Olefin Cross‐Metathesis for the Synthesis of Alkenyl Acyclonucleoside Phosphonates
Author:
Affiliation:
1. University of Orléans CNRS, ICOA UMR 7311, Orléans France
Publisher
Wiley
Subject
General Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/0471142700.nc1411s59
Reference28 articles.
1. Michaelis-Arbusow- und Perkow-Reaktionen
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4. Metathesis strategy in nucleoside chemistry
5. S-Adenosylhomocysteine Analogues with the Carbon-5‘ and Sulfur Atoms Replaced by a Vinyl Unit
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1. Synthesis of LAVR-289, a new [(Z)-3-(acetoxymethyl)-4-(2,4-diaminopyrimidin-6-yl)oxy-but-2-enyl]phosphonic acid prodrug with pronounced antiviral activity against DNA viruses;European Journal of Medicinal Chemistry;2024-05
2. Recent Synthesis of Nucleoside Phosphonate Analogs Using Olefin Cross-metathesis;Current Medicinal Chemistry;2024-04-30
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