Protecting-group-free synthesis of clevudine (l-FMAU), a treatment of the hepatitis B virus
Author:
Affiliation:
1. Département de Chimie, 1045 av. De la Médecine, Université Laval, Québec City, Qc, Canada G1V 0A6
Abstract
Funder
Université Laval
Fonds de recherche du Québec – Nature et technologies
Natural Sciences and Engineering Research Council of Canada
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2022/OB/D2OB01814D
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1. The evolution of nucleoside analogue antivirals: A review for chemists and non-chemists. Part 1: Early structural modifications to the nucleoside scaffold
2. The evolution of antiviral nucleoside analogues: A review for chemists and non-chemists. Part II: Complex modifications to the nucleoside scaffold
3. Nucleoside Analogues as Antibacterial Agents
4. Discovery and Synthesis of a Phosphoramidate Prodrug of a Pyrrolo[2,1-f][triazin-4-amino] Adenine C-Nucleoside (GS-5734) for the Treatment of Ebola and Emerging Viruses
5. RNA-dependent RNA polymerase (RdRp) inhibitors: The current landscape and repurposing for the COVID-19 pandemic
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