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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...

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Autores principales: Mangiavacchi, Francesca, Crociani, Letizia, Sancineto, Luca, Marini, Francesca, Santi, Claudio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
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.
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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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