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Continuous Bioinspired Oxidation of Sulfides
A simple, efficient, and selective oxidation under flow conditions of sulfides into their corresponding sulfoxides and sulfones is reported herein, using as a catalyst perselenic acid generated in situ by the oxidation of selenium (IV) oxide in a diluted aqueous solution of hydrogen peroxide as the...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7321102/ https://www.ncbi.nlm.nih.gov/pubmed/32545303 http://dx.doi.org/10.3390/molecules25112711 |
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author | Mangiavacchi, Francesca Crociani, Letizia Sancineto, Luca Marini, Francesca Santi, Claudio |
author_facet | Mangiavacchi, Francesca Crociani, Letizia Sancineto, Luca Marini, Francesca Santi, Claudio |
author_sort | Mangiavacchi, Francesca |
collection | PubMed |
description | A simple, efficient, and selective oxidation under flow conditions of sulfides into their corresponding sulfoxides and sulfones is reported herein, using as a catalyst perselenic acid generated in situ by the oxidation of selenium (IV) oxide in a diluted aqueous solution of hydrogen peroxide as the final oxidant. The scope of the proposed methodology was investigated using aryl alkyl sulfides, aryl vinyl sulfides, and dialkyl sulfides as substrates, evidencing, in general, a good applicability. The scaled-up synthesis of (methylsulfonyl)benzene was also demonstrated, leading to its gram-scale preparation. |
format | Online Article Text |
id | pubmed-7321102 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-73211022020-07-06 Continuous Bioinspired Oxidation of Sulfides Mangiavacchi, Francesca Crociani, Letizia Sancineto, Luca Marini, Francesca Santi, Claudio Molecules Communication A simple, efficient, and selective oxidation under flow conditions of sulfides into their corresponding sulfoxides and sulfones is reported herein, using as a catalyst perselenic acid generated in situ by the oxidation of selenium (IV) oxide in a diluted aqueous solution of hydrogen peroxide as the final oxidant. The scope of the proposed methodology was investigated using aryl alkyl sulfides, aryl vinyl sulfides, and dialkyl sulfides as substrates, evidencing, in general, a good applicability. The scaled-up synthesis of (methylsulfonyl)benzene was also demonstrated, leading to its gram-scale preparation. MDPI 2020-06-11 /pmc/articles/PMC7321102/ /pubmed/32545303 http://dx.doi.org/10.3390/molecules25112711 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Communication Mangiavacchi, Francesca Crociani, Letizia Sancineto, Luca Marini, Francesca Santi, Claudio Continuous Bioinspired Oxidation of Sulfides |
title | Continuous Bioinspired Oxidation of Sulfides |
title_full | Continuous Bioinspired Oxidation of Sulfides |
title_fullStr | Continuous Bioinspired Oxidation of Sulfides |
title_full_unstemmed | Continuous Bioinspired Oxidation of Sulfides |
title_short | Continuous Bioinspired Oxidation of Sulfides |
title_sort | continuous bioinspired oxidation of sulfides |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7321102/ https://www.ncbi.nlm.nih.gov/pubmed/32545303 http://dx.doi.org/10.3390/molecules25112711 |
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