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Mass-spectrometric study of 6-methyl-2-aryl-7-benzylindolizines

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The mass-spectral behavior of 15 compounds from the 6-methyl-2-aryl-7-benzylindolizine series was investigated, and it was shown that the peculiarities of their dissociative ionization are due to the formation of stable resonance-stabilized ions that contain a quaternized nitrogen atom in the heteroring.

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Authors and Affiliations

  1. Patrice Lumumba Peoples' Friendship University, 117923, Moscow

    P. I. Zakharov, V. P. Zvolinskii, I. Romero Maldonado, B. N. Anisimov, A. T. Soldatenkov, A. P. Krapivko, V. I. Kuznetsov & N. S. Prostakov

Authors
  1. P. I. Zakharov
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  2. V. P. Zvolinskii
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  3. I. Romero Maldonado
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  4. B. N. Anisimov
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  5. A. T. Soldatenkov
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  6. A. P. Krapivko
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  7. V. I. Kuznetsov
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  8. N. S. Prostakov
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Additional information

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 10, pp. 1368–1373, October, 1981.

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Zakharov, P.I., Zvolinskii, V.P., Romero Maldonado, I. et al. Mass-spectrometric study of 6-methyl-2-aryl-7-benzylindolizines. Chem Heterocycl Compd 17, 1025–1030 (1981). https://doi.org/10.1007/BF00503533

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  • DOI: https://doi.org/10.1007/BF00503533

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