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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2022
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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. |
format | Online Article Text |
id | pubmed-9443682 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
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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