Copper-Catalyzed Asymmetric Synthesis of Silicon-Stereogenic Benzoxasiloles

A Cu-catalyzed asymmetric synthesis of silicon-stereogenic benzoxasiloles has been realized via intramolecular Si-O coupling of [2-(hydroxymethyl)phenyl]silanes. Cu(I)/difluorphos is found to be an efficient catalytic system for enantioselective Si-C bond cleavage and Si-O bond formation. In addition, kinetic resolution of racemic substituted [2-(hydroxymethyl)phenyl]silanes using Cu(I)/ PyrOx (pyridine-oxazoline ligands) as the catalytic system is developed to afford carbon- and silicon-stereogenic benzoxasiloles. Ring-opening reactions of chiral benzoxasiloles with organolithiums and Grignard reagents yield various enantioenriched functionalized tetraorganosilanes. A Cu-catalyzed asymmetric synthesis of silicon-stereogenic benzoxasiloles has been realized via the intramolecular Si-O coupling of [2-(hydroxymethyl)phenyl]silanes using Cu(I)/difluorphos as the efficient catalytic system. Kinetic resolution of racemic substituted [2-(hydroxymethyl)phenyl]silanes using Cu(I)/PyrOx as the catalytic system was also achieved to afford carbon- and silicon-stereogenic benzoxasilole species.+image