Diastereoselectivity in addition of methylmagnesium halide to benzoylformate of chiral 1,1'-binaphthalene-2,2'-diol

Article abstract of DOI:10.1248/cpb.42.957

The Grignard reactions of mono-benzoylformate ester of 1,1'-binaphthalene-2,2'-diol were examined to investigate the complex-induced proximity effect of the phenolic hydroxyl at C-2' under different reaction conditions. This hydroxyl group exerted a significant neighboring group participation in the reaction. The nucleophilic addition reaction proceeded with higher diastereoselectivity than that of a series of sterically similarly sized binaphthyl esters recently reported. The halogen ligand in methyl Grignard reagents plays a crucial role in controlling the degree and sense of diastereoselectivity. A plausible mechanism is also proposed.

Full text of DOI:10.1248/cpb.42.957

NII-Electronic Library Service

NII-Electronic Library Service

NII-Electronic Library Service