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Homocouplings of Sodium Arenesulfinates: Selective Access to Symmetric Diaryl Sulfides and Diaryl Disulfides

Symmetrical diaryl sulfides and diaryl disulfides have been efficiently and selectively constructed via the homocoupling of sodium arenesulfinates. The selectivity of products relied on the different reaction systems: symmetrical diaryl sulfides were predominately obtained under the Pd(OAc)(2) catal...

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Autores principales: Yu, Xin-Zhang, Wei, Wen-Long, Niu, Yu-Lan, Li, Xing, Wang, Ming, Gao, Wen-Chao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9571168/
https://www.ncbi.nlm.nih.gov/pubmed/36234770
http://dx.doi.org/10.3390/molecules27196232
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author Yu, Xin-Zhang
Wei, Wen-Long
Niu, Yu-Lan
Li, Xing
Wang, Ming
Gao, Wen-Chao
author_facet Yu, Xin-Zhang
Wei, Wen-Long
Niu, Yu-Lan
Li, Xing
Wang, Ming
Gao, Wen-Chao
author_sort Yu, Xin-Zhang
collection PubMed
description Symmetrical diaryl sulfides and diaryl disulfides have been efficiently and selectively constructed via the homocoupling of sodium arenesulfinates. The selectivity of products relied on the different reaction systems: symmetrical diaryl sulfides were predominately obtained under the Pd(OAc)(2) catalysis, whereas symmetrical diaryl sulfides were exclusively yielded in the presence of the reductive Fe/HCl system.
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spelling pubmed-95711682022-10-17 Homocouplings of Sodium Arenesulfinates: Selective Access to Symmetric Diaryl Sulfides and Diaryl Disulfides Yu, Xin-Zhang Wei, Wen-Long Niu, Yu-Lan Li, Xing Wang, Ming Gao, Wen-Chao Molecules Article Symmetrical diaryl sulfides and diaryl disulfides have been efficiently and selectively constructed via the homocoupling of sodium arenesulfinates. The selectivity of products relied on the different reaction systems: symmetrical diaryl sulfides were predominately obtained under the Pd(OAc)(2) catalysis, whereas symmetrical diaryl sulfides were exclusively yielded in the presence of the reductive Fe/HCl system. MDPI 2022-09-22 /pmc/articles/PMC9571168/ /pubmed/36234770 http://dx.doi.org/10.3390/molecules27196232 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Yu, Xin-Zhang
Wei, Wen-Long
Niu, Yu-Lan
Li, Xing
Wang, Ming
Gao, Wen-Chao
Homocouplings of Sodium Arenesulfinates: Selective Access to Symmetric Diaryl Sulfides and Diaryl Disulfides
title Homocouplings of Sodium Arenesulfinates: Selective Access to Symmetric Diaryl Sulfides and Diaryl Disulfides
title_full Homocouplings of Sodium Arenesulfinates: Selective Access to Symmetric Diaryl Sulfides and Diaryl Disulfides
title_fullStr Homocouplings of Sodium Arenesulfinates: Selective Access to Symmetric Diaryl Sulfides and Diaryl Disulfides
title_full_unstemmed Homocouplings of Sodium Arenesulfinates: Selective Access to Symmetric Diaryl Sulfides and Diaryl Disulfides
title_short Homocouplings of Sodium Arenesulfinates: Selective Access to Symmetric Diaryl Sulfides and Diaryl Disulfides
title_sort homocouplings of sodium arenesulfinates: selective access to symmetric diaryl sulfides and diaryl disulfides
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9571168/
https://www.ncbi.nlm.nih.gov/pubmed/36234770
http://dx.doi.org/10.3390/molecules27196232
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