Journal of High Resolution Chromatography · 1990 · 46 citations · 8 references
PharmacyBiochemistryChemistryCarbohydrate BiochemistryCarbohydrate ChemistryPolymer ChemistryCarbohydrate StructureCellulose BiochemistryCellulose ChemistryPolysaccharide PropertiesPolysaccharide StructureStarch ChemistryPolysaccharide MaterialsPolysaccharide-based Chiral Stationary Phases
Abstract Twenty different tris(phenylcarbamate)s of cellulose were synthesized and evaluated as chiral stationary phases for HPLC. Optical resolving power of the tris(phenylcarbamate)s depends on the substituents introduced on the phenyl groups. Optical resolving abilities of amylose tris(phenylcarbamate)s were also evaluated. In most cases, either cellulose tris(3,5‐dimethylphenylcarbamate) or amylose tris(3,5‐dimethylphenylcarbamate) exhibited the highest optical resolving ability. Aralkylcarba‐mates such as benzyl‐ and 1‐phenylethylcarbamates of cellulose and amylose were also tested as chiral stationary phases. ( S )‐1‐Phenylethylcarbamate of amylose showed a high optical resolving power.
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Yoshio Okamoto, Mitsunobu Kawashima, Koichi Hatada · Journal of Chromatography A · 1986 · 669 citations
Yoshio Okamoto, Mitsunobu Kawashima, Koichi Hatada · Journal of the American Chemical Society · 1984 · 483 citations
Pharmacy, Biochemistry, Chemistry +17
Chromatographic chiral resolution
Yoshio Okamoto, Ryo Aburatani, Koichi Hatada · Journal of Chromatography A · 1987 · 201 citations
Resolution of enantiomers by HPLC on cellulose derivatives
Akito Ichida, T. Shibata, Ichiro Okamoto et al. · Chromatographia · 1984 · 197 citations