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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...

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Autores principales: Jahnz-Wechmann, Zofia, Framski, Grzegorz R., Januszczyk, Piotr A., Boryski, Jerzy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
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.
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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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