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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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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. |
format | Online Article Text |
id | pubmed-9042254 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT zhangyujun directhalosulfonylationofalkynesanoverview AT vessallyesmail directhalosulfonylationofalkynesanoverview |