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Synthesis and tautomerism of 1-substituted 3,3-dialkyl-3,4-dihydroisoquinolines

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

A number of ethyl esters of 3,3-dialkyl-3,4-dihydroisoquinoline-Δ1(2H), α-α- alkylacetic acids have been synthesized. The effect of replacement of α-hydrogen by alkyl radicals on the azomethine-enamine tautomeric equilibrium was shown.

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Authors and Affiliations

  1. Institute of Flow Mechanics, Ural Scientific Center, Academy of Sciences of the USSR, 614600, Perm'

    B. B. Aleksandrov, M. S. Gavrilov, M. I. Vakhrin & V. S. Shklyaev

Authors
  1. B. B. Aleksandrov
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  2. M. S. Gavrilov
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  3. M. I. Vakhrin
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  4. V. S. Shklyaev
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Additional information

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 6, pp. 794–797, June, 1985.

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Aleksandrov, B.B., Gavrilov, M.S., Vakhrin, M.I. et al. Synthesis and tautomerism of 1-substituted 3,3-dialkyl-3,4-dihydroisoquinolines. Chem Heterocycl Compd 21, 662–665 (1985). https://doi.org/10.1007/BF00515067

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  • DOI: https://doi.org/10.1007/BF00515067

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