连续流动条件下tfoh催化α-重氮酯合成三组分二硫代氨基甲酸酯

IF 2 4区 化学 Q3 CHEMISTRY, MULTIDISCIPLINARY Journal of Flow Chemistry Pub Date : 2022-12-12 DOI:10.1007/s41981-022-00249-7
Rui Wang, Hangli He, Qiongjiao Yan, Wei Wang, Haifeng Wang, Fener Chen
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引用次数: 1

摘要

二硫代氨基甲酸酯衍生物的合成对其作为药物和其他用途的实际应用具有重要意义。在连续流动条件下,通过α-重氮酯的三组分反应,证明了tfoh催化合成二硫代氨基甲酸酯的良好产率。该反应具有广泛的重氮化合物底物范围和高官能团耐受性。本研究提供了一种安全、温和的合成二硫代氨基甲酸酯的方案,补充了tfoh催化的重氮化合物S-H插入反应和连续流合成策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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TfOH-catalyzed three-component synthesis of Dithiocarbamates from α-Diazoesters under continuous flow conditions

The synthesis of dithiocarbamates derivatives is important for their practical utilization as pharmaceuticals and for other purposes. Herein, we demonstrated the TfOH-catalyzed synthesis of dithiocarbamates via three-component reaction of α-diazoesters in good yields under continuous flow conditions. The reaction exhibits a wide substrate scope of diazo compounds and high functional group tolerance. This study provides a safe and mild protocol to form dithiocarbamates that complements TfOH-catalyzed S-H insertion reaction of diazo compounds and continuous flow synthesis strategies.

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来源期刊
Journal of Flow Chemistry
Journal of Flow Chemistry CHEMISTRY, MULTIDISCIPLINARY-
CiteScore
6.40
自引率
3.70%
发文量
29
审稿时长
>12 weeks
期刊介绍: The main focus of the journal is flow chemistry in inorganic, organic, analytical and process chemistry in the academic research as well as in applied research and development in the pharmaceutical, agrochemical, fine-chemical, petro- chemical, fragrance industry.
期刊最新文献
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