Condensation of 4-azafluorenone and 9-phenacylidene-4-azafluorene with acetophenone. Synthesis of 3′-oxo-spiro-[4-azafluorene-9,1′-indane]

Condensation of 4-azafluorenone and 9-phenacylidene-4-azafluorene with acetophenone leads to the formation of 9,9-diphenacyl-4-azafluorene and 9-(1′,2′-dibenzoylethylidene)-4-azafluorene. The structures of these products were confirmed based on their spectral and chemical data. The conversion of 9,9-diphenacyl-4-azafluorene to 3′-oxo-spiro-[4-azafluorene-9,1′-indane] represents a novel method for the preparation of this heterocycle. © 1989 Plenum Publishing Corporation.

Publisher
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Number of issue
9
Language
English
Pages
1024-1027
Status
Published
Volume
24
Year
1988
Organizations
  • 1 P. Lumumba Peoples' 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/1244/
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Prostakov N.S., Kuznetsov V.V., Gaivoronskaya L.A., Murugova L.A., Stashenko E.E., Zakharov P.I.
Chemistry of Heterocyclic Compounds. Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau. Vol. 24. 1988. P. 887-891