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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...

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Autores principales: Begini, Francesca, Balaguez, Renata A., Larroza, Allya, Lopes, Eric F., Lenardão, Eder João, Santi, Claudio, Alves, Diego
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
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.
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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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