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Fast chiral separation by ligand-exchange HPLC using a dynamically coated monolithic column.

Martin G Schmid·Karin Schreiner·Daniela Reisinger·Gerald Gübitz
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Abstract

The preparation and application of dynamically coated ligand-exchange chromatography phases for enantioseparation is described. The phases were prepared by pumping a solution of N-decyl-L-4-hydroxyproline, N-hexadecyl-L-4-hydroxyproline, or N-2-hydroxydodecyl-L-4-hydroxyproline through a commercially available monolithic RP-18 column. These coatings are stable against desorption for months at ambient temperature when aqueous mobile phases are used. The columns were applied to the chiral separation of amino acids, glycyl dipeptides and diastereomeric dipeptides, and tripeptides. The chiral selector can be removed or changed easily by washing the column with ACN or methanol. Ultrafast separations in the range of seconds were achieved using high flow rates.

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Amino AcidsChromatography, LiquidHydroxyprolineLigandsMaterials TestingMolecular StructurePeptidesStereoisomerismJournal Article

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Martin G Schmid, Karin Schreiner, Daniela Reisinger, Gerald Gübitz. 2006. Fast chiral separation by ligand-exchange HPLC using a dynamically coated monolithic column.. https://doi.org/10.1002/jssc.200600102

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