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An Orthogonal Synthetic Approach to Nonsymmetrical Bisazolyl 2,4,6-Trisubstituted Pyridines
A three-step synthetic route giving access to nonsymmetrical bisazolyl 2,4,6-trisubstituted pyridines with different substituents on the pyrazole, indazole, and pyridine heterocycles is described. From the readily available 4-bromo-2,6-difluoropyridine, both fluorine atoms allow for easy selective s...
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/PMC8911976/ https://www.ncbi.nlm.nih.gov/pubmed/35268847 http://dx.doi.org/10.3390/molecules27051746 |
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author | Gamonal Ruiz-Crespo, Arturo Galán-Fernández, Laura Martínez-Martín, Paloma Rodríguez-Ubis, Juan Carlos |
author_facet | Gamonal Ruiz-Crespo, Arturo Galán-Fernández, Laura Martínez-Martín, Paloma Rodríguez-Ubis, Juan Carlos |
author_sort | Gamonal Ruiz-Crespo, Arturo |
collection | PubMed |
description | A three-step synthetic route giving access to nonsymmetrical bisazolyl 2,4,6-trisubstituted pyridines with different substituents on the pyrazole, indazole, and pyridine heterocycles is described. From the readily available 4-bromo-2,6-difluoropyridine, both fluorine atoms allow for easy selective stepwise substitution, and the bromine atom provides easy access to additional functionalities through both Suzuki and Sonogashira Pd(0) cross-coupling reactions. These synthons represent optimal structures as building blocks in complexation and metalloorganic structures for the tuning of their chelating and photophysical properties. |
format | Online Article Text |
id | pubmed-8911976 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-89119762022-03-11 An Orthogonal Synthetic Approach to Nonsymmetrical Bisazolyl 2,4,6-Trisubstituted Pyridines Gamonal Ruiz-Crespo, Arturo Galán-Fernández, Laura Martínez-Martín, Paloma Rodríguez-Ubis, Juan Carlos Molecules Article A three-step synthetic route giving access to nonsymmetrical bisazolyl 2,4,6-trisubstituted pyridines with different substituents on the pyrazole, indazole, and pyridine heterocycles is described. From the readily available 4-bromo-2,6-difluoropyridine, both fluorine atoms allow for easy selective stepwise substitution, and the bromine atom provides easy access to additional functionalities through both Suzuki and Sonogashira Pd(0) cross-coupling reactions. These synthons represent optimal structures as building blocks in complexation and metalloorganic structures for the tuning of their chelating and photophysical properties. MDPI 2022-03-07 /pmc/articles/PMC8911976/ /pubmed/35268847 http://dx.doi.org/10.3390/molecules27051746 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 Gamonal Ruiz-Crespo, Arturo Galán-Fernández, Laura Martínez-Martín, Paloma Rodríguez-Ubis, Juan Carlos An Orthogonal Synthetic Approach to Nonsymmetrical Bisazolyl 2,4,6-Trisubstituted Pyridines |
title | An Orthogonal Synthetic Approach to Nonsymmetrical Bisazolyl 2,4,6-Trisubstituted Pyridines |
title_full | An Orthogonal Synthetic Approach to Nonsymmetrical Bisazolyl 2,4,6-Trisubstituted Pyridines |
title_fullStr | An Orthogonal Synthetic Approach to Nonsymmetrical Bisazolyl 2,4,6-Trisubstituted Pyridines |
title_full_unstemmed | An Orthogonal Synthetic Approach to Nonsymmetrical Bisazolyl 2,4,6-Trisubstituted Pyridines |
title_short | An Orthogonal Synthetic Approach to Nonsymmetrical Bisazolyl 2,4,6-Trisubstituted Pyridines |
title_sort | orthogonal synthetic approach to nonsymmetrical bisazolyl 2,4,6-trisubstituted pyridines |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8911976/ https://www.ncbi.nlm.nih.gov/pubmed/35268847 http://dx.doi.org/10.3390/molecules27051746 |
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