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- W2034353546 abstract "This article describes an efficient route for synthesizing novel cyclopropyl homologous PMEA analogues. The condensation of the bromide 8 with nucleosidic bases (A, U, T, C, 5-FU, G) under standard nucleophilic substitution and deprotection conditions, afforded the target phosphonic acid analogues 14∼18 and 21. These compounds were evaluated for their potential antiviral properties against various viruses. Guanine derivative 21 showed significant antiviral activity." @default.
- W2034353546 created "2016-06-24" @default.
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- W2034353546 date "2008-01-18" @default.
- W2034353546 modified "2023-10-16" @default.
- W2034353546 title "Design, Synthesis and Anti-HIV Activity of Homologous PMEA Derivatives" @default.
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- W2034353546 doi "https://doi.org/10.1080/15257770701795953" @default.
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