Enantioselective Nitrone Cycloadditions of α,β-Unsaturated 2-Acyl Imidazoles Catalyzed by Bis(oxazolinyl)pyridine−Cerium(IV) Triflate Complexes David A. Evans Hyun-Ji Song Keith R. Fandrick 10.1021/ol061223i.s001 https://acs.figshare.com/articles/dataset/Enantioselective_Nitrone_Cycloadditions_of_Unsaturated_2_Acyl_Imidazoles_Catalyzed_by_Bis_oxazolinyl_pyridine_Cerium_IV_Triflate_Complexes/3069961 Enantioselective nitrone cycloadditions with β-substituted α,β-unsaturated 2-acyl imidazoles catalyzed by bis(oxazolinyl)pyridine−cerium(IV) triflate complexes <b>1</b> have been reported. The isoxazolidine products were efficiently transformed into densely functionalized β‘-hydroxy-β-amino acid derivatives. 2006-07-20 00:00:00 isoxazolidine products functionalized Enantioselective Nitrone Cycloadditions acid Imidazole derivative Acyl cycloaddition complex Triflate Bis imidazole acyl bi triflate Catalyzed nitrone Unsaturated ComplexesEnantioselective hydroxy