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Ozonides of N-acyl-4-phenyl-3a,4,5,9b-tetrahydro-3H-cyclopenta [c]quinoline

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Abstract

Ozonation of N-acyl-4-phenyl-3a,4,5,9b-tetrahydro-3 H-cyclopenta[ c]quinoline gave stable ozonides: a conformationally mobile isomer with the pseudoequatorial N-acyl group and a conformationally stable isomer with the pseudoaxial N-trifluoroacetyl group.

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Authors and Affiliations

  1. Institute of Petrochemistry and Catalysis, Russian Academy of Sciences, 141 prosp. Oktyabrya, 450075, Ufa, Russian Federation

    A. G. Tolstikov, L. M. Khalilov, R. G. Savchenko & V. N. Odinokov

  2. Institute of Technical Chemistry, Ural Branch of the Russian Academy of Sciences, 3 ul. Akad. Koroleva, 614013, Perm, Russian Federation

    D. V. Nedopekin, V. A. Glushkov & G. F. Krainova

  3. A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 ul. Vavilova, 119991, Moscow, Russian Federation

    I. V. Glukhov & M. Yu. Antipin

Authors
  1. A. G. Tolstikov
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  2. L. M. Khalilov
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  3. R. G. Savchenko
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  4. D. V. Nedopekin
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  5. V. A. Glushkov
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  6. G. F. Krainova
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  7. I. V. Glukhov
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  8. M. Yu. Antipin
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  9. V. N. Odinokov
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Corresponding author

Correspondence to V. N. Odinokov.

Additional information

Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 9, pp. 1929–1933, September, 2009.

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Tolstikov, A.G., Khalilov, L.M., Savchenko, R.G. et al. Ozonides of N-acyl-4-phenyl-3a,4,5,9b-tetrahydro-3H-cyclopenta [c]quinoline. Russ Chem Bull 58, 1991–1995 (2009). https://doi.org/10.1007/s11172-009-0272-3

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  • DOI: https://doi.org/10.1007/s11172-009-0272-3

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