Chemical Approaches to Carbocyclic Nucleosides.
antiviral compounds
carbocyclic nucleosides
transition-metal-catalyzed reactions
Journal
Chemical record (New York, N.Y.)
ISSN: 1528-0691
Titre abrégé: Chem Rec
Pays: United States
ID NLM: 101085550
Informations de publication
Date de publication:
May 2022
May 2022
Historique:
revised:
22
01
2022
received:
01
12
2021
pubmed:
5
2
2022
medline:
18
5
2022
entrez:
4
2
2022
Statut:
ppublish
Résumé
Nucleoside analogues are at the forefront of antiviral therapy for last decades. To circumvent some of their limitations, based on their metabolism, and in order to improve their anti-viral potency and selectivity, several families of nucleoside analogues have been described through structural modifications at the sugar and heterocycles. The replacement of the oxygen of the nucleoside by a methylene has led to the family of carbocyclic (or cyclopentane) nucleoside analogues. Various potent anti-HIV and anti-HBV drugs belong to this family. Main syntheses of carbocyclic analogues of nucleosides used Diels-Alder reactions (in racemic or asymmetric series), but also started from carbohydrates (ribose, glucose), as a source of optically active compounds, which then had to be transformed into carbacycles under various conditions. The growing interest in carbocyclic nucleosides has led several groups, including ours, to develop new analogues and to explore novel routes. This article will review some of the recent chemistry developed on selected five-membered ring carbocyclic nucleosides.
Identifiants
pubmed: 35119191
doi: 10.1002/tcr.202100307
doi:
Substances chimiques
Antiviral Agents
0
Nucleosides
0
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
e202100307Subventions
Organisme : Université d'Orléans
Organisme : French CNRS
Organisme : GAVO consortium
Organisme : FEDER FérI consortium
Informations de copyright
© 2022 The Chemical Society of Japan & Wiley-VCH GmbH.
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