咪唑[2,1-b]噻唑与DMSO的电化学区域选择性甲基硫化

IF 1.8 3区 化学 Q3 CHEMISTRY, ORGANIC
Meng Xiao , Liyu Yi , Wenjie Liu , Gao Cao
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引用次数: 0

摘要

以DMSO为-SMe单元源和溶剂,建立了咪唑[2,1-b]噻唑的高效、绿色电化学甲基硫化反应。在室温下,在外部过渡金属和无氧化剂的条件下,在8 h内进行转变。此外,2,3-二氢咪唑[2,1-b]噻唑和2-苯基苯并[d]咪唑[2,1-b]噻唑也进行顺利。该策略提供了广泛的C-5甲基硫代化产品,收率为73-91%。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Electrochemical regioselective methylthiolation of imidazo[2,1-b]thiazoles with DMSO
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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来源期刊
Synthetic Communications
Synthetic Communications 化学-有机化学
CiteScore
4.40
自引率
4.80%
发文量
156
审稿时长
4.3 months
期刊介绍: Synthetic Communications presents communications describing new methods, reagents, and other synthetic work pertaining to organic chemistry with sufficient experimental detail to permit reported reactions to be repeated by a chemist reasonably skilled in the art. In addition, the Journal features short, focused review articles discussing topics within its remit of synthetic organic chemistry.
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