Facile discrimination of aldose enantiomers by reversed-phase HPLC

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Abstract

One-pot reactions of aldoses with L-cysteine methyl ester and o-tolyl isothiocyanate yielded methyl 2-(polyhydroxyalkyl)-3-(o-tolylthiocarbamoyl)- thiazolidine-4(R)-carboxylates. Direct HPLC analysis of the reaction mixture and UV detection at 250 nm discriminated D- and L-enantiomers of aldoses. The reaction was applied to the determination of absolute configuration the sugar residues of an aroma precursor. © 2007 Pharmaceutical Society of Japan.

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Tanaka, T., Nakashima, T., Ueda, T., Tomii, K., & Kouno, I. (2007). Facile discrimination of aldose enantiomers by reversed-phase HPLC. Chemical and Pharmaceutical Bulletin, 55(6), 899–901. https://doi.org/10.1248/cpb.55.899

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