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Structure and configuration of severtzidine

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Summary

1. From the combined alkaloids of the epigeal part ofKorolkowia sewertsovii Rgl. collected at Saryagach we have isolated sevkorine, korseveriline, korseveridine, korseverinine, a base with mp 212–214°C, and the new alkaloid severtizidine.

2. On the basis of a study of the chemical and physical characteristics of the alkaloids itself and the products of its transformations, the most probable structure and configuration of severtzidine has been established as 3β,6β,14α-trihydroxycevanine.

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Literature cited

  1. S. Yu. Yunusov, R. A. Konovalova, and A. P. Orekhov, Zh. Obshch. Khim., 1911 (1939).

  2. G. Kittél and A. S. Sadykov, Dokl. Akad. Nauk UzSSR, 11 (1948).

  3. R. N. Nuriddinov and S. Yu. Yunusov, Dokl. Akad. Nauk UzSSR, 47 (1962).

  4. R. N. Nuriddinov and S. Yu. Yunusov, Khim. Prirodn. Soedin., 60 (1968).

  5. R. N. Nuriddinov and S. Yu. Yunusov, Khim. Prirodn. Soedin., 101 (1968); 258 (1968); 767 (1971).

    Google Scholar 

  6. R. N. Nuriddinov and S. Yu. Yunusov, Khim. Prirodn. Soedin., 773 (1971).

  7. R. N. Nuriddinov, R. Shakirov, and S. Yu. Yunusov, Khim. Prirodn. Soedin., 316 (1967).

  8. H. Budzikiewicz, Tetrahedron,20, 2264 (1964).

    Google Scholar 

  9. IUPAC-IUB Revised Tentative Rules for the Nomenclature of Steroids, J. Org. Chem.,34, 1517 (1969).

    Article  Google Scholar 

  10. F. Bohlman, Ber.,91, 2157 (1958).

    Google Scholar 

  11. T. M. Moynehan, K. Schofield, R. A. V. Jones, and A. R. Katritzky, J. Chem. Soc., 2637 (1962).

  12. H. Mohrle, C. Karl, and U. Schedegger, Tetrahedron,24, 6813 (1968).

    Article  Google Scholar 

  13. S. Ito, J. B. Stothers, and S. M. Kupchan, Tetrahedron,20, 913 (1964).

    Article  CAS  Google Scholar 

  14. F. Bohlmann, D. Schumann, and C. Arndt, Tetrahedron Lett.,31, 2705 (1965).

    Article  Google Scholar 

  15. R. N. Nuriddinov, A. I. Saidkhodzhaev, M. R. Yagudaev, and S. Yu. Yunusov, Khim. Prirodn. Soedin., 333 (1968).

  16. R. F. Zürcher, Helv. Chim. Acta,46, 2054 (1963).

    Article  Google Scholar 

  17. R. N. Nuriddinov, A. I. Saidkhodzhaev, and S. Yu. Yunusov, Khim. Prirodn. Soedin., 61 (1969).

  18. I. Fried, P. Grabowich, E. F. Sabo, and A. I. Cohen, Tetrahedron,20, 2297 (1964).

    Article  CAS  Google Scholar 

  19. M. L. Mihailovic, L. Lorens, M. Rogic, A. Melera, and M. Stefanovic, Tetrahedron,22, 2345 (1966).

    Article  CAS  Google Scholar 

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Authors
  1. K. Samikov
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  2. R. Shakitov
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  3. S. Yu. Yunusov
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Additional information

Institute of the Chemistry of Plant Substances, Academy of Sciences of the Uzbek SSR, Tashkent. Translated from Khimiya Prirodnykh Soedinenii, No. 3, pp. 367–371, May–June, 1976.

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Samikov, K., Shakitov, R. & Yunusov, S.Y. Structure and configuration of severtzidine. Chem Nat Compd 12, 320–323 (1976). https://doi.org/10.1007/BF00567807

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