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Modification and Functionalization of the Guanidine Group by Tailor-made Precursors
Published on: April 27, 2017
A simple chromatographic route for the isolation of meso diaminopimelic acid
Gábor K Tóth1, Anasztázia Hetényi, István Ilisz
1Department of Medical Chemistry, University of Szeged, Szeged, Hungary.
Abstract:
Meso diaminopimelic acid is an important noncoded amino acid found in Gram-negative bacterial peptidoglycan. In spite of its importance, this stereoisomer is not available commercially. A simple, economical procedure was developed for the isolation of pure meso diaminopimelic acid via an high-performance liquid chromatography separation. In our new approach, the underivatized three isomers of diaminopimelic acid were separated on a crown ether-based chiral stationary phase. For the structure identification, (1)H NMR spectroscopy was applied.

