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3,5-dimethylphenylcarbamate

National Institutes of Health

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Phenylcarbamates

Papers overview

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2014
2014
Enantioseparation of pyroglutamide derivatives on polysaccharide based chiral stationary phases by high-performance liquid chromatography and supercritical fluid chromatography: a comparative study.
2008
2008
Polyproline derivatives as chiral selectors in high performance liquid chromatography: chromatographic and conformational studies.
2007
2007
Enantioseparation of 1-phenyl-1-propanol on cellulose-derived chiral stationary phase by supercritical fluid chromatography II. Non-linear isotherm.
2007
2007
Titanized or Zirconized Porous Silica Modified with a Cellulose Derivative as New Chiral Stationary Phases
Spherical porous silica supports modified with titanium or zirconium alkoxides were prepared, and allyl groupswere chemically… 
2007
2007
Preparation and chiral recognition ability of crosslinked beads of polysaccharide derivatives.
The spherical beads consisting of cellulose 3,5-dimethylphenylcarbamate with partial hydroxyl groups were prepared to be used as… 
Highly Cited
2005
Highly Cited
2005
Solvent versatility of immobilized 3,5-dimethylphenylcarbamate of amylose in enantiomeric separations by HPLC.
2004
2004
Preparation of a positively charged cellulose derivative chiral stationary phase with copolymerization reaction for capillary electrochromatographic separation of enantiomers
A positively charged chiral stationary phase (CSP) was prepared by chemically immobilizing cellulose 3,5‐dimethylphenylcarbamate… 
Highly Cited
2003
Highly Cited
2003
Preparation of chiral stationary phase for HPLC based on immobilization of cellulose 3,5-dimethylphenylcarbamate derivatives on silica gel.
The immobilization of cellulose 3,5-dimethylphenylcarbamate derivatives having a polymerizable vinyl group, i.e., 4… 
1997
1997
Enantioselective determination of oxprenolol in human plasma using dialysis coupled on-line to reversed-phase chiral liquid chromatography.
1994
1994
Direct enantioselective separation of bevantolol by high-performance liquid chromatography on normal and reverse cellulose chiral stationary phases.
A direct, isocratic and simple chromatographic method is described for the enantiomeric separation of bevantolol (BEV) using… 
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