Chemistry of Heterocyclic Compounds

, Volume 9, Issue 7, pp 907–910 | Cite as

9-Acyl- and 9-aroyl-3-methyl-2-azafluorenes

  • N. S. Prostakov
  • A. Ya. Ismailov
  • V. P. Zvolinskii


The condensation of 3-methyl-2-azafluorene with esters of aromatic and aliphatic acids has given 9-aroyl and 9-acyl derivatives of 2-azafluorene. They are stable in the enolic form. The 9-benzoyl derivative (II) has also been isolated in the oxo form. The transition from (II) to the cis-trans isomers of 9-benzylidene-3-methyl-2-azafluorene has been effected.


Ester Organic Chemistry Enolic Form Aliphatic Acid 
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.


Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

Literature cited

  1. 1.
    N. S. Prostakov, C. J. Matthew, and V. A. Kurichev, Khim. Geterotsikl. Soedin., 876 (1967).Google Scholar
  2. 2.
    L. Bellamy, Infra-red Spectra of Complex Molecules, 2nd ed., Methuen (1958).Google Scholar
  3. 3.
    K. Nakanishi, Infrared Spectroscopy. Practical, Holden-Day, San Francisco (1962).Google Scholar
  4. 4.
    N. S. Prostakov, S. S. Moiz, A. T. Soldatenkov, V. P. Zvolinskii, and G. I. Cherenkova, Khim. Geterotsikl. Soedin., 1398 (1971).Google Scholar
  5. 5.
    E. J. Greenhow, D. McNeil, and E. N. White, J. Chem. Soc., 986 (1952).Google Scholar

Copyright information

© Plenum Publishing Corporation 1975

Authors and Affiliations

  • N. S. Prostakov
    • 1
  • A. Ya. Ismailov
    • 1
  • V. P. Zvolinskii
    • 1
  1. 1.Patrice Lumumba UniversityMoscow

Personalised recommendations