Synthesis and Antiviral Evaluation of Pyrazinones Substituted with Acyclic Chains
The synthesis of a series of pyrazine analogues of the anti-herpes compound, acyclovir is described. These syntheses were accomplished by various methods: in the presence of a Lewis acid or NaH for hydroxyethoxymethyl and hydroxybutyl groups or by sequential oxidation/reduction of l-β-D-ribofuranosy...
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Veröffentlicht in: | Nucleosides & nucleotides 1998-05, Vol.17 (5), p.875-892 |
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Sprache: | eng |
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