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Alkoxysulfenylation of alkenes: development and recent advances
Among the wide variety of synthetic transformations of inexpensive and abundant feedstock alkenes, vicinal difunctionalization of carbon–carbon double bonds represent one of the most powerful and effective strategies for the introduction of two distinct functional groups into target compounds in a o...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9041976/ https://www.ncbi.nlm.nih.gov/pubmed/35495514 http://dx.doi.org/10.1039/d1ra03980f |
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author | Cao, Yan Soleimani-Amiri, Somayeh Ahmadi, Roya Issakhov, Alibek Ebadi, Abdol Ghaffar Vessally, Esmail |
author_facet | Cao, Yan Soleimani-Amiri, Somayeh Ahmadi, Roya Issakhov, Alibek Ebadi, Abdol Ghaffar Vessally, Esmail |
author_sort | Cao, Yan |
collection | PubMed |
description | Among the wide variety of synthetic transformations of inexpensive and abundant feedstock alkenes, vicinal difunctionalization of carbon–carbon double bonds represent one of the most powerful and effective strategies for the introduction of two distinct functional groups into target compounds in a one-pot process. In this context, the direct alkoxysulfenylation of alkenes has emerged as an elegant method to construct valuable β-alkoxy sulfides in an atom- and pot-economic manner utilizing readily accessible starting materials. Here, we review the available literature on this appealing research topic by hoping that it will be beneficial for eliciting further research and thinking in this domain. |
format | Online Article Text |
id | pubmed-9041976 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90419762022-04-28 Alkoxysulfenylation of alkenes: development and recent advances Cao, Yan Soleimani-Amiri, Somayeh Ahmadi, Roya Issakhov, Alibek Ebadi, Abdol Ghaffar Vessally, Esmail RSC Adv Chemistry Among the wide variety of synthetic transformations of inexpensive and abundant feedstock alkenes, vicinal difunctionalization of carbon–carbon double bonds represent one of the most powerful and effective strategies for the introduction of two distinct functional groups into target compounds in a one-pot process. In this context, the direct alkoxysulfenylation of alkenes has emerged as an elegant method to construct valuable β-alkoxy sulfides in an atom- and pot-economic manner utilizing readily accessible starting materials. Here, we review the available literature on this appealing research topic by hoping that it will be beneficial for eliciting further research and thinking in this domain. The Royal Society of Chemistry 2021-10-01 /pmc/articles/PMC9041976/ /pubmed/35495514 http://dx.doi.org/10.1039/d1ra03980f Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Cao, Yan Soleimani-Amiri, Somayeh Ahmadi, Roya Issakhov, Alibek Ebadi, Abdol Ghaffar Vessally, Esmail Alkoxysulfenylation of alkenes: development and recent advances |
title | Alkoxysulfenylation of alkenes: development and recent advances |
title_full | Alkoxysulfenylation of alkenes: development and recent advances |
title_fullStr | Alkoxysulfenylation of alkenes: development and recent advances |
title_full_unstemmed | Alkoxysulfenylation of alkenes: development and recent advances |
title_short | Alkoxysulfenylation of alkenes: development and recent advances |
title_sort | alkoxysulfenylation of alkenes: development and recent advances |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9041976/ https://www.ncbi.nlm.nih.gov/pubmed/35495514 http://dx.doi.org/10.1039/d1ra03980f |
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