Springer Nature is making SARS-CoV-2 and COVID-19 research free. View research | View latest news | Sign up for updates

Improved method of converting cardenolide aldoximes into 10-cyano compounds

  • 20 Accesses

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

Literature cited

  1. 1.

    I. F. Makarevich, M. V. Mokrouz, L. Ya. Topchii, I. P. Kovalev, V. E. Sokolova, Yu. I. Gubin, N. P. Bublik, and V. A. Polyakov, Khim. Prir. Soedin., No. 5 (1983).

  2. 2.

    E. Vowinkel and J. Bartel, Chem. Ber.,272, No. 1, 46 (1974).

  3. 3.

    L. Fuchs, M. Wichtl, and H. Jachs, Arch. Pharm.,291, 193 (1958).

  4. 4.

    I. F. Makarevich, Khim. Prir. Soedin., 221 (1968).

Download references

Additional information

All-Union Scientific-Research Institute of the Chemistry and Technology of Medicinal Substances. Translated from Khimiya Prirodnykh Soedinenii, No. 2, pp. 251–252, March–April, 1984.

Rights and permissions

Reprints and Permissions

About this article

Cite this article

Makarevich, I.F., Mokrouz, M.V. Improved method of converting cardenolide aldoximes into 10-cyano compounds. Chem Nat Compd 20, 235–236 (1984). https://doi.org/10.1007/BF00579500

Download citation

Keywords

  • Organic Chemistry
  • Cardenolide
  • Aldoximes