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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...

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Autores principales: Cao, Yan, Soleimani-Amiri, Somayeh, Ahmadi, Roya, Issakhov, Alibek, Ebadi, Abdol Ghaffar, 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/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.
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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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