Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Mukhin, E. M., Savateev, K. V., Rusinov, V. L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2023
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
_version_ 1785023461622546432
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