George Zhou

Mitsunobu Inversion of a Secondary Alcohol with Diphenylphosphoryl azide. Application to the Enantioselective Multikilogram Synthesis of a HCV Polymerase Inhibitor

Jeremy P. Scott, N. Bremeyer, Robert D. Wilson, 2011 .

Development of a Fit-for-Purpose Large-Scale Synthesis of an Oral PARP Inhibitor

Daniel J. Muzzio, Paul Fernandez, P. Sajonz, 2011 .

Development of a Practical Synthesis of Stearoyl-CoA Desaturase (SCD1) Inhibitor MK-8245

Paul Fernandez, G. Hughes, M. Girardin, 2011 .

Enantioselective, palladium-catalyzed α-arylation of N-Boc pyrrolidine: in situ react IR spectroscopic monitoring, scope, and synthetic applications.

P. O’Brien, G. Barker, A. Klapars, 2011, The Journal of organic chemistry.

An Efficient Synthesis of a Dual PPAR α/γ Agonist and the Formation of a Sterically Congested α-Aryloxyisobutyric Acid via a Bargellini Reaction

John Y. L. Chung, R. Cvetovich, J. Amato, 2005 .

Catalytic, Enantioselective Synthesis of Taranabant, a Novel, Acyclic Cannabinoid-1 Receptor Inverse Agonist for the Treatment of Obesity

Alex M. Chen, Jeff Strine, Cheng-yi Chen, 2007 .

Synthesis of a NO-releasing prodrug of rofecoxib.

D. Conlon, J. Mcnamara, Yao‐Jun Shi, 2006, The Journal of organic chemistry.