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Volumn 950, Issue 1-2, 2002, Pages 65-74
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Synthesis and chromatographic properties of a novel chiral stationary phase derived from heptakis(6-azido-6-deoxy-2,3-di-O-phenylcarbamoylated)-β-cyclodextrin immobilized onto amino-functionalized silica gel via multiple urea linkages
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Author keywords
Chiral stationary phases, LC; Enantiomer separation
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Indexed keywords
AMINES;
CHROMATOGRAPHIC ANALYSIS;
DRUG PRODUCTS;
METHANOL;
PH EFFECTS;
SILICA GEL;
UREA;
ENANTIOMERS;
AMINO ACIDS;
ACETIC ACID DERIVATIVE;
AMINE;
ATROPINE;
BETA ADRENERGIC RECEPTOR BLOCKING AGENT;
BETA CYCLODEXTRIN;
BUFFER;
HEPTAKIS(6 AZIDO 6 DEOXY 2,3 DI O PHENYLCARBAMOYL) BETA CYCLODEXTRIN;
ISOPRENALINE;
METHANOL;
SILICA GEL;
TRIETHYLAMMONIUM ACETATE;
UNCLASSIFIED DRUG;
UREA;
ARTICLE;
CHEMICAL ANALYSIS;
CHEMICAL REACTION;
CHIRAL CHROMATOGRAPHY;
CHIRALITY;
ENANTIOMER;
IMMOBILIZATION;
PH;
PRIORITY JOURNAL;
STAUDINGER REACTION;
STRUCTURE ANALYSIS;
BETA-CYCLODEXTRINS;
CHROMATOGRAPHY, HIGH PRESSURE LIQUID;
CYCLODEXTRINS;
HYDROGEN-ION CONCENTRATION;
SILICON DIOXIDE;
SPECTROSCOPY, FOURIER TRANSFORM INFRARED;
STEREOISOMERISM;
UREA;
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EID: 0037087113
PISSN: 00219673
EISSN: None
Source Type: Journal
DOI: 10.1016/S0021-9673(02)00043-2 Document Type: Article |
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Times cited : (65)
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References (29)
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