Strategies for the Synthesis of Fluorinated Nucleosides, Nucleotides and Oligonucleotides.
Fluorinating reagents
Nucleic acids
Nucleosides
Nucleotides
Site-selective Fluorination
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:
Sep 2022
Sep 2022
Historique:
revised:
11
05
2022
received:
25
03
2022
pubmed:
1
6
2022
medline:
14
9
2022
entrez:
31
5
2022
Statut:
ppublish
Résumé
Fluorinated nucleosides and oligonucleotides are of specific interest as probes for studying nucleic acids interaction, structures, biological transformations, and its biomedical applications. Among various modifications of oligonucleotides, fluorination of preformed nucleoside and/or nucleotides have recently gained attention owing to the unique properties of fluorine atoms imparting medicinal properties with respect to the small size, electronegativity, lipophilicity, and ability for stereochemical control. This review deals with synthetic protocols for selective fluorination either at sugar or base moiety in a preformed nucleosides, nucleotides and nucleic acids using specific fluorinating reagents.
Identifiants
pubmed: 35638251
doi: 10.1002/tcr.202200066
doi:
Substances chimiques
Nucleic Acids
0
Nucleosides
0
Nucleotides
0
Oligonucleotides
0
Fluorine
284SYP0193
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
e202200066Subventions
Organisme : CSIR
Informations de copyright
© 2022 The Chemical Society of Japan & Wiley-VCH GmbH.
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