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通过镍催化的芳基酸酐与噻吩反应形成 C-S 键:脱羰或脱羰伴随脱羧。

Forging C-S Bonds through Nickel-Catalyzed Aryl Anhydrides with Thiophenols: Decarbonylation or Decarbonylation Accompanied by Decarboxylation.

机构信息

College of Pharmaceutical Sciences , Soochow University , Suzhou 215123 , China.

出版信息

J Org Chem. 2019 Sep 20;84(18):11891-11901. doi: 10.1021/acs.joc.9b01746. Epub 2019 Sep 10.

Abstract

A nickel-catalyzed decarbonylation or decarbonylation accompanied by decarboxylation cross-coupling reaction of aryl anhydrides with thiophenols as coupling partners was disclosed. This method is promoted by a commercially available, moisture-stable, and inexpensive nickel(II) precatalyst. The process can tolerate a variety of functional groups using ubiquitous aryl anhydrides as cross-coupling precursors to produce thioethers in moderate to excellent yields.

摘要

一种镍催化的芳基酐与噻酚偶联反应,包括脱羰或脱羰伴随脱羧反应,已被揭示。该方法由一种商业上可获得的、耐湿的、廉价的镍(II)前催化剂促进。该过程可以容忍各种官能团,使用普遍存在的芳基酐作为交叉偶联前体,以中等至优异的收率生成硫醚。

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