The stereoselective synthesis of functionalized vicinal diamine systems by the double allylation reactions of "protected" 1,2-bis-imine precursors

Article abstract of DOI:10.1016/S0040-4039(00)79412-3

A diastereoselective synthesis of vicinal diamines via the reactions of allylic Grignard reagents with readily available "protected" 1,2-bisimines has been developed. This method has been extended to preparing optically pure diamines by the use of chiral