E. A. Bercot

发表

Rh(III)-catalyzed C-H activation and double directing group strategy for the regioselective synthesis of naphthyridinones.

T. Hwang, O. Thiel, M. Bio, 2013, Journal of the American Chemical Society.

Further studies with the 2-amino-1,3-thiazol-4(5H)-one class of 11beta-hydroxysteroid dehydrogenase type 1 inhibitors: reducing pregnane X receptor activity and exploring activity in a monkey pharmacodynamic model.

Jiandong Zhang, R. Hungate, M. Véniant, 2008, Journal of medicinal chemistry.

Development of a tandem cyclization mediated by samarium(II) iodide: sequential intramolecular conjugate addition/nucleophilic acyl substitution

D. Jean, E. A. Bercot, Edward P. Cheng, 2006 .

A concise synthesis of eupomatilones 4, 6, and 7 by rhodium-catalyzed enantioselective desymmetrization of cyclic meso anhydrides with organozinc reagents generated in situ.

C. M. Williams, J. B. Johnson, T. Rovis, 2007, Angewandte Chemie.

Diastereoselective palladium-catalyzed alpha-arylation of 4-substituted cyclohexyl esters.

M. Faul, R. Jensen, E. A. Bercot, 2008, Organic letters.

Selective substituent transfer from mixed zinc reagents in Ni-catalyzed anhydride alkylation.

J. B. Johnson, T. Rovis, Jeffrey B. Johnson, 2006, Organic letters.

Decarbonylative cross-coupling of cyclic anhydrides: introducing stereochemistry at an sp3 carbon in the cross-coupling event.

E. O'brien, T. Rovis, E. A. Bercot, 2003, Journal of the American Chemical Society.

A palladium-catalyzed enantioselective alkylative desymmetrization of meso-succinic anhydrides.

T. Rovis, E. A. Bercot, 2004, Journal of the American Chemical Society.

Complementary Diastereoselective Reduction of Cyclic γ-Keto Acids: Efficient Access to Trisubsituted γ-Lactones

T. Rovis, E. A. Bercot, David E. Kindrachuk, 2005 .

2-(S)-phenethylaminothiazolones as potent, orally efficacious inhibitors of 11beta-hydroxysteriod dehydrogenase type 1.

R. Hungate, M. Véniant, Minghan Wang, 2007, Journal of medicinal chemistry.

A mild and efficient catalytic alkylative monofunctionalization of cyclic anhydrides.

T. Rovis, E. A. Bercot, 2002, Journal of the American Chemical Society.

Addressing Process Safety Hazards: Replacement of para-Methoxybenzyl Chloride Leads to a Safer and Shorter Route

Derek B. Brown, R. Milburn, J. Colyer, 2014 .

Selection of a Suitable Physical Form and Development of a Crystallization Process for a PDE10A Inhibitor Exhibiting Enantiotropic Polymorphism

Jodi Liu, Christopher J. Borths, Robert E. Saw, 2015 .

Highly efficient nickel-catalyzed cross-coupling of succinic and glutaric anhydrides with organozinc reagents.

T. Rovis, E. A. Bercot, 2005, Journal of the American Chemical Society.

2‐[2‐(Diphenylphosphanyl)ethyl]pyridine (pyphos)

E. A. Bercot, 2012 .

Ligand-dependent catalytic cycle and role of styrene in nickel-catalyzed anhydride cross-coupling: evidence for turnover-limiting reductive elimination.

G. Coates, T. Rovis, J. Rowley, 2007, Journal of the American Chemical Society.