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Chemistry of Heterocyclic Compounds

, Volume 12, Issue 7, pp 798–801 | Cite as

Acylation of 3-methyl-2-azafluorene

  • N. S. Prostakov
  • Kamara Maiga Sarata Mokhomon
  • L. A. Gaivoronskaya
  • O. G. Kesarev
  • A. A. Savina
Article

Abstract

Acylation of 3-methyl-2-azafluorene under various conditions yielded the enol forms of its (C(9) acyl derivatives, whereas the ketol form was also isolated in the case of the p-nitrobenzoyl derivative. The character of the compounds formed in the reaction of 3-methyl-2-azafluorene with benzoyl chloride and acetic anhydride is discussed.

Keywords

Acetic Chloride Organic Chemistry Anhydride Benzoyl 
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.

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Literature cited

  1. 1.
    N. S. Prostakov, A. Ya. Ismailov, and V. P. Zvolinskii, Khim. Geterotsikl. Soedin., No. 7, 986 (1973).Google Scholar
  2. 2.
    N. S. Prostakov, K. J. Mat'yu, and V. A. Kurichev, Khim. Geterotsikl. Soedin., No. 5, 876 (1967).Google Scholar

Copyright information

© Plenum Publishing Corporation 1977

Authors and Affiliations

  • N. S. Prostakov
    • 1
  • Kamara Maiga Sarata Mokhomon
    • 1
  • L. A. Gaivoronskaya
    • 1
  • O. G. Kesarev
    • 1
  • A. A. Savina
    • 1
  1. 1.Patrice Lumumba International Friendship UniversityMoscow

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