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芳基酮或醛与未活化卤代烃的阴极羰基烷基化反应

Cathodic Carbonyl Alkylation of Aryl Ketones or Aldehydes with Unactivated Alkyl Halides.

作者信息

Wu Hongting, Li Xinling, Yang Ling, Chen Weihao, Zou Canlin, Deng Weijie, Wang Ziliang, Hu Jinhui, Li Yibiao, Huang Yubing

机构信息

School of Biotechnology and Health Sciences, Wuyi University, Jiangmen 529090, P. R. China.

出版信息

Org Lett. 2022 Dec 23;24(50):9342-9347. doi: 10.1021/acs.orglett.2c04019. Epub 2022 Dec 9.

Abstract

An efficient cathodic carbonyl alkylation of aryl ketones or aldehydes with unactivated alkyl halides has been realized through the electrochemical activation of iron. The protocol is believed to include a radical-radical coupling or nucleophilic addition process, and the formation of ketyl radicals and alkyl radicals has been demonstrated. The protocol provides various tertiary or secondary alcohols by the formation of intermolecular C-C bonds under safe and mild conditions, is scalable, consumes little energy, and exhibits a broad substrate scope.

摘要

通过铁的电化学活化实现了芳基酮或醛与未活化卤代烃的高效阴极羰基烷基化反应。该反应历程被认为包括自由基-自由基偶联或亲核加成过程,并且已证实了酮基自由基和烷基自由基的形成。该反应在安全温和的条件下通过分子间C-C键的形成提供了各种叔醇或仲醇,具有可扩展性,能耗低,且底物范围广泛。

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