Schiff bases in syntheses of substituted naphthylamines, naphthyridines, azaphenanthrenes, and benzocarbazole

9-Methylnaphtho[2,1-b][1,6]naphthyrldine and 2,3-dimethyl-1-azaphenanthrene were obtained on a K-16 dehydrogenating catalyst from N-(1,2,5-trimethyl-4-piperidylidene)-β-naphthylamine, while N-cyclohexylidene-α-naphthylamine yielded N-phenyl-α-naphthylamine and benzo[a]carbazole. © 1974 Consultants Bureau.

Authors
Prostakov N.S. 1 , Pleshakov V.G. 1 , Kholdarova T.1 , Zvolinskii V.P. 1 , Plaksii L.N.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
1264-1267
Status
Published
Link
External link
DOI
10.1007/BF00475545
Volume
8
Year
1974
Organizations
  • 1 P. 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/1833/
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BENZYLATION OF 2,5-DIMETHYL-4-PHENYL(P-ALKYLBENZYL) PYRIDINES

Article
Prostakov N.S., Moiz S.S., Zvolinskii V.P., Dorogov V.V.
Chemistry of Heterocyclic Compounds. Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau. Vol. 8. 1974. P. 85-88