Abstract
2-Β-D-Ribofuranosyl-4-methylthio-5-methoxycarbonyl-1,2,3-triazole was obtained by fusing 4-methylthio-5-methoxycarbonyl-1,2,3-triazole together with tetraacyl-D-ribofuranose, followed by deacylation, and its amide and hydrazide were prepared. The structures of the new nucleosides were established by converting them into known 2-nucleosides of 1,2,3-triazol-4-yl-carboxylic acid derivatives.
This is a preview of subscription content, log in via an institution to check access.
Similar content being viewed by others
Literature cited
M. N. Preobrazhenskaya and S. Ya. Mel'nik, Analogs of Nucleic Acid Components — Nucleic Acid Metabolism Inhibitors, Progress in Science, Bioorganic Chemistry Series [in Russian], Vol. 1, VINITI, Moscow (1984), p. 180.
M. P. Nemeryuk, A. L. Sedov, and T. S. Safonova, Third Moscow Conference on Organic Chemistry and Technology, Summaries of Lectures [in Russian], Moscow (1982), p. 72.
F. A. Lehmkuhl, J. T. Witkowski, and R. K. Robins, J. Heterocycl. Chem.,9, 1195 (1972).
G. Alonso, M. T. Garcia-Lopez, G. Garcia-Munoz, R. Mandronero, and M. Rico, J. Heterocycl. Chem.,7, 1269 (1970).
Author information
Authors and Affiliations
Additional information
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 2, pp. 231–235, February, 1987.
Rights and permissions
About this article
Cite this article
Shingarova, I.D., Yartseva, I.V. & Preobrazhenskaya, M.N. Nucleosides of 4-methylthio-1,2,3-triazol-5-yl-carboxylic acid derivatives. Chem Heterocycl Compd 23, 194–198 (1987). https://doi.org/10.1007/BF00663860
Received:
Issue Date:
DOI: https://doi.org/10.1007/BF00663860