CO Insertion Enabled γ-C(sp3)-H Heteroarylative Carbonylation of Tertiary Alcohols via Heteroaryl Migration

Abstract

The direct functionalization of remote C(sp3)-H is valuable but challenging, which is even more difficult to achieve the γ-C(sp3)-H functionalization of alcohols. Among the strategies, hydrogen atom transfer (HAT) is one of the solutions for such transformations. Herein, we designed a migration reaction involving carbon monoxide, forming alkoxy radical by photocatalysis, and used carbon monoxide to extend the carbon chain to provide a site for the migration of heteroaryl groups, which makes 1,4-HAT more advantageous, and relied on this strategy to successfully achieve the synthesis of 1,4-dicarbonyl compounds by γ-C(sp3) functionalization of alcohols.

Supplementary files

Article information

Article type
Communication
Submitted
10 Okt. 2024
Accepted
04 Nov. 2024
First published
04 Nov. 2024
This article is Open Access
Creative Commons BY license

Chem. Commun., 2024, Accepted Manuscript

CO Insertion Enabled γ-C(sp3)-H Heteroarylative Carbonylation of Tertiary Alcohols via Heteroaryl Migration

X. Qi, Y. Wang and X. Wu, Chem. Commun., 2024, Accepted Manuscript , DOI: 10.1039/D4CC05361C

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