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NMR and HPLC study of chiral selectors with naphthyl unit

Doubling of resonances in NMR spectra of chiral selectors with naphthyl group attached to the tertiary amide nitrogen atom has been noticed what revealed the presence of two isomers. To test the enantiorecognition ability of these chiral selectors they are covalently bonded to the HPLC silica gel. Those kind of chiral stationary phases were compared with analogous commercial leucine chiral stationary phase. They exhibit the better enantioseparation results what indicate that the existence of cis/trans isomers doesn’ t have the negative influence on their enantioselective ability.

peaks doubling ; dynamical NMR ; peak coalescence ; chiral HPLC

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