Efficient reduction of mono- and disubstituted norbornyl α-diketones with zinc in [bmimBF4]:[H2O] to afford the corresponding acyloins in excellent yields and diastereoselectivities is described. In case of the monosubstituted norbornyl α-diketones, very high regioselectivities ranging from 90:10 to 100:0, in favor of diastereomer possessing endohydroxyl diagonal to endo-substituent were observed.