Synthesis, structure, and biological activity of [2.2]paracyclophanes. 7. Synthesis of 2-([2.2]paracyclophan-4-yl)pyridines, -tetrahydroquinolines, and -benzo[h]quinolines based on condensation of 4-(β-dimethylaminopropionyl)[2.2]paracyclophane with primary amines

Condensation of 4-(β-dimethylaminopropionyl)paracyclophane with aliphatic aldehydes or cyclohexanones in the presence of hydroxylamine gave 2-([2.2]paracyclophan-4-yl)pyridines and -5,6,7,8-tetrahydroquinolines respectively. Reaction of these salts with α-naphthylamine gives a mixture of paracyclophanyl substituted 1,2,3,4-tetrahydrobeno[h]quinoline and benzo[h]quinoline. ©1998 Plenum Publishing Corporation.

Authors
Kryvenko L.I. 1 , Soldatova S.A. 1 , Zvolinskii O.V. 1 , Romanenko É.É.1 , Struchkova M.I.1 , Soldatenkov A.T. 1
Editors
-
Publisher
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Number of issue
8
Language
English
Pages
933-936
Status
Published
Department
-
Number
-
Volume
33
Year
1997
Organizations
  • 1 Russian University of National Friendship, 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/743/