N-oxides of 2- and 4-azafluorenones and nitro derivatives of 2- and 4-azafluorenes

It was demonstrated by PMR spectroscopy that mixtures of N-oxides of 6- and 7-nitro derivatives are formed in the nitration of the N-oxides of 3-methyl-2- and 4-azafluorenes. The products were deoxygenated to give nitro derivatives of 2- and 4-azafluorenes. The N-oxides of nitro-substituted azafluorenes were converted to salts of the aci forms by the action of alkali. © 1983 Plenum Publishing Corporation.

Authors
Prostakov N.S. 1 , Shendrik I.V. 1 , Anisimov B.N. 1 , Varlamov A.V. 1 , Fomichev A.A. 1 , Lavani-Édogiaverie S. 1
Journal
Chemistry of Heterocyclic Compounds
Publisher
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Number of issue
10
Language
English
Pages
1085-1088
Status
Published
Link
External link
DOI
10.1007/BF00503201
Volume
18
Year
1982
Organizations
  • 1 Patrice Lumumba Peoples' Friendship University, Moscow, 117923, Russian Federation
Date of creation
19.10.2018
Date of change
19.10.2018
Short link
https://repository.rudn.ru/en/records/article/record/1448/
Share

Other records

ELECTROPHILIC SUBSTITUTION OF 1-METHYLINDENO-1H-[2,1-B]PYRIDINE

Article
Prostakov N.S., Soldatenkov A.T., Bagdadi M.V., Fomichev A.A., Golovtsov N.I.
Chemistry of Heterocyclic Compounds. Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau. Vol. 18. 1982. P. 954-956