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Base-Modified Nucleosides: Etheno Derivatives
This review presents synthesis and chemistry of nucleoside analogs, possessing an additional fused, heterocyclic ring of the “etheno” type, such as 1,N(6)-ethenoadenosine, 1,N(4)-ethenocytidine, 1,N(2)-ethenoguanosine, and other related derivatives. Formation of ethenonucleosides, in the presence of...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4848297/ https://www.ncbi.nlm.nih.gov/pubmed/27200341 http://dx.doi.org/10.3389/fchem.2016.00019 |
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author | Jahnz-Wechmann, Zofia Framski, Grzegorz R. Januszczyk, Piotr A. Boryski, Jerzy |
author_facet | Jahnz-Wechmann, Zofia Framski, Grzegorz R. Januszczyk, Piotr A. Boryski, Jerzy |
author_sort | Jahnz-Wechmann, Zofia |
collection | PubMed |
description | This review presents synthesis and chemistry of nucleoside analogs, possessing an additional fused, heterocyclic ring of the “etheno” type, such as 1,N(6)-ethenoadenosine, 1,N(4)-ethenocytidine, 1,N(2)-ethenoguanosine, and other related derivatives. Formation of ethenonucleosides, in the presence of α-halocarbonyl reagents and their mechanism, stability, and degradation, reactions of substitution and transglycosylation, as well as their application in the nucleoside synthesis, have been described. Some of the discussed compounds may be applied as chemotherapeutic agents in antiviral and anticancer treatment, acting as pro-nucleosides of already known, biologically active nucleoside analogs. |
format | Online Article Text |
id | pubmed-4848297 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-48482972016-05-19 Base-Modified Nucleosides: Etheno Derivatives Jahnz-Wechmann, Zofia Framski, Grzegorz R. Januszczyk, Piotr A. Boryski, Jerzy Front Chem Chemistry This review presents synthesis and chemistry of nucleoside analogs, possessing an additional fused, heterocyclic ring of the “etheno” type, such as 1,N(6)-ethenoadenosine, 1,N(4)-ethenocytidine, 1,N(2)-ethenoguanosine, and other related derivatives. Formation of ethenonucleosides, in the presence of α-halocarbonyl reagents and their mechanism, stability, and degradation, reactions of substitution and transglycosylation, as well as their application in the nucleoside synthesis, have been described. Some of the discussed compounds may be applied as chemotherapeutic agents in antiviral and anticancer treatment, acting as pro-nucleosides of already known, biologically active nucleoside analogs. Frontiers Media S.A. 2016-04-28 /pmc/articles/PMC4848297/ /pubmed/27200341 http://dx.doi.org/10.3389/fchem.2016.00019 Text en Copyright © 2016 Jahnz-Wechmann, Framski, Januszczyk and Boryski. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Chemistry Jahnz-Wechmann, Zofia Framski, Grzegorz R. Januszczyk, Piotr A. Boryski, Jerzy Base-Modified Nucleosides: Etheno Derivatives |
title | Base-Modified Nucleosides: Etheno Derivatives |
title_full | Base-Modified Nucleosides: Etheno Derivatives |
title_fullStr | Base-Modified Nucleosides: Etheno Derivatives |
title_full_unstemmed | Base-Modified Nucleosides: Etheno Derivatives |
title_short | Base-Modified Nucleosides: Etheno Derivatives |
title_sort | base-modified nucleosides: etheno derivatives |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4848297/ https://www.ncbi.nlm.nih.gov/pubmed/27200341 http://dx.doi.org/10.3389/fchem.2016.00019 |
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