Palladium(II)-Catalyzed Enantioselective C(sp(3))–H Activation Using a Chiral Hydroxamic Acid Ligand

[Image: see text] An enantioselective method for Pd(II)-catalyzed cross-coupling of methylene β-C(sp(3))–H bonds in cyclobutanecarboxylic acid derivatives with arylboron reagents is described. High yields and enantioselectivities were achieved through the development of chiral mono-N-protected α-amino-O-methylhydroxamic acid (MPAHA) ligands, which form a chiral complex with the Pd(II) center. This reaction provides an alternative approach to the enantioselective synthesis of cyclobutanecarboxylates containing α-chiral quaternary stereocenters. This new class of chiral catalysts also show promises for enantioselective β-C(sp(3))–H activation of acyclic amides.