Summary
For all the bisbenzyltetrahydroisoquinoline alkaloids considered except thalisopine, positive CEs are found in the case of the SS configuration and negative CEs in the case of the RS configuration.
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Literature cited
A. R. Battersby et al., J. Chem. Soc., 2239, 1965.
J. C. Craig et al., Tetrah.,22, 1335, 1966.
S. Kh. Maekh, Z. F. Ismailov, and S. Yu. Yunusov, KhPS [Chemistry of Natural Compounds],4, 393, 1968.
S. Kh. Maekh and S. Yu. Yunusov, KhPS [Chemistry of Natural Compounds],1, 188, 1965.
M. Shamma et al., Chem. Comm., 7, 1966.
Kh. G. Pulatova, S. Kh. Maekh, Z. F. Ismailov, and S. Yu. Yunusov, KhPS [Chemistry of Natural Compounds],4, 394, 1968.
J. Boldas et al., Tetrah. Let., 6315, 1968.
M. V. Telezhenetskaya, Z. F. Ismailov, and S. Yu. Yunusov, KhPS [Chemistry of Natural Compounds],2, 107, 1966.
T. Tomimatsu, RZhKhim., 9zh291, 1961.
M. R. Falco et al., Tetrah. Let., 1953, 1968.
S. M. Kupchan et al., J. Am. Chem. Soc.,89, 3075, 1967.
C. Djerassi, K. Mislow, and M. Shamma, Exper.,18, 53, 1962.
Z. F. Ismailov and S. Yu. Yunusov, KhPS [Chemistry of Natural Compounds],2, 43, 1966.
Kh. S. Umarov, Z. F. Ismailov, and S. Yu. Yunusov, KhPS [Chemistry of Natural Compounds],6, 444, 1970.
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Institute of the Chemistry of Plant Substances, Academy of Sciences of the Uzbek SSR. Translated from Khimiya Prirodnykh Soedinenii, No. 6, pp. 705–708, November–December, 1970.
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Moiseeva, G.P., Ismailov, Z.F. & Yunusov, S.Y. Optical rotatory dispersion of some thalictrum alkaloids. Chem Nat Compd 6, 715–717 (1970). https://doi.org/10.1007/BF00565340
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DOI: https://doi.org/10.1007/BF00565340