Chloromethylphenylcarbamate derivatives of cellulose as chiral stationary phases for high-performance liquid chromatography

1994/06/01 by Bezhan Chankvetadze, Eiji Yashima, Yoshio Okamoto · 8 citations
Chemistry · Engineering · #Analytical Chemistry and Chromatography #Microfluidic and Capillary Electrophoresis Applications #Mass Spectrometry Techniques and Applications

paper · doi:10.1016/0021-9673(94)80278-5

Citations

• Chromatographic resolution

Cited by

• Recent developments on polysaccharide-based chiral stationary phases for liquid-phase separation of enantiomers
• 3-Fluoro-, 3-chloro- and 3-bromo-5-methylphenylcarbamates of cellulose and amylose as chiral stationary phases for high-performance liquid chromatographic enantioseparation
• Synthesis of cellulose carbamates bearing regioselective substituents at 2,3- and 6-positions for efficient chromatographic enantioseparation
• Predicting enantioseparations on polysaccharide-based stationary phases using achiral and chiral molecular descriptors
• Preparation of cellulose derivative bearing bulky 4‐(2‐benzothienyl)phenylcarbamate substituents as chiral stationary phase for enantioseparation
• Chiral Nano-Liquid Chromatography and Dispersive Liquid-Liquid Microextraction Applied to the Analysis of Antifungal Drugs in Milk. [europepmc]
• Characteristic and complementary chiral recognition ability of four recently developed immobilized chiral stationary phases based on amylose and cellulose phenyl carbamates and benzoates. [europepmc]
• Chiral Hydroxy Metabolite of Mebendazole: Analytical and Semi-Preparative High-Performance Liquid Chromatography Resolution and Chiroptical Properties. [europepmc]