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Reaction of hexafluoroacetone with azacyclohexanes

  • Organic Chemistry
  • Published:
Bulletin of the Academy of Sciences of the USSR, Division of chemical science Aims and scope

Conclusions

Piperidine and its C-methyl derivatives are aromatized by hexafluoroacetone with simultaneous C-alkylation at one or both of the Β-positions of the ring, and in the case of α- and γ-methylpyridines also at the CH3 group.

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Literature cited

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Authors and Affiliations

  1. A. N. Nesmeyanov Institute of Organoelemental Chemistry, Academy of Sciences of the USSR, Moscow

    V. D. Sviridov, N. D. Chkanikov, M. V. Galakhov, A. F. Kolomiets & A. V. Fokin

Authors
  1. V. D. Sviridov
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  2. N. D. Chkanikov
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  3. M. V. Galakhov
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  4. A. F. Kolomiets
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  5. A. V. Fokin
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Additional information

For previous communication, see [1].

Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 7, pp. 1652–1656, July, 1989.

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Sviridov, V.D., Chkanikov, N.D., Galakhov, M.V. et al. Reaction of hexafluoroacetone with azacyclohexanes. Russ Chem Bull 38, 1515–1518 (1989). https://doi.org/10.1007/BF00978449

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  • DOI: https://doi.org/10.1007/BF00978449

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