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Selenonium Salt as a Catalyst for Nucleophilic Substitution Reactions in Water: Synthesis of Thiocyanites and Selenocyanates
Organothiocyanates and selenocyanates are valuable compounds, both in terms of functional group interconversion and due to their biological activities. In this contribution, we report the synthesis of a series of these important substances in a mixture of water and dimethyl carbonate (20/1 proportio...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10095699/ https://www.ncbi.nlm.nih.gov/pubmed/37049818 http://dx.doi.org/10.3390/molecules28073056 |
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author | Ángel, Alix Y. Bastidas Campos, Philipe Raphael O. Alberto, Eduardo E. |
author_facet | Ángel, Alix Y. Bastidas Campos, Philipe Raphael O. Alberto, Eduardo E. |
author_sort | Ángel, Alix Y. Bastidas |
collection | PubMed |
description | Organothiocyanates and selenocyanates are valuable compounds, both in terms of functional group interconversion and due to their biological activities. In this contribution, we report the synthesis of a series of these important substances in a mixture of water and dimethyl carbonate (20/1 proportion) using potassium thio- or selenocyanates salts and organic bromides. The key to the effectiveness of the reaction is a chalcogen bond interaction between a selenonium salt catalyst and the organic substrate. |
format | Online Article Text |
id | pubmed-10095699 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-100956992023-04-13 Selenonium Salt as a Catalyst for Nucleophilic Substitution Reactions in Water: Synthesis of Thiocyanites and Selenocyanates Ángel, Alix Y. Bastidas Campos, Philipe Raphael O. Alberto, Eduardo E. Molecules Article Organothiocyanates and selenocyanates are valuable compounds, both in terms of functional group interconversion and due to their biological activities. In this contribution, we report the synthesis of a series of these important substances in a mixture of water and dimethyl carbonate (20/1 proportion) using potassium thio- or selenocyanates salts and organic bromides. The key to the effectiveness of the reaction is a chalcogen bond interaction between a selenonium salt catalyst and the organic substrate. MDPI 2023-03-29 /pmc/articles/PMC10095699/ /pubmed/37049818 http://dx.doi.org/10.3390/molecules28073056 Text en © 2023 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 Ángel, Alix Y. Bastidas Campos, Philipe Raphael O. Alberto, Eduardo E. Selenonium Salt as a Catalyst for Nucleophilic Substitution Reactions in Water: Synthesis of Thiocyanites and Selenocyanates |
title | Selenonium Salt as a Catalyst for Nucleophilic Substitution Reactions in Water: Synthesis of Thiocyanites and Selenocyanates |
title_full | Selenonium Salt as a Catalyst for Nucleophilic Substitution Reactions in Water: Synthesis of Thiocyanites and Selenocyanates |
title_fullStr | Selenonium Salt as a Catalyst for Nucleophilic Substitution Reactions in Water: Synthesis of Thiocyanites and Selenocyanates |
title_full_unstemmed | Selenonium Salt as a Catalyst for Nucleophilic Substitution Reactions in Water: Synthesis of Thiocyanites and Selenocyanates |
title_short | Selenonium Salt as a Catalyst for Nucleophilic Substitution Reactions in Water: Synthesis of Thiocyanites and Selenocyanates |
title_sort | selenonium salt as a catalyst for nucleophilic substitution reactions in water: synthesis of thiocyanites and selenocyanates |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10095699/ https://www.ncbi.nlm.nih.gov/pubmed/37049818 http://dx.doi.org/10.3390/molecules28073056 |
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