Fluorescence chiral derivatization reagents for high performance liquid chromatographic resolution of enantiomeric hydroxyl compounds.

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Abstract
Two sensitive and moderately reactive chiral derivatization reagents having a binaphthalene moiety as a fluorophore and carbonyl cyanide as a reacting group toward enantiomeric alcohols have been developed. The derivatization reagents, (-)- and (+)-2-methyl-1, 1′-binaphthalene-2′-carbonyl cyanides, were prepared from dimethyl-1, 1′-binaphthalene-2, 2′-dicarboxylate in several steps. Enantiomeric alcohols underwent facile derivatization with these reagents under mild condition. The diastereomeric esters formed from enantiomeric β-hydroxy acids and β-blockers were efficiently resolved by high performance liquid chromatography on a normal phase column. The resulting esters were highly responsive to a fluorescence detector (excitation wavelength 342nm; emission wavelength 420nm), the limit of detection being 200pg.

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