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One-pot thiol-free synthetic approach to sulfides, and sulfoxides selectively

A facile and efficient thiol-free one-pot method for direct synthesis of sulfides and sulfoxides under green conditions without using any metal catalyst is reported. For this purpose, we used benzyl bromides as starting materials in the presence of potassium thioacetate (PTA) and Oxone® which are lo...

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Detalles Bibliográficos
Autores principales: Kotha, Sambasivarao, Gupta, Naveen Kumar, Ansari, Saima
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9443682/
https://www.ncbi.nlm.nih.gov/pubmed/36199306
http://dx.doi.org/10.1039/d2ra04872h
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author Kotha, Sambasivarao
Gupta, Naveen Kumar
Ansari, Saima
author_facet Kotha, Sambasivarao
Gupta, Naveen Kumar
Ansari, Saima
author_sort Kotha, Sambasivarao
collection PubMed
description A facile and efficient thiol-free one-pot method for direct synthesis of sulfides and sulfoxides under green conditions without using any metal catalyst is reported. For this purpose, we used benzyl bromides as starting materials in the presence of potassium thioacetate (PTA) and Oxone® which are low-cost, and readily accessible chemicals. This method is highly compatible with a variety of functional groups and delivered a series of sulfides, bis-sulfides, and sulfoxides in good yields. The selective formation of sulfoxides over sulfones is discussed via a mechanism.
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spelling pubmed-94436822022-10-04 One-pot thiol-free synthetic approach to sulfides, and sulfoxides selectively Kotha, Sambasivarao Gupta, Naveen Kumar Ansari, Saima RSC Adv Chemistry A facile and efficient thiol-free one-pot method for direct synthesis of sulfides and sulfoxides under green conditions without using any metal catalyst is reported. For this purpose, we used benzyl bromides as starting materials in the presence of potassium thioacetate (PTA) and Oxone® which are low-cost, and readily accessible chemicals. This method is highly compatible with a variety of functional groups and delivered a series of sulfides, bis-sulfides, and sulfoxides in good yields. The selective formation of sulfoxides over sulfones is discussed via a mechanism. The Royal Society of Chemistry 2022-09-05 /pmc/articles/PMC9443682/ /pubmed/36199306 http://dx.doi.org/10.1039/d2ra04872h Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Kotha, Sambasivarao
Gupta, Naveen Kumar
Ansari, Saima
One-pot thiol-free synthetic approach to sulfides, and sulfoxides selectively
title One-pot thiol-free synthetic approach to sulfides, and sulfoxides selectively
title_full One-pot thiol-free synthetic approach to sulfides, and sulfoxides selectively
title_fullStr One-pot thiol-free synthetic approach to sulfides, and sulfoxides selectively
title_full_unstemmed One-pot thiol-free synthetic approach to sulfides, and sulfoxides selectively
title_short One-pot thiol-free synthetic approach to sulfides, and sulfoxides selectively
title_sort one-pot thiol-free synthetic approach to sulfides, and sulfoxides selectively
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9443682/
https://www.ncbi.nlm.nih.gov/pubmed/36199306
http://dx.doi.org/10.1039/d2ra04872h
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