Synthesis and nitration of 4,6(4,8)-dimethyl-4-methyl-6(8)-methoxy-1,2,3,4-tetrahydrospiro [quinoline-2-cyclohexanes]

The cydization of 1-allyl-1-arylaminocyclohexanes under conditions of acid catalysis afforded 1,2,3,4-tetrahydro-4-methylspiro [quinoline-2-cyclohexanes] methyl (methoxy)-substituted in the phenylene ring. Their mono- and dinitro derivatives were synthesized, and their structure was established. Propositions on the direction of the nitration reaction of these heterocyclic compounds were expressed. © 1994 Plenum Publishing Corporation.

Authors
Kuznetsov V.V. 1 , Pal'ma A. 1 , Aliev A.E.1 , Fernandes M.1 , Prostakov N.S. 1 , Varlamov A.V. 1
Editors
-
Publisher
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Number of issue
6
Language
English
Pages
671-675
Status
Published
Department
-
Number
-
Volume
29
Year
1993
Organizations
  • 1 Russian University of the Friendship of Peoples, Moscow, 117198, Russian Federation
Keywords
-
Date of creation
19.10.2018
Date of change
19.10.2018
Short link
https://repository.rudn.ru/en/records/article/record/996/