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Transition-Metal-Free Highly Efficient Aerobic Oxidation of Sulfides to Sulfoxides under Mild Conditions

A highly efficient transition-metal-free catalytic system Br(2)/NaNO(2)/H(2)O has been developed for a robust and economic acid-free aerobic oxidation of sulfides. It is noteworthy that the sulfide function reacts under mild conditions without over-oxidation to sulfone. The role of NaNO(2) as an eff...

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Autores principales: Zhang, Hua, Chen, Chunyu, Liu, Renhua, Xu, Qiang, Zhao, Weiqie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257055/
https://www.ncbi.nlm.nih.gov/pubmed/20110873
http://dx.doi.org/10.3390/molecules15010083
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author Zhang, Hua
Chen, Chunyu
Liu, Renhua
Xu, Qiang
Zhao, Weiqie
author_facet Zhang, Hua
Chen, Chunyu
Liu, Renhua
Xu, Qiang
Zhao, Weiqie
author_sort Zhang, Hua
collection PubMed
description A highly efficient transition-metal-free catalytic system Br(2)/NaNO(2)/H(2)O has been developed for a robust and economic acid-free aerobic oxidation of sulfides. It is noteworthy that the sulfide function reacts under mild conditions without over-oxidation to sulfone. The role of NaNO(2) as an efficient NO equivalent for the activation of molecular oxygen was identified. Under the optimal conditions, a broad range of sulfide substrates were converted into their corresponding sulfoxides in high yields by molecular oxygen. The present catalytic system utilizes cheap and readily available agents as the catalysts, exhibits high selectivity for sulfoxide products and releases only innocuous water as the by-products.
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spelling pubmed-62570552018-12-03 Transition-Metal-Free Highly Efficient Aerobic Oxidation of Sulfides to Sulfoxides under Mild Conditions Zhang, Hua Chen, Chunyu Liu, Renhua Xu, Qiang Zhao, Weiqie Molecules Article A highly efficient transition-metal-free catalytic system Br(2)/NaNO(2)/H(2)O has been developed for a robust and economic acid-free aerobic oxidation of sulfides. It is noteworthy that the sulfide function reacts under mild conditions without over-oxidation to sulfone. The role of NaNO(2) as an efficient NO equivalent for the activation of molecular oxygen was identified. Under the optimal conditions, a broad range of sulfide substrates were converted into their corresponding sulfoxides in high yields by molecular oxygen. The present catalytic system utilizes cheap and readily available agents as the catalysts, exhibits high selectivity for sulfoxide products and releases only innocuous water as the by-products. Molecular Diversity Preservation International 2009-12-28 /pmc/articles/PMC6257055/ /pubmed/20110873 http://dx.doi.org/10.3390/molecules15010083 Text en © 2010 by the authors; http://creativecommons.org/licenses/by/3.0/ licensee Molecular Diversity Preservation International, Basel, Switzerland. This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Zhang, Hua
Chen, Chunyu
Liu, Renhua
Xu, Qiang
Zhao, Weiqie
Transition-Metal-Free Highly Efficient Aerobic Oxidation of Sulfides to Sulfoxides under Mild Conditions
title Transition-Metal-Free Highly Efficient Aerobic Oxidation of Sulfides to Sulfoxides under Mild Conditions
title_full Transition-Metal-Free Highly Efficient Aerobic Oxidation of Sulfides to Sulfoxides under Mild Conditions
title_fullStr Transition-Metal-Free Highly Efficient Aerobic Oxidation of Sulfides to Sulfoxides under Mild Conditions
title_full_unstemmed Transition-Metal-Free Highly Efficient Aerobic Oxidation of Sulfides to Sulfoxides under Mild Conditions
title_short Transition-Metal-Free Highly Efficient Aerobic Oxidation of Sulfides to Sulfoxides under Mild Conditions
title_sort transition-metal-free highly efficient aerobic oxidation of sulfides to sulfoxides under mild conditions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257055/
https://www.ncbi.nlm.nih.gov/pubmed/20110873
http://dx.doi.org/10.3390/molecules15010083
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