A chiral stationary phase which affords unusually high levels of enantioselectivity
Author:
Publisher
Wiley
Subject
Organic Chemistry,Spectroscopy,Drug Discovery,Pharmacology,Catalysis,Analytical Chemistry
Reference7 articles.
1. Useful and easily prepared chiral stationary phases for the direct chromatographic separation of the enantiomers of a variety of derivatized amines, amino acids, alcohols, and related compounds
2. A Convenient Void Volume Marker for Several Chiral HPLC Columns
3. A new, easily accessible reciprocal chiral stationary phase for the chromatographic separation of enantiomers
4. Intermolecular proton[proton] nuclear Overhauser effects in diastereomeric complexes: support for a chromatographically derived chiral recognition model
5. X-ray crystallographic support of a chiral recognition model
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2. A chromatographic and computational study on the driving force operating in the exceptionally large enantioseparation of N-thiocarbamoyl-3-(4′-biphenyl)-5-phenyl-4,5-dihydro-(1H) pyrazole on a 4-methylbenzoate cellulose-based chiral stationary phase;Journal of Chromatography A;2014-01
3. Small Molecules as Chromatographic Tools for HPLC Enantiomeric Resolution: Pirkle-Type Chiral Stationary Phases Evolution;Chromatographia;2013-05-09
4. Separation of the Enantiomers of β-Blockers Using Brush Type Chiral Stationary Phase Derived from Conformationally Rigid α-Amino β-Lactam;Bulletin of the Korean Chemical Society;2010-03-20
5. A (4R)-Hydroxy-L-proline-derived chiral scaffold and its oligomers as chiral selectors in liquid chromatography chiral stationary phases for enantioseparation;Journal of Separation Science;2006-04
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