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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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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. |
format | Online Article Text |
id | pubmed-9571168 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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