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

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. © 1975 Plenum Publishing Corporation.

Authors
Prostakov N.S. 1 , Ismailov A.Ya.1 , Zvolinskii V.P. 1
Publisher
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Number of issue
7
Language
English
Pages
907-910
Status
Published
Volume
9
Year
1975
Organizations
  • 1 Patrice Lumumba 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/1744/
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