Aydin, A. E.2024-09-182024-09-1820201070-42801608-3393https://doi.org/10.1134/S1070428020070271https://hdl.handle.net/20.500.12483/7982Chiral oxazoline ligands containing an aromatic ring were prepared from norephedrine and pyrrole-2-carbonitrile or 2-hydroxybenzoyl chloride. The synthesized ligands were used in the copper-catalyzed asymmetric addition of diethylzinc to aromatic aldehydes to provide optically active 1-arylpropan-1-ols with high conversion (92%) and enantioselectivity (up to 99%ee).eninfo:eu-repo/semantics/closedAccessasymmetric catalysisenantioselective synthesischiral oxazoline-based ligands12-additionEnantioselective Addition of Diethylzinc to Aromatic Aldehydes Using Chiral Oxazoline-Based LigandsArticle5671304131210.1134/S1070428020070271WOS:000567893800027Q4