摘要
Chiral monodentate phosphoramidite ligands were conveniently prepared from 1,1＇-bi-2-naphthol （BINOL） and （S）-pyrrolidine in good yields, which were effective chiral ligands in the enantioselective rhodium-catalyzed hydrogenation of dehydroamino esters and enamides at low hydrogenation pressure. High conversion rate （up to 99% for dehydroamino esters and enamides） and good enantioselectivity （up to 96.3% ee for dehy- droamino esters and 91.7% ee for enamides） were obtained.
Chiral monodentate phosphoramidite ligands were conveniently prepared from 1,1＇-bi-2-naphthol （BINOL） and （S）-pyrrolidine in good yields, which were effective chiral ligands in the enantioselective rhodium-catalyzed hydrogenation of dehydroamino esters and enamides at low hydrogenation pressure. High conversion rate （up to 99% for dehydroamino esters and enamides） and good enantioselectivity （up to 96.3% ee for dehy- droamino esters and 91.7% ee for enamides） were obtained.
基金
Supported by the National Natural Science Foundation of China (20572101)
