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Multicomponent reactions in nucleoside chemistry
This review covers sixty original publications dealing with the application of multicomponent reactions (MCRs) in the synthesis of novel nucleoside analogs. The reported approaches were employed for modifications of the parent nucleoside core or for de novo construction of a nucleoside scaffold from...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4142899/ https://www.ncbi.nlm.nih.gov/pubmed/25161730 http://dx.doi.org/10.3762/bjoc.10.179 |
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author | Koszytkowska-Stawińska, Mariola Buchowicz, Włodzimierz |
author_facet | Koszytkowska-Stawińska, Mariola Buchowicz, Włodzimierz |
author_sort | Koszytkowska-Stawińska, Mariola |
collection | PubMed |
description | This review covers sixty original publications dealing with the application of multicomponent reactions (MCRs) in the synthesis of novel nucleoside analogs. The reported approaches were employed for modifications of the parent nucleoside core or for de novo construction of a nucleoside scaffold from non-nucleoside substrates. The cited references are grouped according to the usually recognized types of the MCRs. Biochemical properties of the novel nucleoside analogs are also presented (if provided by the authors). |
format | Online Article Text |
id | pubmed-4142899 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-41428992014-08-26 Multicomponent reactions in nucleoside chemistry Koszytkowska-Stawińska, Mariola Buchowicz, Włodzimierz Beilstein J Org Chem Review This review covers sixty original publications dealing with the application of multicomponent reactions (MCRs) in the synthesis of novel nucleoside analogs. The reported approaches were employed for modifications of the parent nucleoside core or for de novo construction of a nucleoside scaffold from non-nucleoside substrates. The cited references are grouped according to the usually recognized types of the MCRs. Biochemical properties of the novel nucleoside analogs are also presented (if provided by the authors). Beilstein-Institut 2014-07-29 /pmc/articles/PMC4142899/ /pubmed/25161730 http://dx.doi.org/10.3762/bjoc.10.179 Text en Copyright © 2014, Koszytkowska-Stawińska and Buchowicz https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms) |
spellingShingle | Review Koszytkowska-Stawińska, Mariola Buchowicz, Włodzimierz Multicomponent reactions in nucleoside chemistry |
title | Multicomponent reactions in nucleoside chemistry |
title_full | Multicomponent reactions in nucleoside chemistry |
title_fullStr | Multicomponent reactions in nucleoside chemistry |
title_full_unstemmed | Multicomponent reactions in nucleoside chemistry |
title_short | Multicomponent reactions in nucleoside chemistry |
title_sort | multicomponent reactions in nucleoside chemistry |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4142899/ https://www.ncbi.nlm.nih.gov/pubmed/25161730 http://dx.doi.org/10.3762/bjoc.10.179 |
work_keys_str_mv | AT koszytkowskastawinskamariola multicomponentreactionsinnucleosidechemistry AT buchowiczwłodzimierz multicomponentreactionsinnucleosidechemistry |