Abstract
Three chiral derivatization reagents: 2-[4-(L-leucyl)aminophenyl]-6-methoxybenzoxazole, 2-[4-(D-phenylglycyl)amino-phenyl]-6-methoxybenzoxazole, and 2-[4-(L-phenylalanyl)aminophenyl]-6-methoxybenzoxazole, have been synthesized to permit separation of carboxylic acid enantiomers by high-performance liquid chromatography. Enantiomeric carboxylic acids were readily condensed with the chiral reagents in the presence of 2, 2′-dipyridyl disulfide and triphenylphosphine. The diastereometric amides formed were separated on a normal-phase column, and were sensitively detected fluorometrically at 375nm, with excitation at 330nm. The detection limit of L-PheBOX derivative of 2-phenylpropionic acid was 70fmol at a signal-to-noise ratio of 3.
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