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

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 en...

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Detalles Bibliográficos
Autores principales: Miller, Austin S., Alexanian, Erik J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9580477/
https://www.ncbi.nlm.nih.gov/pubmed/36320922
http://dx.doi.org/10.1039/d2sc04605a
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author Miller, Austin S.
Alexanian, Erik J.
author_facet Miller, Austin S.
Alexanian, Erik J.
author_sort Miller, Austin S.
collection PubMed
description 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.
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spelling pubmed-95804772022-10-31 Heteroarylation of unactivated C–H bonds suitable for late-stage functionalization Miller, Austin S. Alexanian, Erik J. Chem Sci Chemistry 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. The Royal Society of Chemistry 2022-09-26 /pmc/articles/PMC9580477/ /pubmed/36320922 http://dx.doi.org/10.1039/d2sc04605a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Miller, Austin S.
Alexanian, Erik J.
Heteroarylation of unactivated C–H bonds suitable for late-stage functionalization
title Heteroarylation of unactivated C–H bonds suitable for late-stage functionalization
title_full Heteroarylation of unactivated C–H bonds suitable for late-stage functionalization
title_fullStr Heteroarylation of unactivated C–H bonds suitable for late-stage functionalization
title_full_unstemmed Heteroarylation of unactivated C–H bonds suitable for late-stage functionalization
title_short Heteroarylation of unactivated C–H bonds suitable for late-stage functionalization
title_sort heteroarylation of unactivated c–h bonds suitable for late-stage functionalization
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9580477/
https://www.ncbi.nlm.nih.gov/pubmed/36320922
http://dx.doi.org/10.1039/d2sc04605a
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