A. Vanoverbeke et al., SEPARATION OF 2-ARYLPROPIONIC ACIDS ON A CELLULOSE-BASED CHIRAL STATIONARY-PHASE BY RP-HPLC, Journal of pharmaceutical and biomedical analysis, 12(7), 1994, pp. 901-909
The enantiomers of eight 2-arylpropionic acids, a group of chiral non
steroidal antiinflammatory drugs, were resolved as their benzylamide d
erivatives on a high-performance liquid chromatographic chiral station
ary phase consisting of a covalently bound tris (4-methylbenzoate) cel
lulose layer on silica gel. The column was used under reversed-phase c
onditions using methanol as the main mobile phase component, with a pe
rchlorate buffer pH 2.0. A compromise for derivatization with a water
soluble carbodiimide and 1-hydroxybenzotriazole of a group of eight an
alytes was obtained. The derivatives were identified by IR- and MS-spe
ctroscopy.