Reversed-phase liquid chromatographic resolution of underivatized d,l-amino acids using chiral eluents
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,General Medicine,Biochemistry,Analytical Chemistry
Reference14 articles.
1. Separation of Optical Isomers as Diastereomeric Derivatives by High Performance Liquid Chromatography
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3. Reversed-phase high-performance liquid chromatographic resolution of non-esterified enantiomeric amino acids by derivatization with 2,3,4,6-tetra-o-acetyl-β-d-glucopyranosyl isothiocyanate and 2,3,4-tri-o-acetyl-α-d-arabinopyranosyl isothiocyanate
4. Separation of D and L Amino Acids by Liquid Chromatography: Use of Chiral Eluants
5. Ligand chromatography as a novel method for the investigation of mixed complexes: stereoselective effects in α-amino acid copper(II) complexes
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1. Enantiomeric Separation by the Chiral Mobile Phase Additives;Chiral Separations By Liquid Chromatography And Related Technologies;2003-06-03
2. l and d-cysteine derivatives of β-cyclodextrim: different molecular recognition properties of their copper(II) complexes for amino acids;Inorganica Chimica Acta;1998-07
3. Highly Effective Separation and Highly Sensitive Detection for Clinical Chemistry and Biochemistry;YAKUGAKU ZASSHI;1998
4. Optical resolution of new quinolone drugs by capillary electrophoresis with ligand-exchange and host-guest interactions;Journal of Chromatography A;1997-01
5. HPLC Determination of Enantiomeric Purity of Protected Amino Acid Derivatives Used in Peptide Synthesis;Journal of Liquid Chromatography;1994-08
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