Chromatographic resolution

1986/01/01 by Yoshio Okamoto, Mitsunobu Kawashima, Koichi Hatada · 21 citations
Chemistry · Engineering · #Analytical Chemistry and Chromatography #Microfluidic and Capillary Electrophoresis Applications #Mass Spectrometry Techniques and Applications

paper · doi:10.1016/s0021-9673(01)83736-5

Citations

• High-pressure liquid chromatography on triacetylcellulose

Cited by

• Recent developments on polysaccharide-based chiral stationary phases for liquid-phase separation of enantiomers
• Chloromethylphenylcarbamate derivatives of cellulose as chiral stationary phases for high-performance liquid chromatography
• Fabrication of cellulose derivative coated spherical covalent organic frameworks as chiral stationary phases for high-performance liquid chromatographic enantioseparation
• Resolution by high-performance liquid chromatography using polysaccharide carbamates and benzoates as chiral stationary phases
• Synthesis and application of immobilized polysaccharide-based chiral stationary phases for enantioseparation by 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
• Synthesis of cellulose carbamates bearing regioselective substituents at 2,3- and 6-positions for efficient chromatographic enantioseparation
• Influence of vinyl monomers and temperature on immobilization of cellulose 3,5-dimethylphenylcarbamate onto silica gel as chiral stationary phases for high-performance liquid chromatography
• 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 covalent organic cages: Construction and chiral functions
• Synthesis of Optically Active Poly(diphenylacetylene)s Using Polymer Reactions and an Evaluation of Their Chiral Recognition Abilities as Chiral Stationary Phases for HPLC. [europepmc]
• Enantioseparation Using Cellulose Tris(3,5-dimethylphenylcarbamate) as Chiral Stationary Phase for HPLC: Influence of Molecular Weight of Cellulose. [europepmc]
• Temperature-Triggered Switchable Helix-Helix Inversion of Poly(phenylacetylene) Bearing l-Valine Ethyl Ester Pendants and Its Chiral Recognition Ability. [europepmc]
• Photochemically Immobilized 4-Methylbenzoyl Cellulose as a Powerful Chiral Stationary Phase for Enantioselective Chromatography. [europepmc]
• Chiral Stationary Phases for Liquid Chromatography: Recent Developments. [europepmc]
• Enantiomeric Recognition and Separation by Chiral Nanoparticles. [europepmc]
• Nonideal behavior of void volume markers in polar-organic chiral HPLC on polysaccharide-based chiral stationary phases. [europepmc]
• Optically active distorted cyclic triptycenes: chiral stationary phases for HPLC. [europepmc]
• Stereoselective Processes Based on σ-Hole Interactions. [europepmc]
• New Levan-Based Chiral Stationary Phases: Synthesis and Comparative HPLC Enantioseparation of (±)- trans -β-Lactam Ureas in the Polar Organic Mode. [europepmc]