2015
DOI: 10.1007/s10337-015-2923-x
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Development of Electrophoretic Methods for Simultaneous Determination of Enantiomeric Ratio and Composition of Diastereomeric Salt Mixtures

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Cited by 8 publications
(12 citation statements)
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“…An overview of EKC‐UV methods applicable for quality control of pharmaceuticals published since 2015 is provided in Table 3 [71–106]. The most frequently, CDs were used as chiral selectors in these works, owning to their advantages, such as low cost, good stability, low UV cut‐off, high water solubility, and excellent chiral selectivity.…”
Section: Electrokinetic Chromatographymentioning
confidence: 99%
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“…An overview of EKC‐UV methods applicable for quality control of pharmaceuticals published since 2015 is provided in Table 3 [71–106]. The most frequently, CDs were used as chiral selectors in these works, owning to their advantages, such as low cost, good stability, low UV cut‐off, high water solubility, and excellent chiral selectivity.…”
Section: Electrokinetic Chromatographymentioning
confidence: 99%
“…Evaluation of extraction efficiency, conversion, and enantioselectivity achieved within the preparation of enantiopure ibuprofen in a resolvation experiment via diastereomeric salt formation was reported by Varga et al. [84]. The separation of ibuprofen enantiomers and resolving agent phenylethylamine was achieved using permethylated‐β‐CD as a chiral selector.…”
Section: Electrokinetic Chromatographymentioning
confidence: 99%
See 1 more Smart Citation
“…In a different study, Varga et al. developed a method for the simultaneous determination of enantiomeric ratio and composition of diastereomeric salt mixtures. Briefly, a modified Pope‐Peachy method with diastereomeric salt formation was performed in order to obtain enantiomerically pure compounds.…”
Section: Chiral Selectorsmentioning
confidence: 99%
“…Varga et al. demonstrated the feasibility of the approach using cis ‐permethrinic acid and ibuprofen as model compounds which were resolved via crystallization with R ‐1‐phenylethalamine . The analytical enantioseparation of the compounds was achieved in a fused‐silica capillary using a 50 mM Britton‐Robinson buffer with a pH between 7.0 and 7.2 depending on the analyte using 10 to 12.5 mM TM‐β‐CD as chiral selector.…”
Section: Separation and Analysis Of Small Moleculesmentioning
confidence: 99%