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The positions of the acyl groups in germerine and germitrine

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Summary

The positions of the acyl residues at C3 and C15 in germerine and germitrine have been corrected, showing that germerine is 3-(d)-2′-hydroxy-2′-methylbutyryl-15-(l)-2′-methylbutyrylgermine and germitrine is 7-acetyl-3-(d)-2′-hydroxy-2′-methylbutyryl-15-(l)-2′-methylbutyrylgermine.

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Literature cited

  1. S. M. Kupchan, J. Pharm. Sci.,50, 273 (1961).

    Article  CAS  Google Scholar 

  2. J. Fried, H. L. White, and O. Wintersteiner, J. Amer. Chem. Soc.,72, 4621 (1950).

    Article  CAS  Google Scholar 

  3. A. L. Shinkarenko and N. V. Bondarenko, Rast. Res.,2, 45 (1966).

    CAS  Google Scholar 

  4. N. V. Bondarenko, A. L. Shinkarenko, and G. I. Gerashchenko, Tr. Vitebskogo Tekhnologicheskogo Instituta Legkoi Promyshlennosti, 1, 120 (1970).

    Google Scholar 

  5. N. V. Bondarenko, Zh. Obshch. Khim.,37, 332 (1967).

    CAS  Google Scholar 

  6. S. M. Kupchan and C. I. Ayres, J. Pharm. Sci.,48, 440 (1959).

    Article  CAS  Google Scholar 

  7. W. Poethke, Die Alkaloide von Veratrum Album L., Habilitationsschrift, Leipzig,58, (1937).

  8. J. Fried, P. Numerof, and N. H. Goy, J. Amer. Chem. Soc.,74, 3041 (1952).

    Article  CAS  Google Scholar 

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Vitebsk Technological Institute of Light Industry. Translated from Khimiya Prirodnykh Soedinenii, No. 1, pp. 54–57, January–February, 1973.

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Bondarenko, N.V. The positions of the acyl groups in germerine and germitrine. Chem Nat Compd 9, 47–49 (1973). https://doi.org/10.1007/BF00580889

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  • DOI: https://doi.org/10.1007/BF00580889

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