Conversions of 9-bromo(cyano)-4-azafluorenes and 1,2-di(4-azafluoren-9-yl)ethane under conditions of the Michael reaction

9-Bromo(cyano)-4-azaflourenes are converted to di(4-azafluorylidene-9) or 9,9-di (β-cyanoethyl)-4-azafluorene under the conditions of the Michael reaction (acrylonitrile, ethoxytrimethylphenylammonium), depending on the temperature. 1,2-Di(4-azafluoren-9-yl)ethane was synthesized, and its cyanoethylation was performed. © 1985 Plenum Publishing Corporation.

Authors
Prostakov N.S. 1 , Shalimov V.P. 1 , Montenegro Cordova G.B.
Publisher
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Number of issue
11
Language
English
Pages
1260-1262
Status
Published
Volume
20
Year
1984
Organizations
  • 1 P. Lumumba Peoples' Friendship University, Moscow, 117923, Russian Federation
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Other records

Prostakov N.S., Soldatenkov A.T., Bagdadi M.V., Brindkha O.S., Kuznetsov V.I., Rezakov V.A., Fomichev A.A.
Chemistry of Heterocyclic Compounds. Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau. Vol. 20. 1984. P. 1128-1132