Abstract
Mass fragmentation of 2-hydrazono-1,3-thiazolidin-4-ones is dominated by two processes, namely cleavage of the hydrazone fragment with accompanying proton transfer from the latter to the thiazolidine ring, and cleavage of a hydrazone imide residue.
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Literature Cited
E. Winterfeldt and J. M. Nelke, Chem. Ber., 100, 3671 (1967).
J. W. Lown and J. C. N. Ma, Can. J. Chem., 45, 939 (1967).
H. Nagase, Chem. Pharm. Bull., 21, 270 (1973).
R. M. Acheson and J. D. Wallis, J. Chem. Soc., Perkin 1, No. 2, 415 (1981).
V. Ya. Kauss, É. É. Liepin'sh, I. Ya. Kalvin'sh, and É. Lukevits, Khim. Geterotsikl. Soedin., No. 1, 120 (1990).
L. I. Giannola, G. Giammona, S. Palazzo, and L. Lamartina, J. Chem. Soc., Perkin 1, No. 12, 2707 (1984).
A. F. Cameron, N. J. Nair, N. F. Elmore, and P. J. Taylor, Chem. Commun., No. 14, 890 (1970).
E. Adman, L. H. Jensen, and R. N. Warrener, Acta Cryst., B31, 1915 (1975).
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 8, pp. 1117–1119, August, 1990.
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Kauss, V.Y., Rozite, S.K., Mazheika, I.B. et al. Electron impact mass spectra of 2-hydrazono-1,3-thiazolidin-4-one derivatives. Chem Heterocycl Compd 26, 935–937 (1990). https://doi.org/10.1007/BF00480875
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DOI: https://doi.org/10.1007/BF00480875