Fast enantioseparation of arylglycine amides by capillary electrophoresis with highly sulfated-β-cyclodextrin as a chiral selector
- 1 May 2003
- journal article
- Published by Elsevier in Journal of Chromatography A
- Vol. 998 (1-2) , 221-228
- https://doi.org/10.1016/s0021-9673(03)00653-8
Abstract
No abstract availableKeywords
This publication has 31 references indexed in Scilit:
- Highly efficient and enantioselective synthesis of l-arylglycines and d-arylglycine amides from biotransformations of nitrilesTetrahedron Letters, 2001
- Enantioseparations in capillary electromigration techniques: recent developments and future trendsJournal of Chromatography A, 2001
- Chiral Separations in Capillary ElectrophoresisChemical Reviews, 2000
- Enantiomer separation of drugs by capillary electromigration techniquesJournal of Chromatography A, 2000
- Enantioselective determination by capillary electrophoresis with cyclodextrins as chiral selectorsJournal of Chromatography A, 2000
- High-performance liquid chromatographic separation of the enantiomers of unusual α-amino acid analoguesJournal of Chromatography A, 2000
- Recent innovations in enantiomer separation by electrochromatography utilizing modified cyclodextrins as stationary phasesElectrophoresis, 1999
- Dynamic kinetic resolution of phenylglycine esters via lipase-catalysed ammonolysisTetrahedron: Asymmetry, 1999
- Liquid chromatographic resolution of racemic amino acids and their derivatives on a new chiral stationary phase based on crown etherJournal of Chromatography A, 1998
- About some aspects of the use of charged cyclodextrins for capillary electrophoresis enantioseparationElectrophoresis, 1994