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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2022
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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. |
format | Online Article Text |
id | pubmed-9580477 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
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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