电化学铁催化咪唑杂环与氨基甲酸酯的脱氧烷氧羰基化反应

IF 1.8 3区 化学 Q3 CHEMISTRY, ORGANIC
Jun-Qi Zhang , Hangfei Huang , Ying Fu
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引用次数: 0

摘要

咪唑[1,2-a]吡啶衍生物在制药工业和具有生物活性的天然产物中具有广泛的应用。该骨架的多种功能化引起了化学家的广泛关注。本文报道了咪唑杂环在温和无氧化剂条件下,以电子为无痕迹氧化剂的电化学脱氧烷氧羰基化反应。值得注意的是,我们的策略为咪唑[1,2-a]吡啶衍生物引入酯基提供了一种绿色实用的方法,通过使用易于获得且稳定的氨基甲酸酯作为酯源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Electrochemical Fe-catalyzed deoxygenative alkoxycarbonylation of imidazoheterocycles with carbazates
Imidazo[1,2-a]pyridine derivatives possess widespread applications in the pharmaceutical industry and bioactive natural products. The diverse functionalization of this skeleton has attracted much attention from chemists. Herein, we reported an electrochemical deoxygenative alkoxycarbonylation of imidazoheterocycles by using electrons as the traceless oxidant under mild and oxidant-free conditions. Notably, our strategy provided a green and practical approach for introducing ester group into imidazo[1,2-a]pyridine derivatives by employing easily available and bench-stable carbazates as ester source.
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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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