Synthesis of 5-substituted 2'-deoxyuridine-5'- phosphonate analogues and evaluation of their antiviral activity
Sara Van Poecke1, Davy Sinnaeve, José C Martins
1Laboratory for Medicinal Chemistry, Faculty of Pharmaceutical Sciences, Ghent University, Gent, Belgium.
Nucleosides, Nucleotides & Nucleic Acids
|February 24, 2012
Abstract:
A small series of 5-(hetero)aryl-modified nucleoside phosphonates was synthesized via an 8-step procedure including a Wittig reaction and Suzuki-Miyaura coupling. An unanticipated anomerization during phosphonate deprotection allowed us to isolate both anomers of the 5-substituted 2'-deoxy-uridine phosphonates and assess their antiviral activity against a broad panel of viruses.
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