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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
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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. |
format | Online Article Text |
id | pubmed-4230217 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
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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