S. Wagaw

发表

Discovery of adamantane ethers as inhibitors of 11beta-HSD-1: Synthesis and biological evaluation.

K. Longenecker, Jyoti R. Patel, H. Sham, 2007, Bioorganic & medicinal chemistry letters.

Rational Development of Practical Catalysts for Aromatic Carbon−Nitrogen Bond Formation

John P. Wolfe, Stephen L. Buchwald, S. Buchwald, 1998 .

Rational Development of Practical Catalysts for Aromatic Carbon—Nitrogen Bond Formation

S. Buchwald, J. Wolfe, S. Wagaw, 1999 .

The Synthesis of Aminopyridines: A Method Employing Palladium- Catalyzed Carbon-Nitrogen Bond Formation.

S. Buchwald, S. Wagaw, 1997 .

Validation of diacyl glycerolacyltransferase I as a novel target for the treatment of obesity and dyslipidemia using a potent and selective small molecule inhibitor.

A. Souers, G. Diaz, H. Sham, 2008, Journal of medicinal chemistry.

Palladium-Catalyzed Amination of Aryl Bromides: Use of Phosphinoether Ligands for the Efficient Coupling of Acyclic Secondary Amines

S. Buchwald, S. Wagaw, J. Marcoux, 1997 .

The Synthesis of Aminopyridines: A Method Employing Palladium-Catalyzed Carbon-Nitrogen Bond Formation.

S. Buchwald, S. Wagaw, S. Buchwald, 1996, The Journal of organic chemistry.

An Improved Catalyst System for Aromatic Carbon−Nitrogen Bond Formation: The Possible Involvement of Bis(Phosphine) Palladium Complexes as Key Intermediates

John P. Wolfe, Stephen L. Buchwald, S. Buchwald, 1996 .

Improved synthesis of 3-substituted-4-amino-[3,2-c]-thienopyridines.

R. Rickert, S. Wagaw, Kenneth M. Engstrom, 2009, The Journal of organic chemistry.

Palladium-Catalyzed Coupling of Optically Active Amines with Aryl Bromides

S. Buchwald, S. Wagaw, R. Rennels, 1997 .

A Palladium-Catalyzed Method for the Preparation of Indoles via the Fischer Indole Synthesis

Stephen L. Buchwald, S. Buchwald, S. Wagaw, 1999 .

A Palladium-Catalyzed Strategy for the Preparation of Indoles: A Novel Entry into the Fischer Indole Synthesis

S. Buchwald, S. Wagaw, Bryant H. Yang, 1998 .

Aminopiperidine indazoles as orally efficacious melanin concentrating hormone receptor-1 antagonists.

Ju Gao, Anil Vasudevan, John K Lynch, 2005, Bioorganic & medicinal chemistry letters.

Development of a catalytic enantioselective conjugate addition of 1,3-dicarbonyl compounds to nitroalkenes for the synthesis of endothelin-A antagonist ABT-546. Scope, mechanism, and further application to the synthesis of the antidepressant rolipram.

S. King, D. Barnes, S. Wittenberger, 2002, Journal of the American Chemical Society.

Process Development of a Diacyl Glycerolacyltransferase-1 Inhibitor

Brian J. Kotecki, A. Souers, P. Kym, 2010 .

Development of a Scalable Synthesis of Dipeptidyl Peptidase-4 Inhibitor ABT-279

Brian J. Kotecki, A. Sheikh, L. Bhagavatula, 2009 .

Palladium‐Catalyzed Coupling of Optically Active Amines with Aryl Bromides.

S. Buchwald, S. Wagaw, R. Rennels, 1997 .

Gram scale synthesis of the glucuronide metabolite of ABT-724.

S. Wagaw, Kenneth M. Engstrom, A. Stewart, 2006, The Journal of organic chemistry.

Chlorination at the 8-Position of a Functionalized Quinolone and the Synthesis of Quinolone Antibiotic ABT-492

M. J. Peterson, Elaine C. Lee, J. Tedrow, 2006 .

A Convergent Process for the Preparation of Adamantane 11-β-HSD-1 Inhibitors

J. Tolle, S. Wagaw, Kenneth M. Engstrom, 2008 .

Screening for cardiovascular safety: a structure-activity approach for guiding lead selection of melanin concentrating hormone receptor 1 antagonists.

Ju Gao, Anil Vasudevan, John K Lynch, 2006, Journal of medicinal chemistry.