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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...

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Autores principales: Ángel, Alix Y. Bastidas, Campos, Philipe Raphael O., Alberto, Eduardo E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
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.
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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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