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Enantioseparation of hydroxy acids on easy‐to‐prepare continuous beds for capillary electrochromatography
Author(s) -
Schmid Martin G.,
Grobuschek Nina,
Lecnik Oliver,
Gübitz Gerald,
Végvári Ákos,
Hjertén Stellan
Publication year - 2001
Publication title -
electrophoresis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.666
H-Index - 158
eISSN - 1522-2683
pISSN - 0173-0835
DOI - 10.1002/1522-2683(200107)22:12<2616::aid-elps2616>3.0.co;2-g
Subject(s) - capillary electrochromatography , electrochromatography , chemistry , amino acid , monomer , hydroxyproline , capillary electrophoresis , chromatography , polymerization , combinatorial chemistry , chiral stationary phase , organic chemistry , high performance liquid chromatography , polymer , biochemistry
This paper deals with the enantioseparation of hydroxy acids by ligand‐exchange capillary electrochromatography. A chiral continuous bed was easily prepared by in situ polymerization of monomers, including an L ‐4‐hydroxyproline derivative. This phase showed chiral recognition for several hydroxy acids, in addition to amino acids.