Asymmetric Hydrogenation of Racemic 6-Aryl 1,4-Dioxaspiro[4.5]decan-7-ones to Functionalized Chiral ß-Aryl Cyclohexanols via a Dynamic Kinetic Resolution.

A ruthenium-catalyzed asymmetric hydrogenation method for the synthesis of functionalized ß-aryl cyclohexanols is described. With chiral spiro ruthenium catalyst (Ra,S,S)-5c, a series of racemic α-aryl cyclohexanones bearing a ß-monoethylene ketal group were hydrogenated to the corresponding functionalized ß-aryl cyclohexanols in high yields with enantioselectivity of up to 99% ee via a dynamic kinetic resolution. This protocol can be conducted on a decagram scale and provide potential approaches for the synthesis of optically active and densely functionalized aryl cyclohexanols.