The enantiomers of tetramisole were produced by partial diastereomeric salt formation with O, O′-dibenzoyl-(2R, 3R)-tartaric acid monohydrate and subsequent supercritical fluid extraction (SFE) of the unreacted enantiomers in the presence of an achiral support. The effect of the activated carbon and Perfil 100™ on the efficiency of chiral separation were studied. The kinetics of the process was found to be an important factor affecting ...