Direct high-performance liquid chromatographic separation of the enantiomers of venlafaxine and 11 analogs usingamylose-derived chiral stationary phases

Chirality

Volumn 21, Issue 6, 2009, Pages 569-577

  Caccamese, Salvatore ^a   Bianca, Salvatore ^a   Carter, Guy T ^b  

^a UNIVERSITY OF CATANIA   (Italy)

^b WYETH RESEARCH   (United States)

Author keywords

aminoalcohols; Alcoholic modifers; Antidepressant drugs; Basic and acidic additives; Enantiomers separation; Polysaccharide chiral stationary phases

Indexed keywords

2 PROPANOL; ALCOHOL; AMYLOSE; CELLULOSE TRIS(3,5 DIMETHYLPHENYLCARBAMATE); DIETHANOLAMINE; TRIFLUOROACETIC ACID; VENLAFAXINE; CYCLOHEXANOL DERIVATIVE;

ACIDITY; ALKALINITY; ARTICLE; BIOSEPARATION; CHIRALITY; CONTROLLED STUDY; DRUG FORMULATION; ELECTRON; ENANTIOMER; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; MATERIAL STATE; PHASE TRANSITION; PRIORITY JOURNAL; SOLUBILITY; CHEMISTRY; ISOLATION AND PURIFICATION; METHODOLOGY; PH; STEREOISOMERISM;

2-PROPANOL; AMYLOSE; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; CYCLOHEXANOLS; ETHANOL; HYDROGEN-ION CONCENTRATION; STEREOISOMERISM;

EID: 67649415479     PISSN: 08990042     EISSN: 1520636X     Source Type: Journal    
DOI: 10.1002/chir.20633     Document Type: Article

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