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.
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Additional information
Russian Peoples' Friendship University, Moscow 117198. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 1, pp. 99–104, January, 1997.
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Zvolinskii, O.V., Kryvenko, L.I., Sergeeva, N.D. et al. Synthesis and structure of 2-aryl-2,4-dimethyl-1,2,3,4-tetrahydroquinolines and 1,3-disubstituted indenes. Chem Heterocycl Compd 33, 86–90 (1997). https://doi.org/10.1007/BF02290752
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DOI: https://doi.org/10.1007/BF02290752