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

Authors

  • О. В. Зволинский Russian University of National Friendship, Moscow 117198
  • Л. И. Крывенко Russian University of National Friendship, Moscow 117198
  • Н. Д. Сергеева Russian University of National Friendship, Moscow 117198
  • А. Т. Солдатенков Russian University of National Friendship, Moscow 117198
  • Н. C. Простаков Russian University of National Friendship, Moscow 117198

Abstract

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.

How to Cite
Zvolinskii, O. V.; Kryvenko, L. I.; Sergeeva, N. D.; Soldatenkov, A. T.; Prostakov, N. S. Chem. Heterocycl. Compd. 1997, 33, 86. [Khim. Geterotsikl. Soedin. 1997, 99.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF02290752

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Published

1997-01-25

Issue

No. 1 (1997)

Section

Original Papers