Chemistry Letters p. 2015 - 2018 (1990)
Update date:2022-07-29
Topics: Enantiomer NMR spectroscopy Chiral Chromatography Stereoselective synthesis Optical rotation X-ray crystallography Absolute stereochemistry Diastereomer
Koreeda, Masato
Brown, Lindsey
Valdes, Leander J.
The absolute stereostructures of the hallucinogenic diterpenes salvinorin A and B have been unambiguously determined by the use of the non-empirical exciton chirality circular dichroism method on their 1α,2α-diol dibenzoate derivative.
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