Issue 40, 2022

Heteroarylation of unactivated C–H bonds suitable for late-stage functionalization

Abstract

The late-stage introduction of diverse heterocycles onto complex small molecules enables efficient access to new medicinally relevant compounds. An attractive approach to such a transformation would utilize the ubiquitous aliphatic C–H bonds of a complex substrate. Herein, we report a system that enables direct C–H heteroarylation using a stable, commercially available O-alkenylhydroxamate with heterocyclic sulfone partners. The C–H heteroarylation proceeds efficiently with a range of aliphatic substrates and common heterocycles, and is a rare example of heteroarylation of strong C–H bonds. Importantly, the present approach is amenable to late-stage functionalization as the substrate is the limiting reagent in all cases.

Graphical abstract: Heteroarylation of unactivated C–H bonds suitable for late-stage functionalization

Supplementary files

Article information

Article type
Edge Article
Submitted
17 Aug 2022
Accepted
25 Sep 2022
First published
26 Sep 2022
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY-NC license

Chem. Sci., 2022,13, 11878-11882

Heteroarylation of unactivated C–H bonds suitable for late-stage functionalization

A. S. Miller and E. J. Alexanian, Chem. Sci., 2022, 13, 11878 DOI: 10.1039/D2SC04605A

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