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Approaches to the synthesis of heterocyclic C-nucleosides
This review is focused on the synthetic strategies to heterocyclic C-nucleosides and covers the literature from 2011 to 2021. The main attention is paid to the following three approaches: the direct C—C coupling of a carbohydrate moiety with a preformed aglycon unit, the construction of a (pseudo)su...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10092924/ https://www.ncbi.nlm.nih.gov/pubmed/37073401 http://dx.doi.org/10.1007/s11172-023-3810-1 |
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author | Mukhin, E. M. Savateev, K. V. Rusinov, V. L. |
author_facet | Mukhin, E. M. Savateev, K. V. Rusinov, V. L. |
author_sort | Mukhin, E. M. |
collection | PubMed |
description | This review is focused on the synthetic strategies to heterocyclic C-nucleosides and covers the literature from 2011 to 2021. The main attention is paid to the following three approaches: the direct C—C coupling of a carbohydrate moiety with a preformed aglycon unit, the construction of a (pseudo)sugar residue on a pre-formed aglycon, and the construction of an aglycon on a pre-formed (pseudo)sugar. In each Section, the literature data are categorized in terms of the size of aglycon from simple to complex, the advantages and drawbacks of the reviewed approaches are discussed. |
format | Online Article Text |
id | pubmed-10092924 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-100929242023-04-14 Approaches to the synthesis of heterocyclic C-nucleosides Mukhin, E. M. Savateev, K. V. Rusinov, V. L. Russ Chem Bull Review This review is focused on the synthetic strategies to heterocyclic C-nucleosides and covers the literature from 2011 to 2021. The main attention is paid to the following three approaches: the direct C—C coupling of a carbohydrate moiety with a preformed aglycon unit, the construction of a (pseudo)sugar residue on a pre-formed aglycon, and the construction of an aglycon on a pre-formed (pseudo)sugar. In each Section, the literature data are categorized in terms of the size of aglycon from simple to complex, the advantages and drawbacks of the reviewed approaches are discussed. Springer US 2023-04-12 2023 /pmc/articles/PMC10092924/ /pubmed/37073401 http://dx.doi.org/10.1007/s11172-023-3810-1 Text en © Springer Science+Business Media LLC 2023 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Review Mukhin, E. M. Savateev, K. V. Rusinov, V. L. Approaches to the synthesis of heterocyclic C-nucleosides |
title | Approaches to the synthesis of heterocyclic C-nucleosides |
title_full | Approaches to the synthesis of heterocyclic C-nucleosides |
title_fullStr | Approaches to the synthesis of heterocyclic C-nucleosides |
title_full_unstemmed | Approaches to the synthesis of heterocyclic C-nucleosides |
title_short | Approaches to the synthesis of heterocyclic C-nucleosides |
title_sort | approaches to the synthesis of heterocyclic c-nucleosides |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10092924/ https://www.ncbi.nlm.nih.gov/pubmed/37073401 http://dx.doi.org/10.1007/s11172-023-3810-1 |
work_keys_str_mv | AT mukhinem approachestothesynthesisofheterocycliccnucleosides AT savateevkv approachestothesynthesisofheterocycliccnucleosides AT rusinovvl approachestothesynthesisofheterocycliccnucleosides |