TETRAHEDRON ASYMMETRY, vol.17, pp.742-746, 2006 (SCI-Expanded)
Novel norephedrine-based chiral ligands with multiple stereogenic centers were conveniently prepared from norephedrine
and N-substituted pyrrole. These novel chiral ligands were used to catalyze the enantioselective addition of diethylzinc to aldehydes
and to chalcone in high yields and with good to high enantioselectivities. The absolute configuration of products was found to be
affected by the stereogenic centers on the norephedrine part of the novel chiral ligands.