2001
DOI: 10.1002/1522-2683(200107)22:12<2616::aid-elps2616>3.0.co;2-g
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Enantioseparation of hydroxy acids on easy-to-prepare continuous beds for capillary electrochromatography

Abstract: 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.

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Cited by 58 publications
(15 citation statements)
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“…This CSP was applied to the chiral separation of underivatized amino acids [537] and hydroxy acids [538] using phosphate buffer pH 4.4/copper(II)sulfate as mobile phase . The same capillary was used for CEC, capillary LC and pressure supported CEC.…”
Section: Monolithic Cspsmentioning
confidence: 99%
“…This CSP was applied to the chiral separation of underivatized amino acids [537] and hydroxy acids [538] using phosphate buffer pH 4.4/copper(II)sulfate as mobile phase . The same capillary was used for CEC, capillary LC and pressure supported CEC.…”
Section: Monolithic Cspsmentioning
confidence: 99%
“…The applicability of this new approach to the chiral separation of underivatized AAs has been demonstrated. Additionally, this kind of solid phase in CEC easily prepared by in situ polymerization of monomers, including an L‐4‐hydroxyproline derivative showed chiral recognition ability for several hydroxy acids []. As a further study, by using diallyl‐dimethylammonium chloride (DADMAC) as a positive charge‐providing agent in CEC monolithic column, this phase was applied in the chiral separation of hydroxy monocarboxylic acids and hydroxy dicarboxylic acids, respectively [].…”
Section: Cle‐cecmentioning
confidence: 99%
“…Hjertén used a similar approach involving the copolymerization of methacrylamide, piperazine diacrylamide, and vinylsulfonic acid in the presence of a l-4-hydroxyproline derivative to afford monolithic CEC columns that could be used for ligand-exchange CEC of underivatized amino acids [102] or hydroxy acids [103]. Similar polymerizations in the presence of 2-hydroxy-3-allyloxy-propyl-␤-cyclodextrin led to monoliths that enabled enantiomeric resolution of acidic, neutral and basic drugs [104].…”
Section: Enantioselective Separationsmentioning
confidence: 99%