A hybrid Au/Ru catalyst for sequential alkyne hydration/asymmetric transfer hydrogenation reactions†
Abstract
The utilization of organic/inorganic core/shell support materials by compartmentalizing of Au(I)/Ru(II) catalysts has led to the formation of chiral alcohol derivatives from alkynes via sequential alkyne hydration and asymmetric transfer hydrogenation reactions. A Ru(II) complex was supported on chiral ligand end-capped amphiphilic ROMP polymers. The micellar Ru(II) catalyst was coated with a mesoporous silica shell to produce a secondary compartment where an IPrAuCl complex was confined in mesopores of silica gel through post-pore size reduction. A variety of alkynes were converted to chiral alcohol derivatives in quantitative yields with high enantioselectivity in a MeOH/H2O mixture using sequential alkyne hydration/asymmetric transfer hydrogenation reactions.