SOME RECENT HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY SEPARATIONS OF THEENANTIOMERS OF PHARMACEUTICALS AND OTHER COMPOUNDS USING THE WHELK-O 1 CHIRAL STATIONARY-PHASE
Cj. Welch et al., SOME RECENT HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY SEPARATIONS OF THEENANTIOMERS OF PHARMACEUTICALS AND OTHER COMPOUNDS USING THE WHELK-O 1 CHIRAL STATIONARY-PHASE, Journal of chromatography, 758(1), 1997, pp. 93-98
Citations number
23
Categorie Soggetti
Chemistry Analytical","Biochemical Research Methods
The Whelk-O 1 chiral stationary phase is generally useful for the chro
matographic separation of the enantiomers of many classes of analytes
including aryl propionic acid non-steroidal anti-inflammatory drugs, a
ryl epoxides, sulfoxides, alcohols, amides and esters. We herein repor
t some additional recent enantioseparations obtained with this column,
including a number of pharmaceuticals such as thalidomide, nicardipin
e, isradipine, mephenytoin, nirvanol, cyclandelate, bendroflumethiazid
e, bupivicaine, tolperisone, proglumide, tropicamide and indapamide. T
he separation of the enantiomers of a collection of additional analyte
s is also reported, including several compounds containing basic nitro
gen, a heretofore difficult class of compounds to resolve with this co
lumn.