Acylation of 3-methyl-2-azafluorene

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. © 1977 Plenum Publishing Corporation.

Authors
Prostakov N.S. 1 , Mokhomon K.M.S.1 , Gaivoronskaya L.A. 1 , Kesarev O.G.1 , Savina A.A. 1
Journal
Chemistry of Heterocyclic Compounds
Publisher
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Number of issue
7
Language
English
Pages
798-801
Status
Published
Link
External link
DOI
10.1007/BF00477016
Volume
12
Year
1977
Organizations
  • 1 Patrice Lumumba International Friendship University, Moscow, Russian Federation
Date of creation
19.10.2018
Date of change
19.10.2018
Short link
https://repository.rudn.ru/en/records/article/record/1680/
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MASS SPECTROMETRIC STUDY OF 2-AZAFLUORENES

Article
Zvolinskii V.P., Zakharov P.I., Shevtsov V.K., Pleshakov V.G., Varlamov A.V., Vasil'ev G.A., Furnaris K.I., Prostakov N.S.
Chemistry of Heterocyclic Compounds. Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau. Vol. 13. 1977. P. 86-90