Utilization of optically active secondary phosphine–boranes: synthesis of P-chiral diphosphines and their enantioinduction ability in rhodium-catalyzed asymmetric hydrogenation

Both enantiomers of tert-butylmethylphosphine–borane have been used for the synthesis of P-chiral diphosphines and/or their borane complexes. The enantiopure borane complex of 1,2-bis(tert-butylmethylphosphino)ethane (t-Bu-BisP∗) was prepared in high yield from the secondary phosphine–borane and 1,2-dichloroethane. A mono-chelated Rh-complex of t-Bu-MiniPHOS was prepared and its catalytic activity was examined in the asymmetric hydrogenation of some representative functionalized alkenes. Synthesis of three new P-chiral phosphine ligands with quinoline or quinoxaline backbone is also described together with their enantioinduction ability.

Figure optionsDownload high-quality image (155 K)Download as PowerPoint slide