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Volumn 923, Issue 1-2, 2001, Pages 27-36
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Conformational and temperature effects on separation of stereoisomers of a C3,C4-substituted β-lactamic cholesterol absorption inhibitor on amylose-based chiral stationary phases
a
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Author keywords
Lactams; Chiral stationary phases, LC; Conformational effects; Enantiomer separation; Temperature effects
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Indexed keywords
ADSORPTION;
DERIVATIVES;
LIQUID CHROMATOGRAPHY;
PHASE COMPOSITION;
SEPARATION;
THERMAL EFFECTS;
MOLECULAR FLEXIBILITY;
ISOMERS;
1,4 BIS(4 METHOXYPHENYL) 3 (3 PHENYLPROPYL) 2 AZETIDINONE;
AMYLOSE;
ANTILIPEMIC AGENT;
SCH 48462;
SCH 48678;
SCH 48679;
UNCLASSIFIED DRUG;
ARTICLE;
CHIRALITY;
DRUG ABSORPTION;
ENANTIOMER;
LIQUID CHROMATOGRAPHY;
PRIORITY JOURNAL;
STEREOISOMERISM;
TECHNIQUE;
TEMPERATURE;
AMYLOSE;
ANTICHOLESTEREMIC AGENTS;
AZETIDINES;
BETA-LACTAMS;
CARBAMATES;
CHROMATOGRAPHY, HIGH PRESSURE LIQUID;
MOLECULAR CONFORMATION;
PHENYLCARBAMATES;
STEREOISOMERISM;
TEMPERATURE;
THERMODYNAMICS;
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EID: 0035919595
PISSN: 00219673
EISSN: None
Source Type: Journal
DOI: 10.1016/S0021-9673(01)00976-1 Document Type: Article |
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Times cited : (36)
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References (18)
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