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Syntheses of Isoxazoline-Carbocyclic Nucleosides and Their Antiviral Evaluation: A Standard Protocol

The current synthesis of racemic purine and pyrimidine isoxazoline-carbocyclic nucleosides is reported, detailing the key-steps for standard and reliable preparations. Improved yields were obtained by the proper tuning of the single synthetic steps, opening the way for the preparation of a variety o...

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Detalles Bibliográficos
Autores principales: Quadrelli, Paolo, Vazquez Martinez, Naiara, Scrocchi, Roberto, Corsaro, Antonino, Pistarà, Venerando
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4230217/
https://www.ncbi.nlm.nih.gov/pubmed/25544956
http://dx.doi.org/10.1155/2014/492178
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author Quadrelli, Paolo
Vazquez Martinez, Naiara
Scrocchi, Roberto
Corsaro, Antonino
Pistarà, Venerando
author_facet Quadrelli, Paolo
Vazquez Martinez, Naiara
Scrocchi, Roberto
Corsaro, Antonino
Pistarà, Venerando
author_sort Quadrelli, Paolo
collection PubMed
description The current synthesis of racemic purine and pyrimidine isoxazoline-carbocyclic nucleosides is reported, detailing the key-steps for standard and reliable preparations. Improved yields were obtained by the proper tuning of the single synthetic steps, opening the way for the preparation of a variety of novel compounds. Some of the obtained compounds were also evaluated against a wide variety of DNA and RNA viruses including HIV. No specific antiviral activity was observed in the cases at hand. Novel compounds were prepared for future biological tests.
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spelling pubmed-42302172014-12-28 Syntheses of Isoxazoline-Carbocyclic Nucleosides and Their Antiviral Evaluation: A Standard Protocol Quadrelli, Paolo Vazquez Martinez, Naiara Scrocchi, Roberto Corsaro, Antonino Pistarà, Venerando ScientificWorldJournal Research Article The current synthesis of racemic purine and pyrimidine isoxazoline-carbocyclic nucleosides is reported, detailing the key-steps for standard and reliable preparations. Improved yields were obtained by the proper tuning of the single synthetic steps, opening the way for the preparation of a variety of novel compounds. Some of the obtained compounds were also evaluated against a wide variety of DNA and RNA viruses including HIV. No specific antiviral activity was observed in the cases at hand. Novel compounds were prepared for future biological tests. Hindawi Publishing Corporation 2014 2014-10-30 /pmc/articles/PMC4230217/ /pubmed/25544956 http://dx.doi.org/10.1155/2014/492178 Text en Copyright © 2014 Paolo Quadrelli et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Quadrelli, Paolo
Vazquez Martinez, Naiara
Scrocchi, Roberto
Corsaro, Antonino
Pistarà, Venerando
Syntheses of Isoxazoline-Carbocyclic Nucleosides and Their Antiviral Evaluation: A Standard Protocol
title Syntheses of Isoxazoline-Carbocyclic Nucleosides and Their Antiviral Evaluation: A Standard Protocol
title_full Syntheses of Isoxazoline-Carbocyclic Nucleosides and Their Antiviral Evaluation: A Standard Protocol
title_fullStr Syntheses of Isoxazoline-Carbocyclic Nucleosides and Their Antiviral Evaluation: A Standard Protocol
title_full_unstemmed Syntheses of Isoxazoline-Carbocyclic Nucleosides and Their Antiviral Evaluation: A Standard Protocol
title_short Syntheses of Isoxazoline-Carbocyclic Nucleosides and Their Antiviral Evaluation: A Standard Protocol
title_sort syntheses of isoxazoline-carbocyclic nucleosides and their antiviral evaluation: a standard protocol
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4230217/
https://www.ncbi.nlm.nih.gov/pubmed/25544956
http://dx.doi.org/10.1155/2014/492178
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