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镍催化杂芳基溴化物与叔卤代烃的还原偶联反应。

Ni-Catalyzed Reductive Coupling of Heteroaryl Bromides with Tertiary Alkyl Halides.

机构信息

School of Materials Science and Engineering, Shanghai University, 99 Shang-Da Road, Shanghai 200444, China.

Center for Supramolecular Chemistry and Catalysis, Department of Chemistry, Shanghai University, 99 Shang-Da Road, Shanghai 200444, China.

出版信息

Org Lett. 2022 Dec 16;24(49):8996-9000. doi: 10.1021/acs.orglett.2c03598. Epub 2022 Dec 1.

Abstract

We disclose here a nickel-catalyzed reductive coupling of bromopyridines with tertiary alkyl bromides for the synthesis of alkylated pyridines bearing an all-carbon quaternary center. This strategy features mild conditions, broad substrate scope, and high functional group tolerance. The method reported here offers an alternative solution to the challenging task of forging sterically congested alkylpyridines, which we believe will significantly benefit the synthetic community and pharmaceutical industry.

摘要

我们在此披露了一种镍催化的溴代吡啶与叔烷基溴的还原偶联反应,用于合成含有全碳季碳中心的烷基化吡啶。该策略具有条件温和、底物范围广、官能团容忍度高的特点。本文报道的方法为构建空间位阻较大的烷基吡啶这一具有挑战性的任务提供了一种替代方案,我们相信这将极大地有益于合成界和制药行业。

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