Design and synthesis of novel 1,3-diene bridged chiral atropoisomeric diphosphine ligands for asymmetric hydrogenation of a-dehydro amino ketones

A series of novel atropisomeric diphosphine ligands termed TanPhos were designed and synthesized, which has a smaller bite angle compared with that of other ligands such as BINAP. TanPhos showed high reactivity and enantioselectivity in the rhodium-catalyzed asymmetric hydrogenation of a-dehydro amino ketones, and up 99% yield and 99% ee were obtained for a wide range of chiral & alpha;-amino ketones.

Automated summary

A series of novel atropisomeric diphosphine ligands termed TanPhos with a smaller bite angle were synthesized and designed. TanPhos exhibited high reactivity and enantioselectivity in the rhodium-catalyzed asymmetric hydrogenation of α-dehydro amino ketones, achieving up to 99% yield and 99% ee for a wide range of chiral α-amino ketones.