imidazo[2,1-b]thiazoles was developed. The transformation was performed at room temperature in 8 h under external transition metal- and oxidant-free condition. Moreover, the 2,3-dihydroimidazo[2,1-b]thiazoles and 2-phenylbenzo[d]imidazo[2,1-b]thiazole also proceeded smoothly. This strategy provides C-5 methylthiolation products with broad scope in 73-91% yields.
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页码:338 / 349
页数:12
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