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