Chemistry of Heterocyclic Compounds p. 769 - 772 (1987)
Update date:2022-09-26
Topics:
Shingarova, I. D.
Lebedev, A. T.
Preobrazhenskaya, M. N.
The structure of previously obtained nucleosides of 5-substituted 4-chloro-1,2,3-triazoles were refined by means of high-resolution mass spectrometry and 13C NMR spectroscopy.It is shown that fusion of 5-substituted 4-chloro 1,2,3-triazoles with tetra-O-acylribofuranoses in the presence of di(p-nitrophenyl)phosphate leads to the formation of 2-nucleosides of the corresponding triazoles.The signals of the carbon atoms in the 13C NMR spectra of the 4,5-di-substituted triazoles and their nucleosides were assigned.
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Doi:10.1021/jm00388a006
(1987)Doi:10.1039/c39860001170
(1986)Doi:10.1016/0040-4020(86)80018-7
(1986)Doi:10.1055/s-2008-1077885
(2008)Doi:10.5935/0103-5053.20130276
(2014)Doi:10.1021/ic801221r
(2008)