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   <subfield code="a">Synthesis of substituted pyridine-2,4-dione nucleosides</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Joon Lee, Jeong Won, Jung Park, Chang Hwang, K. Chung, Eung Ryu]</subfield>
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   <subfield code="a">The syntheses of novel heterocyclic base modified pyrimidine nucleosides are described. 5,6-Dimethyl-4-hydroxy-3-methoxy-1-(β-D-ribofuranosyl)-2(1H)-pyridinone7 was synthesized by condensation of silylated 5,6-dimethyl-4-hydroxy-3-methoxy-2(1H)-pyridinone with β-D-ribofuranose-1-acetate-2,3,5-tribenzoate in dichloroethane in the presence of Lewis acid followed by debenzoylation. The 2,2′-anhydro-5,6-dimethyl-2-hydroxy-3-methoxy-1-β-D-arabinofuranosyl-4-pyridinone8 was obtained from the reaction of the free ribonucleoside7 and diphenyl carbonate in DMF. None of these compounds showed any significant antiviral and antitumor activitiesin vitro tests.</subfield>
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