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Reactions of cyclic ammonium cations

VII. Quinolination of 1-alkyl-2,3-dihydroindoles and 1-alkyl-1,2,3,4-tetrahydroquinolines

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

A method for the introduction of a quinoline residue into an aromatic ring by means of 1-acylquinolinium salts was developed. The effect of the anion was examined. A number of quinolylindoles and quinolyltetrahydroquinolines were synthesized by this method. It is shown that electron-acceptor or electron-donor substituents in the benzene ring of the quinolinium salt have practically no effect on the course of the process.

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Authors and Affiliations

  1. Donets State University, USSR

    A. K. Sheinkman, A. N. Prilepskaya & A. N. Kost

  2. M. V. Lomonosov Moscow State University, USSR

    A. K. Sheinkman, A. N. Prilepskaya & A. N. Kost

Authors
  1. A. K. Sheinkman
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  2. A. N. Prilepskaya
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  3. A. N. Kost
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Additional information

See [1] for Communication VI.

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 11, pp. 1515–1521, November, 1970.

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Sheinkman, A.K., Prilepskaya, A.N. & Kost, A.N. Reactions of cyclic ammonium cations. Chem Heterocycl Compd 6, 1413–1419 (1970). https://doi.org/10.1007/BF00476785

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  • DOI: https://doi.org/10.1007/BF00476785

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