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Mass spectra of substituted 1,2,3,4-tetrahydro-γ-carbolines

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The mass-spectral behavior of substituted 1,2,3,4-tetrahydro-γ-carbolines has been investigated. For the 4-unsubstituted or 4-monosubstituted compounds a characteristic process is the primary retrodiene decomposition of the molecular ion. More characteristic for 4,4-disubstituted compounds is the primary loss of a substituent from position 4.

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Literature cited

  1. H. Budzikiewlcz, C. Djerassi, and D. H. Williams, Structure Elucidation of Natural Products by Mass-Spectrometry, Vol. I: Alkaloids, Holden-Day (1964).

  2. V. I. Vysotskii, R. A. Khmel'nitskii, I. I. Grandberg, and V. A. Budylin, Izv. Timiryazev. Sel'skokh. Akad., 221 (1970).

  3. V. I. Vysotskii, R. A. Khmel'nitskii, and I. I. Grandberg, Izv. Timiryazev. Sel'skokh. Akad, 204 (1970).

  4. R. A. Khmel'nitskii, V. A. Vysotskii, and I. I. Grandberg, Zh. Organ. Khim., 5, 417 (1969).

    Google Scholar 

  5. R. T. Coutts and R. A. Locak, Org. Mass. Spectr., 3, 879 (1970).

    Google Scholar 

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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 8, pp. 1047–1049, August, 1973.

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Belikov, A.B., Terent'ev, P.B., Yurovskaya, M.A. et al. Mass spectra of substituted 1,2,3,4-tetrahydro-γ-carbolines. Chem Heterocycl Compd 9, 971–973 (1973). https://doi.org/10.1007/BF00471709

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  • DOI: https://doi.org/10.1007/BF00471709

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