Synthesis and structure of 2-aryl-2,4-dimethyl-1,2,3,4-tetrahydroquinolines and 1,3-disubstituted indenes

It has been shown that the intramolecular cyclization of N-(1-arylbutenyl)arylamines under acid catalysis conditions may proceed in two directions with the formation of 2-aryl-2,4-dimethyl-1,2,3,4-tetrahydroquinolines and 1,3 disubstituted indenes. ©1997 Plenum Publishing Corporation.

Authors
Zvolinskii O.V. 1 , Kryvenko L.I. 1 , Sergeeva N.D. 1 , Soldatenkov A.T. 1 , Prostakov N.S. 1
Journal
Chemistry of Heterocyclic Compounds
Publisher
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Number of issue
1
Language
English
Pages
86-90
Status
Published
Link
External link
DOI
10.1007/BF02290752
Volume
33
Year
1997
Organizations
  • 1 Russian Peoples' Friendship University, Moscow 117198, Russian Federation
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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

Article
Kryvenko L.I., Soldatova S.A., Zvolinskii O.V., Romanenko É.É., Struchkova M.I., Soldatenkov A.T.
Chemistry of Heterocyclic Compounds. Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau. Vol. 33. 1997. P. 933-936