Studies of enantiomeric separations are reported, specifically the dir
ect chromatographic separation of enantiomers using a chiral stationar
y phase by molecular topology. The results obtained show good correlat
ion equations for the capacity factor, k', and the separation factor,
alpha, for different set of compounds (hydantoins, aromatic alpha-amin
o acids and arylamides). Such equations may be useful for the selectio
n of the optimum stationary and mobile phases for the separation of en
antiomers. Further, the correlation between topological descriptors an
d performance in chiral separations opens up a new approach to the des
ign of chiral stationary phases.