2- and 3-Fluoro-3-deaza-1′,6′-isoneplanocin: Synthesis and antiviral properties (including Ebola and Marburg)
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry
Reference15 articles.
1. Seley-Radtke, K.L.; Yates, K.L. The evolution of nucleoside analogue antivirals: A review for chemists and non-chemists. Part 1: Early structural modifications to the nucleoside scaffold. Antiviral Res. 2018, 154, 66-86. j.antiviral.2018.04.004.
2. Ye, W.; Schneller, S.W. The enantiomers of the 1',6'-isomer of neplanocin A: Synthesis and antiviral properties. Bioorg. Med. Chem. 2014, 22, 5315-5319. j.bmcl.2019.07.021.
3. Liu, C.; Chen, Q.; Schneller, S.W. Enantiomeric 3-deaza-1',6'-isoneplanocin and its 3-bromo analogue: Synthesis by the Ullmann reaction and their antiviral properties Bioorg. Med. Chem. Lett. 2016, 26, 928-930. j.bmcl.2015.12.061.
4. Liu, C.; Coleman, R.; Archer, A.; Hussein, I.; Bowlin, T.; Chen, Q.; Schneller, S.W. Enantiomeric 4'-truncated 3-deaza-1',6'-isoneplanocins: Synthesis and antiviral properties including Ebola. Bioorg. Med. Chem. Lett. 2019, 29, 2480-2482. j.bmcl.2019.07.021.
5. Synthesis of D-Like and L-like 5’fluoro-5’-deoxy-1’,6’-isoneplanocins and their antiviral activity;Liu;Nucleosides Nucleic Acids,2020
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