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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.

SUBMITTER: Miller AS 

PROVIDER: S-EPMC9580477 | biostudies-literature | 2022 Oct

REPOSITORIES: biostudies-literature

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

Miller Austin S AS   Alexanian Erik J EJ  

Chemical science 20220926 40


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 <i>O</i>-alkenylhydroxamate with heterocyclic sulfone partners. The C-H heteroarylation proceeds efficiently with a range of ali  ...[more]

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