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Synthesis of nucleosides of substituted 3-hydroxypyrazoles

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

N-Glucoside analogs of the antibiotic pyrazofurine were obtained by fusion of 3-hydroxy-4-ethoxycarbonylpyrazole with tetra-O-acetyl-ß-D-ribofuranose in the presence of iodine.

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Literature cited

  1. R. J. Suhadolnik, in: Nucleoslde Antibiotics, Wiley-Interscience, New York (1970), p. 390.

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  2. H. Dorn (in press).

  3. H. Dorn, J. Prakt. Chem., 319, 281 (1977).

    Google Scholar 

  4. C. Tapiero and J.-L. Imbach, in: Nucleic Acid Chemistry (L. B. Townsend and R. S. Tipson, eds.), Wiley, New York (1978), p. 1055.

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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 11, pp. 1512–1514, November, 1981.

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Blanko, F.F., Korbukh, I.A., Preobrazhenskaya, M.N. et al. Synthesis of nucleosides of substituted 3-hydroxypyrazoles. Chem Heterocycl Compd 17, 1102–1104 (1981). https://doi.org/10.1007/BF00506461

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  • DOI: https://doi.org/10.1007/BF00506461

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