Skip to main content
Log in

Hydroacridines and related compounds

XIV. Reductive properties of some N-aryldecahydroacridines

  • Published:
Chemistry of Heterocyclic Compounds Aims and scope

Abstract

Some N-aryldecahydroacridines reduce N=N, C=N, C=O, NO2, and acridine groups in acidic media. In neutral media, N-aryldecahydroacridines are oxidized by caloranil and polyhaloalkanes.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Literature cited

  1. G. A. Klimov, A. V. Krivenkova, T. N. Makar'eva, and M. N. Tilichenko, Khim. Geterotsikl. Soedin., 824 (1973).

  2. E. A. Braude, I. Hannah, and S. R. Linstead, J. Chem. Soc., 3251 (1960).

  3. I. L. Kurz, R. F. Hutton, and F. H. Westheimer, J. Amer. Chem. Soc., 83, 584 (1961).

    Google Scholar 

  4. A. N. Saverchenko, V. A. Kaminskii, and M. N. Tilichenko, Khim. Geterotsikl. Soedin., 384 (1973).

  5. D. N. Kursanov and Z. I. Parnes, Usp. Khim., 38, 1783 (1969).

    Google Scholar 

  6. V. A. Kaminskii, A. N. Saverchenko, and M. N. Tilichenko, Khim. Geterotsikl. Soedin., 1538 (1970).

  7. V. A. Kaminskii, A. N. Saverchenko, and M. N. Tilichenko, Zh. Organ. Khim., 6, 404 (1970).

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

See [1] for communication XIII.

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 6, pp. 809–811, June, 1974

Rights and permissions

Reprints and permissions

About this article

Cite this article

Saverchenko, A.N., Kaminskii, V.A. & Tilichenko, M.N. Hydroacridines and related compounds. Chem Heterocycl Compd 10, 702–704 (1974). https://doi.org/10.1007/BF00480930

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00480930

Keywords

Navigation