Abstract
1-Nucleosides of 5-substituted 4-chloro-1,2,3-triazoles were produced by glycosylation of the corresponding triazoles by the method of fusion with tetra-0-acyl-D-ribofuranose in the presence of bis-p-nitrophenyl phosphate. The structure of the compounds obtained and their conformational peculiarities were studied by the methods of mass spectrometry and NMR spectroscopy.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 11, pp. 1556–1564, November, 1984.
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Shingarova, I.D., Yartseva, I.V., Nemeryuk, M.P. et al. 1-Nucleosides of 5-substituted 4-chloro-1,2,3-triazoles. Chem Heterocycl Compd 20, 1287–1294 (1984). https://doi.org/10.1007/BF00505724
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DOI: https://doi.org/10.1007/BF00505724