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The structure of regalamine

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On the basis of UV, IR, NMR, and mass spectra and chemical transformations the structure of 11,12-dihydroxy-2-methoxy-1,12-epoxyhexahydrohomoproaporphine has been proposed for regalamine.

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Literature cited

  1. 1.

    M. K. Yusupov and A. S. Sadykov, Zh. Obshch. Khim.,34, 1672 (1964).

  2. 2.

    M. K. Yusupov, in: The Chemistry of Plant Substances [in Russian], Tashkent (1972), p. 19.

  3. 3.

    M. Ohashi, J. M. Wilson, H. Budzikewicz, M. Shamma, W. A. Slusarchyk, and C. Djerassi, J. Amer. Chem. Soc.,85, 2807 (1963).

  4. 4.

    M. Baldwin, A. J. Loudon, A. Maccoll, L. J. Haynes, and K. L. Stuart, J. Chem. Soc., C., 154 (1967).

  5. 5.

    T. Reichstein, G. Snatzke, and F. Šantavý, Planta Med.,16, 357 (1968).

  6. 6.

    F. Šantavý, P. Sedmera, G. Snatzke, and T. Reichstein, Helv. Chim. Acta,54, 1084 (1971).

  7. 7.

    F. Šantavý, in: The Chemistry of Plant Substances [in Russian], Tashkent (1972), p. 7.

  8. 8.

    F. A. Anet and A. J. R. Bourn, J. Amer. Chem. Soc.,87, 5250 (1965).

  9. 9.

    K. L. Stuart and M. P. Cava, Chem. Rev.,68, 321 (1968).

  10. 10.

    A. P. Orekhov, The Chemistry of the Alkaloids [in Russian], Moscow (1955).

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Additional information

V. I. Lenin Tashkent State University. Translated from Khimiya Prirodnykh Soedinenii, No. 3, pp. 383–387, May–June, 1975.

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Yusupov, M.K., Abdullaeva, D.A., Aslanov, K.A. et al. The structure of regalamine. Chem Nat Compd 11, 395–397 (1975). https://doi.org/10.1007/BF00571217

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  • Alkaloid
  • Acetyl Chloride
  • Hydrogen Chloride
  • Tetrahydroisoquinoline
  • Methiodide