Advertisement

Chemistry of Heterocyclic Compounds

, Volume 20, Issue 4, pp 394–398 | Cite as

Pyrroloquinolines and pyrroloisoquinolines. 3. Synthesis of 1H-pyrrolo[2,3-f]isoquinoline and some of its derivatives

  • T. F. Ponasenkova
  • R. N. Akhvlediani
  • L. N. Kurkovskaya
  • V. V. Dikopolova
  • N. N. Suvorov
Article

Abstract

The preparative synthesis of 1H-pyrrolo[2,3-f]isoquinoline is proposed. Electrophilic substitution reactions, viz., the Mannich and Vilsmeier reactions and diazo coupling, were studied for the first time in the pyrroloisoquinoline series.

Keywords

Organic Chemistry Substitution Reaction Isoquinoline Electrophilic Substitution Pyrroloquinolines 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

Literature cited

  1. 1.
    A. P. Gryaznov, R. N. Akhvlediani, T. A. Volodina, A. M. Vasil'ev, T. A. Babushkina, and N. N. Suvorov, Khim. Geterotsikl. Soedin., No. 3, 369 (1977).Google Scholar
  2. 2.
    T. R. Covindachari and V. Rajappa Sudarsanam, Indian J. Chem., 4, 118 (1966).Google Scholar
  3. 3.
    T. R. Covindachariand V. Sudarsanam, Indian J. Chem., 5, 16 (1967).Google Scholar
  4. 4.
    T. R. Covindachari and V. Sudarsanam, Indian J. Chem., 7, 402 (1971).Google Scholar
  5. 5.
    C. G. Le Fevre and R. J. W. Le Fevre, J. Chem. Soc., No. 10, 1470 (1935).Google Scholar
  6. 6.
    H. F. Manske and M. Kulka, Can. J. Res., 27B, 161 (1949).Google Scholar
  7. 7.
    C. Kinast and L.-F. Teitze, Angew. Chem., 88, 261 (1976).Google Scholar
  8. 8.
    A. A. Polyakova and R. A. Khmel'nitskii, Mass Spectrometry in Organic Chemistry [in Russian], Khimiya, Leningrad (1972), p. 266.Google Scholar

Copyright information

© Plenum Publishing Corporation 1984

Authors and Affiliations

  • T. F. Ponasenkova
    • 1
  • R. N. Akhvlediani
    • 1
  • L. N. Kurkovskaya
    • 1
  • V. V. Dikopolova
    • 1
  • N. N. Suvorov
    • 1
  1. 1.D. I. Mendeleev Moscow Chemical Technology InstituteMoscow

Personalised recommendations