Enantioselective bromination/semipinacol rearrangement for the synthesis of β-bromoketones containing an all-α-carbon quaternary center.
Chem. Sci. 2011, 12, 1839.
Direct sp3 α-C-H activation and functionalization of alcohol and ether.
Chem. Soc. Rev. 2011, 40, 1937.
Organocatalytic asymmetric halogenation/semipinacol rearrangement: Highly efficient synthesis of chiral α-oxa-quaternary β-haloketones.
J. Am. Chem. Soc. 2011, 133, 8818.
