Abstract
The principal pathways of the fragmentation of 2-methylnitroindolizines were investigated. The fragmentation and structures of the isomeric [M-OH]+ and [M-NO]+ ions formed in the fragmentation of these compounds were studied by the method of dissociative activation by collision (DAC). It was established that the stable [M-OH]+ ions formed in the fragmentation of the 1- and 3-nitro isomers as a result of the “ortho effect” have different structures and that their DAC spectra can be used to determine the position of the nitro group in the molecule.
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M. S. Bobyleva and N. S. Kulikov, Teor. éksp. Khim. (1989).
O. A. Solov'ev, Master's Dissertation, Izd. Moskovsk. Gosudarstv. Univ., Moscow (1975).
P. B. Terent'ev, O. A. Solov'ev, R. A. Khmel'nitskii, S. P. Gromov, and R. S. Sagitullin, Khim. Geterotsikl. Soedin., No. 6, 765 (1982).
S. I. Bobrovskii, E. V. Babaev, and Yu. G. Bundel', Vestnik Moskovsk. Gosudarstv. Univ., Ser. 2, Khim., 26, 222 (1985).
R. A. Khmel'nitskii and P. B. Terent'ev, Usp. Khim., 48, 854 (1979).
N. S. Vul'fson, V. G. Zaikin, and A. I. Mikaya, Mass Spectrometry of Organic Compounds [in Russian], Khimiya, Moscow (1986), p. 312.
A. N. Kost, R. S. Sagitullin, and S. P. Gromov, Khim. Geterotsikl. Soedin., No. 7, 922 (1976).
E. T. Borrows, D. O. Holland, and J. Kenyon, J. Chem. Soc., 1077 (1946).
J. A. Hickman and D. G. Wibberley, J. Chem. Soc., Perkin 1, 2954 (1972).
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 12, pp. 1631–1635, December, 1988.
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Bobyleva, M.S., Kulikov, N.S. & Bobrovskii, S.I. Mass spectrometry and structures of ions of heterocyclic compounds activated by collision. 2. 2-Methylnitroindolizines. Chem Heterocycl Compd 24, 1347–1351 (1988). https://doi.org/10.1007/BF00486677
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DOI: https://doi.org/10.1007/BF00486677