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Reactions of 1,2-dihydroquinolines

IV. Reaction of 2,2,4-trimethyl-1,2-dihydroquinolines with cyclohexane

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

Under the Influence of anhydrous aluminum chloride, cyclohexane converts 2,2,4-trimethyl-1,2-dihydroquinoline to the tetrahydro derivative and alkylates it at the 7-position with simultaneous reduction of the Δ3-bond.

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Literature cited

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Authors and Affiliations

  1. M. V. Lomonosov Moscow State University, USSR

    B. A. Lugovik, P. V. Borodin, L. G. Yudin, V. A. Budylin & A. N. Kost

Authors
  1. B. A. Lugovik
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  2. P. V. Borodin
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  3. L. G. Yudin
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  4. V. A. Budylin
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  5. A. N. Kost
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Additional information

See [1] for communication III.

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 7, pp. 977–980, July, 1971.

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Lugovik, B.A., Borodin, P.V., Yudin, L.G. et al. Reactions of 1,2-dihydroquinolines. Chem Heterocycl Compd 7, 912–915 (1971). https://doi.org/10.1007/BF00475725

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  • DOI: https://doi.org/10.1007/BF00475725

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