Comparison, applications, advantages, and limitations of immobilized and coated amylose tris-(3,5-dimethylphenylcarbamate) chiral stationary phases in HPLC

Journal of Liquid Chromatography and Related Technologies

Volumn 28, Issue 18, 2005, Pages 2863-2874

  Ghanem, Ashraf ^a   Aboul Enein, Hassan Y ^a  

^a KING FAISAL SPECIALIST HOSPITAL AND RESEARCH CENTER   (Saudi Arabia)

Author keywords

Acidic drugs; Amylose tris (3,5 dimethylphenylcarbamate); Chiralpak AD; Chiralpak IA; Enantioseparation; HPLC; Kinetic resolution

Indexed keywords

CHELATION; DISSOLUTION; DRUG PRODUCTS; POLYSACCHARIDES; REACTION KINETICS; SEPARATION;

ACIDIC DRUGS; CHIRALPAK IA; KINETIC RESOLUTION;

HIGH PERFORMANCE LIQUID CHROMATOGRAPHY;

2 METHOXYMANDELIC ACID; 2 PHENOXYPROPIONIC ACID; 2 PROPANOL; ACETIC ACID ETHYL ESTER; AMYLOSE; AMYLOSE TRIS(3,5 DIMETHYLPHENYLCARBAMATE); BUTANOL; CARBAMIC ACID DERIVATIVE; CARPROFEN; DICHLOROMETHANE; FENOPROFEN; FLURBIPROFEN; HEXANE; IBUPROFEN; KETOPROFEN; MANDELIC ACID DERIVATIVE; NAPROXEN; NOVOZYM 435; ORGANIC SOLVENT; PIKETOPROFEN; PIRPROFEN; PROPIONIC ACID DERIVATIVE; ROSMARINIC ACID; SILICON DIOXIDE; TETRAHYDROFURAN; TRIACYLGLYCEROL LIPASE; UNCLASSIFIED DRUG; WARFARIN;

ARTICLE; CHEMICAL MODIFICATION; CHIRAL CHROMATOGRAPHY; CHIRALITY; ELUTION; ENANTIOMER; ENANTIOSELECTIVITY; ESTERIFICATION; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; IMMOBILIZATION; PURIFICATION; RACEMIC MIXTURE; REACTION ANALYSIS; SEPARATION TECHNIQUE;

EID: 27744464838     PISSN: 10826076     EISSN: 1520572X     Source Type: Journal    
DOI: 10.1080/10826070500269919     Document Type: Article

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