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通过空气中的催化碘由芳基肼生成芳基自由基:取代的1,4-萘醌的芳基化反应

Generation of Aryl Radicals from Aryl Hydrazines via Catalytic Iodine in Air: Arylation of Substituted 1,4-Naphthoquinones.

作者信息

Sar Saibal, Chauhan Jyoti, Sen Subhabrata

机构信息

Department of Chemistry, School of Natural Sciences, Shiv Nadar University, Dadri, Chithera, Gautam Budh Nagar, Uttar Pradesh 201314, India.

出版信息

ACS Omega. 2020 Feb 21;5(8):4213-4222. doi: 10.1021/acsomega.9b04014. eCollection 2020 Mar 3.

Abstract

Arylated building blocks or heterocycles are key to myriad applications, including pharmaceutical drug discovery, materials sciences, and many more. Herein, we have reported a mild and efficient strategy for generation of aryl radicals by reacting appropriate aryl hydrazines with catalytic iodine in open air. The aryl radicals were quenched by diversely substituted 1,4-napthoquinones present in the reaction mixture to afford diversely substituted 2,3-napthoquinones in moderate to excellent yield. Control experiments provided insights into the putative reaction mechanism.

摘要

芳基化结构单元或杂环化合物是众多应用的关键,包括药物研发、材料科学等等。在此,我们报道了一种温和且高效的策略,即在空气中使合适的芳基肼与催化量的碘反应来生成芳基自由基。反应混合物中存在的不同取代的1,4-萘醌淬灭芳基自由基,从而以中等至优异的产率得到不同取代的2,3-萘醌。对照实验为推测的反应机理提供了见解。

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