Abstract
The configurational and conformational peculiarities of the cis and trans isomers of decahydroquinoline and decahydro-4-quinolone are discussed, and information on a new class of cis-decahydroquinoline alkaloid-neurotoxins and some data on the effect of the three-dimensional structures of decahydroquinoline derivatives on pharmacological activity are presented.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 5, pp. 579–599, May, 1987.
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Grishina, G.V., Potapov, V.M. Stereochemistry of decahydroquinoline and decahydro-4-quinolone (review). Chem Heterocycl Compd 23, 475–493 (1987). https://doi.org/10.1007/BF00476371
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DOI: https://doi.org/10.1007/BF00476371