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9-Phenyl-10-alkyl(aryl)perhydroacridines from 9-phenyl-10-alkyl(aryl)decahydroacridines

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

9-Phenyldecahydroacridines with a substituent in the 10 position are reduced stereospecifically to the corresponding perhydroacridines by treatment with formic acid or a mixture of dimethylformamide and concentrated HCl. Perhydroacridines are also formed by disproportionation of the corresponding decahydroacridines.

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Literature cited

  1. A. N. Saverchenko, V. A. Kaminskii, and M. N. Tilichenko, Khim. Geterotsikl. Soedin., No. 3, 384 (1973).

    Google Scholar 

  2. A. N. Saverchenko, Z. R. Bekkerova, V. A. Kaminskii, and M. N. Tilichenko, Khim. Geterotsikl, Soedin., No. 2, 243 (1974).

    Google Scholar 

  3. V. I. Alekseev, V. A. Kaminskii, and M. N. Tilichenko, Khim. Geterotsikl. Soedin., No. 2, 235 (1975).

    Google Scholar 

  4. U. Eisner and J. Cuthan, Chem. Rev., 72, 1 (1972).

    Google Scholar 

  5. N. Bărbulescu and F. Potmichil, Rev. Roum. Chim., 15, 1601 (1970).

    Google Scholar 

  6. V. G. Dashevskii, Conformations of Organic Molecules [in Russian], Khimiya, Moscow (1974), p. 189.

    Google Scholar 

  7. A. Zhunke, Nuclear Magnetic Resonance in Organic Chemistry [in Russian], Mir, Moscow (1974), p. 30.

    Google Scholar 

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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 7, pp. 957–962, July, 1976.

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Alekseev, V.I., Kaminskii, V.A. & Tilichenko, M.N. 9-Phenyl-10-alkyl(aryl)perhydroacridines from 9-phenyl-10-alkyl(aryl)decahydroacridines. Chem Heterocycl Compd 12, 793–797 (1976). https://doi.org/10.1007/BF00477015

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  • DOI: https://doi.org/10.1007/BF00477015

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