Asymmetric Intramolecular Arylcyanation of Unactivated Olefins via C–CN Bond Activation
Watson, M. P.; Jacobsen, E. N.
J. Am. Chem. Soc. 2008, 130(38), 12594–12595.

Kinetic and Computational Analysis of the Palladium(II)-Catalyzed Asymmetric Allylic Trichloroacetimidate Rearrangement: Development of a Model for Enantioselectivity
Watson, M. P.; Overman, L. E.; Bergman, R. G.
J. Am. Chem. Soc. 2007, 129(16), 5031–5044.

Preparation of the COP Catalysts: [(S)-COP-OAc]2, [(S)-COP-Cl]2, and (S)-COP-hfacac
Anderson, C. E.; Kirsch, S. F.; Overman, L. E.; Richards, C. J.; Watson, M. P.
Org. Synth. 2007, 84, 148–155.

Preparation of (eta5-(S)-2-(4-methylethyl)oxazolinylcyclopentadienyl)-(eta4-tetraphenylcyclobutadiene)cobalt
Anderson, C. E.; Overman, L. E.; Richards, C. J.; Watson, M. P.; White, N.
Org. Synth. 2007, 84, 139–147.

Asymmetric Rearrangement of Allylic Trichloroacetimidates: Preparation of (S)-2,2,2,-Trichloro-N-(1-propylallyl)acetamide
Anderson, C. E.; Overman, L. E.; Watson, M. P.
Org. Synth. 2005, 82, 134–139.

Monomeric Cobalt Oxazoline Palladacycles (COP). Useful Catalysis for Catalytic Asymmetric Rearrangement of Allylic Trichloroacetimidates
Kirsch, S. F.; Overman, L. E.; Watson, M. P.
J. Org. Chem. 2004, 69(23), 8101–8104.

Catalytic Asymmetric Rearrangement of Allylic N-Aryl Trifluoroacetimidates. A Useful Method for Transforming Prochiral Allylic Alcohols to Chiral Allylic Amines
Overman, L. E.; Owen, C. E.; Pavan, M. M.; Richards, C. J.
Org. Lett. 2003, 5(11), 1809–1812.