The kinetic resolution of oxiranes by use of chiral Lewis acid catalys
ts is described. Improved stereoselectivities are observed in the nucl
eophilic ring opening of oxiranes with secondary amines. For the first
time the enantioselective insertion of CO2 into the oxirane ring form
ing enantiomerically enriched 1,3-dioxolanones was achieved applying c
hirally modified Zr- and Ti-complexes.