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Synthesis of 4-Arylselanyl-1H-1,2,3-triazoles from Selenium-Containing Carbinols
In this work, we present a simple way to achieve 4-arylselanyl-1H-1,2,3-triazoles from selenium-containing carbinols in a one-pot strategy. The selenium-containing carbinols were used as starting materials to produce a range of selanyl-triazoles in moderate to good yields, including a quinoline and...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8070154/ https://www.ncbi.nlm.nih.gov/pubmed/33921473 http://dx.doi.org/10.3390/molecules26082224 |
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author | Begini, Francesca Balaguez, Renata A. Larroza, Allya Lopes, Eric F. Lenardão, Eder João Santi, Claudio Alves, Diego |
author_facet | Begini, Francesca Balaguez, Renata A. Larroza, Allya Lopes, Eric F. Lenardão, Eder João Santi, Claudio Alves, Diego |
author_sort | Begini, Francesca |
collection | PubMed |
description | In this work, we present a simple way to achieve 4-arylselanyl-1H-1,2,3-triazoles from selenium-containing carbinols in a one-pot strategy. The selenium-containing carbinols were used as starting materials to produce a range of selanyl-triazoles in moderate to good yields, including a quinoline and Zidovudine derivatives. One-pot protocols are crucial to the current concerns about waste production and solvent consumption, avoiding the isolation and purification steps of the reactive terminal selanylalkynes. We could also isolate an interesting and unprecedented by-product with one alkynylselenium moiety connected to the triazole. |
format | Online Article Text |
id | pubmed-8070154 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-80701542021-04-26 Synthesis of 4-Arylselanyl-1H-1,2,3-triazoles from Selenium-Containing Carbinols Begini, Francesca Balaguez, Renata A. Larroza, Allya Lopes, Eric F. Lenardão, Eder João Santi, Claudio Alves, Diego Molecules Article In this work, we present a simple way to achieve 4-arylselanyl-1H-1,2,3-triazoles from selenium-containing carbinols in a one-pot strategy. The selenium-containing carbinols were used as starting materials to produce a range of selanyl-triazoles in moderate to good yields, including a quinoline and Zidovudine derivatives. One-pot protocols are crucial to the current concerns about waste production and solvent consumption, avoiding the isolation and purification steps of the reactive terminal selanylalkynes. We could also isolate an interesting and unprecedented by-product with one alkynylselenium moiety connected to the triazole. MDPI 2021-04-12 /pmc/articles/PMC8070154/ /pubmed/33921473 http://dx.doi.org/10.3390/molecules26082224 Text en © 2021 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 Begini, Francesca Balaguez, Renata A. Larroza, Allya Lopes, Eric F. Lenardão, Eder João Santi, Claudio Alves, Diego Synthesis of 4-Arylselanyl-1H-1,2,3-triazoles from Selenium-Containing Carbinols |
title | Synthesis of 4-Arylselanyl-1H-1,2,3-triazoles from Selenium-Containing Carbinols |
title_full | Synthesis of 4-Arylselanyl-1H-1,2,3-triazoles from Selenium-Containing Carbinols |
title_fullStr | Synthesis of 4-Arylselanyl-1H-1,2,3-triazoles from Selenium-Containing Carbinols |
title_full_unstemmed | Synthesis of 4-Arylselanyl-1H-1,2,3-triazoles from Selenium-Containing Carbinols |
title_short | Synthesis of 4-Arylselanyl-1H-1,2,3-triazoles from Selenium-Containing Carbinols |
title_sort | synthesis of 4-arylselanyl-1h-1,2,3-triazoles from selenium-containing carbinols |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8070154/ https://www.ncbi.nlm.nih.gov/pubmed/33921473 http://dx.doi.org/10.3390/molecules26082224 |
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