Abstract
The mass spectra of eight alkyl- and dialkylamino-substituted oxazolino- and thiazolino-sym-triazines were investigated. It is shown that prior to fragmentation with opening of the oxazoline ring, the excited molecular ions of oxazolino-sym-triazines undergo rearrangement to N-vinyl-substituted sym-triazinols, The dissociative ionization of thiazolino-sym-triazines is primarily due to cleavage of the bonds in the thiazoline ring.
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R. G. Mirzoyan, S. M. Saakyan, A. V. Dovlatyan, and V. V. Dovlatyan, Arm. Khim. Zh., 32, 874 (1979).
V. V. Dovlatyan, K. A. Éliazyan, and A. V. Dovlatyan, Khim. Geterotsikl. Soedin., No. 7, 989 (1977).
V. V. Dovlatyan, A. V. Dovlatyan, K. A. Éliazyan, and R. G. Mirzoyan, Khim. Geterotsikl. Soedin., No. 10, 1420 (1977).
V. V. Dovlatyan and A. V. Dovlatyan, Khim. Geterotsikl. Soedin., No. 1, 124 (1979).
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 1, pp. 124–128, January, 1982.
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Mirzoyan, R.G., Saakyan, S.M., Demirchyan, M.P. et al. Mass-spectral investigation of some alkyl- and dialkylamino-substituted oxazolino- and thiazolino-sym-triazines. Chem Heterocycl Compd 18, 106–109 (1982). https://doi.org/10.1007/BF00513301
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DOI: https://doi.org/10.1007/BF00513301