1221726-75-5Relevant articles and documents
Catalytic asymmetric hydrophosphinylation of α,β-unsaturated N -acylpyrroles: Application of dialkyl phosphine oxides in enantioselective synthesis of chiral phosphine oxides or phosphines
Zhao, Depeng,Mao, Lijuan,Wang, Yuan,Yang, Dongxu,Zhang, Quanliang,Wang, Rui
supporting information; scheme or table, p. 1880 - 1882 (2010/09/05)
Dialkyl phosphine oxides were introduced in catalytic asymmetric transformations for the first time. An unprecedented phospha-Michael reaction of dialkyl phosphine oxide with α,β-unsaturated N-acylpyrroles was disclosed. Excellent enantioselectivities (94→99% ee) and chemical yields (up to 99%) were achieved with a broad substrate scope of the N-acylpyrroles. Importantly, pyridine was found to be critical to achieve good results for the present reaction.