Abstract
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.
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Cho, Y.H., Yang, JW., Chun, B.K. et al. Synthesis of acyclonucleosides (4). Arch. Pharm. Res. 12, 300–305 (1989). https://doi.org/10.1007/BF02911064
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DOI: https://doi.org/10.1007/BF02911064