130179-66-7Relevant academic research and scientific papers
ASYMMETRIC 1,3-DIPOLAR CYCLOADDITIONS OF AZOMETHINE YLIDES WITH A CHIRAL ELECTRON-DEFICIENT OLEFINIC DIPOLAROPHILE
Kanemasa, Shuji,Yamamoto, Hidetoshi
, p. 3633 - 3636 (1990)
The first example of efficient asymmetric 1,3-dipolar cycloadditions of azomethine ylides is presented, where reactive N-metalated azomethine ylides and the α,β-unsaturated ester with a chiral perhydropyrroloimidazol-3-yl moiety at the β-position h
Asymmetric cycloaddition of N-metalated azomethine ylides with the optically active α,β-unsaturated esters derived from α-amino acids
Kanemasa, Shuji,Yamamoto, Hidetoshi,Wada, Eiji,Sakurai, Tosio,Urushido, Kunio
, p. 2857 - 2865 (2007/10/02)
α,β-Unsaturated esters bearing a chiral oxazolidine or perhydropyrrolo[1,2-c]imidazole auxiliary at the β-position have been prepared and applied to the cycloadditions with N-metalated azomethine ylides derived from a-(benzylideneamino) esters. These reac
