Summary
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1.
The structure of 2′,3′,4′,1″,2″,3″-hexamethoxy-6,7-dimethyl-1,2: 3,4-dibenzo-1,3-cyclooctadien-6-ol is proposed for schizandrin.
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2.
It is suggested thatγ-schizandrin has the same carbon skeleton.
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3.
A probably biogenetic scheme for the formation of compounds of this type is given.
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N. K. Kochetkov, A. Ya. Khorlin, and O. S. Chizhov, Zh. obshch. khimii,31, 3454 (1961).
N. K. Kochetkov, A. Y. Khorlin, O. S. Chizhov, and V. I. Sheichenko, Tetrahedron Letters, 1961, No. 20, 730.
J. L. Hartwell, A. W. Schrecker, and G. Y. Greenberg, J. Amer. Chem. Soc.,74, 6285 (1952).
W. Meyer, Z. analyt. Chem.,141, 345 (1954).
D. E. Hathway, J. Chem. Soc., 1957, 519.
O. T. Schmidt and K. Demmler, Liebigs Ann. Chem.,576, 85 (1952).
N. K. Kochetkov, A. Ya. Khorlin, and O. S. Chizhov, Izv. AN SSSR, Otd. khim. n., 1962, 856.
G. H. Beaven, D. M. Hall, M. S. Lesslie, and E. E. Turner, J. Chem. Soc., 1952, 854; G. H. Beaven, D. M. Hall, M. S. Lesslie, E. E. Turner, and G. R. Bird, J. Chem. Soc., 1954, 131; G. H. Beaven, G. R. Bird, D. M. Hall, E. A. Johnson, J. E. Ladbury, M. S. Lesslie, and E. E. Turner, J. Chem. Soc., 1955, 2708.
J. N. Shoolery and M. T. Rogers, J. Amer. Chem. Soc.,80, 5121 (1958).
J. Polonsky and A. Gaudemer, Bull. Soc. chim. France, 1961, 1432.
N. F. Chamberlain, Uspekhi khimii,28, 1353 (1959).
R. D. Haworth, J. Chem. Soc., 1942, 448.
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Kochetkov, N.K., Khorlin, A.Y., Chizhov, O.S. et al. Chemical investigation of Schizandra chinensis. Russ Chem Bull 11, 792–796 (1962). https://doi.org/10.1007/BF00905305
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DOI: https://doi.org/10.1007/BF00905305