Synthesis of cellulose carbamates bearing regioselective substituents at 2,3- and 6-positions for efficient chromatographic enantioseparation

2018/08/18 by Jun Shen, Fan Wang, Wanying Bi +3 · 3 citations
Chemistry · Engineering · #Analytical Chemistry and Chromatography #Microfluidic and Capillary Electrophoresis Applications #Mass Spectrometry Techniques and Applications

paper · doi:10.1016/j.chroma.2018.08.032

Citations

• Chromatographic resolution
• High-pressure liquid chromatography on triacetylcellulose
• Chloromethylphenylcarbamate derivatives of cellulose as chiral stationary phases for high-performance liquid chromatography
• 3-Fluoro-, 3-chloro- and 3-bromo-5-methylphenylcarbamates of cellulose and amylose as chiral stationary phases for high-performance liquid chromatographic enantioseparation
• Recent developments on polysaccharide-based chiral stationary phases for liquid-phase separation of enantiomers
• Synthesis and application of immobilized polysaccharide-based chiral stationary phases for enantioseparation by high-performance liquid chromatography

Cited by

• Chiral Stationary Phases for Liquid Chromatography: Recent Developments. [europepmc]
• Progress in the Enantioseparation of β-Blockers by Chromatographic Methods. [europepmc]
• Synthesis of Polyanionic Cellulose Carbamates by Homogeneous Aminolysis in an Ionic Liquid/DMF Medium. [europepmc]