PREPARATION AND EVALUATION OF THE CHIRAL STATIONARY PHASES BASED ON N-4-(2,5,6-TRICHLORO-1,3-DICYANO)-PHENYL DERIVATIVES OF L-α-AMINO ACIDS
Author:
Affiliation:
1. a Ruđer Bošković Institute , P.O. Box 1016, Bijenička cesta 54, Zagreb, Croatia, 10000
2. b Ruđer Bošković Institute , P.O. Box 1016, Bijenička cesta 54, Zagreb, Croatia, 10000
Publisher
Informa UK Limited
Subject
Clinical Biochemistry,Pharmaceutical Science,Biochemistry,Analytical Chemistry
Link
https://www.tandfonline.com/doi/pdf/10.1081/JLC-100100409
Reference19 articles.
1. Direct separation of carboxylic acid enantiomers by high-performance liquid chromatography with amide and urea derivatives bonded to silica gel as chiral stationary phases
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3. Comparison between silica-bonded chiral stationary phases derived from 3,5-disubstituted N-benzoyl-(S)-phenylalanine and (S)-cyclohexylalanine in the resolution of racemic compounds by liquid chromatography
4. An Improved (S)-Leucine-Derived π-Acidic HPLC Chiral Stationary Phase for the Resolution of π-Acidic Racemates
5. A Chiral Recognition Mechanism Proposed for Resolving π‐Acidic Racemates on π‐Acidic Chiral Stationary Phases Derived from ( S )‐Leucine
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