M. Bidlo-igloy et P. Matyus, Enantiomeric separation of optically active pyridazinone derivatives by chiral HPLC, J PHARM B, 19(3-4), 1999, pp. 487-490
Several 4,5-disubstituted 3(2H)-pyridazinone derivatives containing 2-hydro
xymethylpyrrolidino moiety as a chiral building block were synthetized. Sep
aration of enantiomers was carried out by chiral HPLC on Chiralcel OJ and O
F columns. Mobile phases consisted of hexane, ethanol and 2-propanol. Chira
lcel OJ column was capable of separating most of the enantiomeric pairs. Fo
r one type of compound, Chiralcel OF column was used for separation. (C) 19
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