Abstract
The sesquiterpene lactone argolide has been converted into its 1(10)-epoxide. The structure of the latter has been investigated by NMR, x-ray structural analysis, and molecular mechanics.
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S. M. Adekenov, K. A. Aituganov, K. M. Turdybekov, S. V. Lindeman, and Yu. T. Struchkov, Khim. Prir. Soedin., 653 (1991).
F. H. Allen, O. Kennard, D. G. Watson, L. Brammer, A. G. Orpen, and R. Taylor, J. Chem. Soc., Perkin Trans. II, S1 (1987).
J. L. Breton, F. Camps, J. Coll, L. Eguren, J. A. Gavin, A. G. Gonzalez, X. Martorell, C. Miravitlles, E. Molins, and J. Torramilans, Tetrahedron,41, 3141 (1985).
H. Haasnoot, F. A. A. M. de Leeuw, and C. Altona, Tetrahedron,36, 2783 (1981).
H. Günther, NMR Spectroscopy: An Introduction, Wiley, New York (1980).
W. Z. Wang, R. X. Tan, Y. M. Yao, Q. Wang, and F. X. Jiang, Phytochemistry,37, No. 5, 1347 (1994).
A. T. Kulyyasov, T. S. Seitembetov, K. M. Turdybekov, and S. M. Adekenov, Khim. Prir. Soedin., 879 (1996).
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Translated from Khimiya Prirodnykh Soedinenii, No. 1, pp. 60–64, January–February, 1998.
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Turdybekov, K.M., Edil'baeva, T.T., Raldugin, V.A. et al. Molecular and crystal structures of argolide epoxide. Chem Nat Compd 34, 44–47 (1998). https://doi.org/10.1007/BF02249684
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DOI: https://doi.org/10.1007/BF02249684