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Direct halosulfonylation of alkynes: an overview

The difunctionalization reactions of easily available and inexpensive alkynes have emerged as a reliable, powerful, and step-economical approach for the construction of highly substituted complex alkenes in a one-pot manner, without the need for isolation of intermediates. A wide variety of transfor...

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Detalles Bibliográficos
Autores principales: Zhang, Yujun, Vessally, Esmail
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9042254/
https://www.ncbi.nlm.nih.gov/pubmed/35497552
http://dx.doi.org/10.1039/d1ra03443j
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author Zhang, Yujun
Vessally, Esmail
author_facet Zhang, Yujun
Vessally, Esmail
author_sort Zhang, Yujun
collection PubMed
description The difunctionalization reactions of easily available and inexpensive alkynes have emerged as a reliable, powerful, and step-economical approach for the construction of highly substituted complex alkenes in a one-pot manner, without the need for isolation of intermediates. A wide variety of transformations based on this concept have been successfully achieved for the preparation of synthetically and biologically important β-halovinyl sulfone scaffolds. In this Review, we summarize the recent advances and developments in this field and present a comprehensive overview of halosulfonylation of alkyne substrates with emphasis on the mechanistic features of the reactions.
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spelling pubmed-90422542022-04-28 Direct halosulfonylation of alkynes: an overview Zhang, Yujun Vessally, Esmail RSC Adv Chemistry The difunctionalization reactions of easily available and inexpensive alkynes have emerged as a reliable, powerful, and step-economical approach for the construction of highly substituted complex alkenes in a one-pot manner, without the need for isolation of intermediates. A wide variety of transformations based on this concept have been successfully achieved for the preparation of synthetically and biologically important β-halovinyl sulfone scaffolds. In this Review, we summarize the recent advances and developments in this field and present a comprehensive overview of halosulfonylation of alkyne substrates with emphasis on the mechanistic features of the reactions. The Royal Society of Chemistry 2021-10-13 /pmc/articles/PMC9042254/ /pubmed/35497552 http://dx.doi.org/10.1039/d1ra03443j Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Zhang, Yujun
Vessally, Esmail
Direct halosulfonylation of alkynes: an overview
title Direct halosulfonylation of alkynes: an overview
title_full Direct halosulfonylation of alkynes: an overview
title_fullStr Direct halosulfonylation of alkynes: an overview
title_full_unstemmed Direct halosulfonylation of alkynes: an overview
title_short Direct halosulfonylation of alkynes: an overview
title_sort direct halosulfonylation of alkynes: an overview
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9042254/
https://www.ncbi.nlm.nih.gov/pubmed/35497552
http://dx.doi.org/10.1039/d1ra03443j
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