50789-50-9Relevant articles and documents
Diastereoselective addition of α-metalated sulfoxides to imines revisited: Mechanism, computational studies, and the effect of external chiral ligands
Pedersen, Brian,Rein, Tobias,Sotofte, Inger,Norrby, Per-Ola,Tanner, David
, p. 885 - 898 (2007/10/03)
Some new results on asymmetric synthesis via the addition of α-metalated methyl tolyl sulfoxides to imines are presented. Good diastereoselectivity (up to >98% d.e. for product 3g) can be obtained under conditions of kinetic control (short reaction time,
Diastereoselective Kinetically and Thermodynamically Controlled Additions of (R)-(+)-Methyl p-Tolyl Sulphoxide Anion to Imines (Tolyl = C6H4Me)
Pyne, Stephen G.,Dikic, Branko
, p. 826 - 827 (2007/10/02)
The anion of (R)-(+)-methyl p-tolyl sulphoxide reacts diastereoselectively with imines to give chiral β-amino sulphoxides.