Resolution of chiral cannabinoids on amylose tris(3,5-dimethylphenylcarbamate) chiral stationary phase: effects of structural features and mobile phase additives.

Abstract

The separation of six pairs of chiral cannabinoids was achieved using a dimethylphenylcarbamate derivative of amylose, immobilized on silica gel (ChiralPak AD, Daicel), using 2-propanol and ethanol as the modifiers of n-hexane in the mobile phase. Good separation was achieved for most of the solutes in both solvent systems under various conditions. The… (More)

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Cite this paper

@article{Levin1993ResolutionOC, title={Resolution of chiral cannabinoids on amylose tris(3,5-dimethylphenylcarbamate) chiral stationary phase: effects of structural features and mobile phase additives.}, author={S. Levin and Saleh Abu-Lafi and Jan Zah{\'a}lka and Raphael Mechoulam}, journal={Journal of chromatography. A}, year={1993}, volume={654 1}, pages={53-64} }