Abstract
(+)-Poly(triphenylmethyl methacrylate)-coated silica gel [Chiralpack OT(+)] was used for the separation of enantiomers of racemic isoflavanone, homoisoflavanone, isoflavan and 2-benzyltetralone derivatives. All the enantiomers of the above-mentioned compounds were separable. The efficiency of the separation depended on both the skeleton and substitution pattern of the racemic compounds. A relation between the number and polarity of substituents in the aromatic rings and the resolution and separation factors was observed.
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