Synthesis of acyclonucleosides (4)
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The synthetic study of 3′-azido and 3′-fluoro secouridines toward development of new antiviral agents is described. These acyclic nucleosides were synthesized from, uridine by the method of ring opening reaction of sugar moiety.
KeywordsAcyclonucleoside fluorosecouridine azidosecouridine
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