Abstract
A trans configuration with an axial orientation of both the purine ring and the furyl ring or the ethoxy group in the 2 position of the dioxane residue was established by PMR spectroscopy for 9-(2-furyl-1,3-dioxan-5-yl)- and 9-(2-ethoxy-2-methyl-1,3-dioxan-5-yl)purine. A comparative analysis of the mass spectra of these compounds makes it possible to confirm conclusions regarding their stereochemistry drawn on the basis of the PMR spectra.
Similar content being viewed by others
Literature cited
A. F. Mishnev, Ya. Ya. Bleidelis, É. É. Liepin'sh, N. P. Ramzaeva, and I. N. Goncharova, Khim. Geterotsikl. Soedin., No. 7, 976 (1979).
Yu. Yu. Samitov, I. N. Goncharova, N. P. Ramzaeva, A. F. Mishnev, and Ya. Ya. Bleidelis, Khim. Geterotsikl. Soedin., No. 11, 1523 (1981).
V. G. Zaikin and N. S. Vul'fson, Khim. Geterotsikl. Soedin., No. 11, 1443 (1978).
A. Mandelbaum, Mass Spectrometry Rev., 2, 223 (1983).
J. Reuben, Prog. NMR Spectrosc., 9, 7 (1973).
Yu. Yu. Samitov, Atlas of the NMR Spectra of Spatial Isomers [in Russian], Vol. 1, Izd. Kazansk. Univ. (1978), p. 100.
N. A. Klyuev, I. S. Shpileva, L. I. Medvedeva, G. N. Lyapunova, and N. P. Bednyagina, Khim. Geterotsikl. Soedin., No. 11, 1506 (1981).
I. L. Holmes and F. P. Lossing, Org. Mass Spectrom., 14, 512 (1979).
Author information
Authors and Affiliations
Additional information
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 5, pp. 691–696, May, 1984.
Rights and permissions
About this article
Cite this article
Samitov, Y.Y., Goncharova, I.N., Ramzaeva, N.P. et al. Mass-spectrometric behavior and PMR spectra of 9-(2-R-1,3-dioxan-5-yl)purines. Chem Heterocycl Compd 20, 558–564 (1984). https://doi.org/10.1007/BF00514312
Received:
Issue Date:
DOI: https://doi.org/10.1007/BF00514312