Chiral recognition ability and solvent versatility of bonded amylose tris(3,5-dimethylphenylcarbamate) chiral stationary phase: Enantioselective liquid chromatographic resolution of racemic N-alkylated barbiturates and thalidomide analogs
Author:
Publisher
Wiley
Subject
Organic Chemistry,Spectroscopy,Drug Discovery,Pharmacology,Catalysis,Analytical Chemistry
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1. Barbitursäurederivate, 30. Mitt. Synthese racem. und optisch aktiver basisch substituierter Barbitursäuren
2. Synthese der Racemate und der Enantiomere von 3-Alkylthalidomidanaloga und Bestimmung ihrer absoluten Konfiguration
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5. Analytical and semipreparative high performance liquid chromatography enantioseparation of new substituted 1-thiocarbamoyl-3,5-diaryl-4,5-dihydro-(1H)-pyrazoles on polysaccharide-based chiral stationary phases in normal-phase, polar organic and reversed-phase conditions
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1. Enantioselective separation of racemates using CHIRALPAK IG amylose-based chiral stationary phase under normal standard, non-standard and reversed phase high performance liquid chromatography;Journal of Chromatography A;2018-01
2. Study of enantioselectivity on an immobilized amylose carbamate stationary phase under subcritical fluid chromatography;Journal of Separation Science;2013-11-18
3. Enantioseparation Properties of the Biselector Chiral Stationary Phase Derived from Amylose Tris(phenylcarbamate) and Amylose Tris(benzoate);Current Analytical Chemistry;2013-01-01
4. Complementary enantiorecognition patterns and specific method optimization aspects on immobilized polysaccharide-derived chiral stationary phases;Journal of Chromatography A;2012-12
5. Allyl m-Trifluoromethyldiazirine Mephobarbital: An Unusually Potent Enantioselective and Photoreactive Barbiturate General Anesthetic;Journal of Medicinal Chemistry;2012-07-17
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