S. Caron

发表

Large-scale oxidations in the pharmaceutical industry.

D. Ripin, S. Caron, R. W. Dugger, 2006, Chemical reviews.

Efficient synthesis of [6-chloro-2-(4-chlorobenzoyl)-1H-indol-3-yl]-acetic acid, a novel COX-2 inhibitor.

S. Caron, R. Stevens, Kazunari Nakao, 2003, The Journal of organic chemistry.

Synthesis of 2,3,4,5-tetrahydro-1,5-methano-1H-3-benzazepine via oxidative cleavage and reductive amination strategies

S. Caron, Enrique Vazquez, J. Coe, 2004 .

Where Does the Fluorine Come From? A Review on the Challenges Associated with the Synthesis of Organofluorine Compounds

S. Caron, 2020 .

Synthesis of the kappa-agonist CJ-15,161 via a palladium-catalyzed cross-coupling reaction.

Arun K. Ghosh, S. Caron, T. Watson, 2002, Chemical communications.

New Synthetic Route to a Dipeptidyl Peptidase-4 Inhibitor

S. Caron, D. Lafrance, 2012 .

Functional analysis of the NPDC-1 gene.

S. Caron, C. Evrard, P. Rouget, 2004, Gene.

Development of two synthetic routes to CE-178,253, a CB1 antagonist for the treatment of obesity

Arun K. Ghosh, S. Caron, J. A. Ragan, 2009 .

Commercial Route Research and Development for SGLT2 Inhibitor Candidate Ertugliflozin

Teresa W. Makowski, Brian P. Jones, Nga M. Do, 2014 .

New Ligands for Nickel Catalysis from Diverse Pharmaceutical Heterocycle Libraries

D. Weix, E. Hansen, S. Caron, 2016, Nature chemistry.

Preparation of a Corticotropin-Releasing Factor Antagonist by Nucleophilic Aromatic Substitution and Copper-Mediated Ether Formation†

Nga M. Do, S. Caron, D. Whritenour, 2009 .

A practical, efficient, and rapid method for the oxidation of electron deficient pyridines using trifluoroacetic anhydride and hydrogen peroxide–urea complex

Nga M. Do, S. Caron, J. Sieser, 2000 .

An Efficient and Cost-Effective Synthesis of 2-Phenyl-3-aminopyridine

S. Caron, D. Bogle, Stephen S. Massett, 2001 .

A Versatile and Efficient Synthesis of Substituted 1H-Indazoles

S. Caron, Enrique Vazquez, 1999 .

A Practical, Efficient, and Rapid Method for the Oxidation of Electron-Deficient Pyridines Using Trifluoroacetic Anhydride and Hydrogen Peroxide—Urea Complex.

Nga M. Do, S. Caron, J. Sieser, 2000 .

Total synthesis of zaragozic acid A (squalestatin S1). Synthesis of the relay compound

S. Caron, C. Heathcock, D. Stoermer, 1996 .

Nucleophilic Aromatic Substitution

S. Caron, E. McInturff, 2020, Practical Synthetic Organic Chemistry.

Development of a Practical and Convergent Process for the Preparation of Sulopenem

Steven J. Brenek, N. Ide, J. Teixeira, 2012 .

Directed Ortho Metalation of Neopentyl Benzoates with LDA: Preparation of Arylboronic Acids

S. Caron, J. Hawkins, 1998 .

Alternative Biarylphosphines for Use in the Palladium-Catalyzed Amination of Aryl Halides

Nga M. Do, S. Caron, R. Singer, 2003 .

Preparation and utility of trihaloethyl imidates: useful reagents for the synthesis of amidines.

Arun K. Ghosh, S. Caron, Lulin Wei, 2010, The Journal of organic chemistry.

Large‐Scale Oxidations in the Pharmaceutical Industry

D. Ripin, S. Caron, R. W. Dugger, 2006 .

Development of a Second-Generation Process to Antibacterial Candidate Sulopenem

Brian P. Jones, Steven J. Brenek, S. Caron, 2012 .

Preparation and utility of trihaloethyl imidates: useful reagents for the synthesis of amidines.

Arun K. Ghosh, S. Caron, Lulin Wei, 2010, The Journal of organic chemistry.

Preparation of Tertiary Benzylic Nitriles from Aryl Fluorides

S. Caron, and Enrique Vazquez, J. M. Wojcik, 2000 .

The Synthesis of a Selective PDE4/TNFα Inhibitor

S. Caron, Enrique Vazquez, 2001 .

Process Research and Development of an NK-1 Receptor Antagonist. Enantioselective Trifluoromethyl Addition to a Ketone in the Preparation of a Chiral Isochroman

Nga M. Do, S. Caron, Enrique Vazquez, 2007 .

Process Research and Scale-up of the κ-Opioid Receptor Agonist CJ-15,161 Drug Candidate

Nga M. Do, Arun K. Ghosh, S. Caron, 2006 .

Preparation of Substituted Benzimidazoles and Imidazopyridines Using 2,2,2-Trichloroethyl Imidates

Brian P. Jones, S. Caron, Lulin Wei, 2012 .

Total Synthesis of Zaragozic Acid A (Squalestatin S1). Degradation to a Relay Compound and Reassembly of the Natural Product

S. Caron, C. Heathcock, D. Stoermer, 1996 .

Total Synthesis of Zaragozic Acid A (Squalestatin S1) (I). Degradation to a Relay Compound (II) and Reassembly of the Natural Product.

S. Caron, C. Heathcock, D. Stoermer, 1997 .

SYNTHESIS OF 1-SUBSTITUTED AND 1,4-DISUBSTITUTED 2,3-DI-O-BENZYL-1,6-ANHYDROGALACTOFURANOSES

S. Caron, C. Heathcock, A. McDonald, 1995 .

Approach to the synthesis of candelabrone and synthesis of 3,7-diketo- 12-hydroxyabieta-8,11,13-triene

S. Caron, R. H. Burnell, 1992 .

The application of structure-based assessment to support safety and chemistry diligence to manage genotoxic impurities in active pharmaceutical ingredients during drug development.

Nigel Greene, Warren W Ku, Krista L Dobo, 2006, Regulatory toxicology and pharmacology : RTP.

Nucleophilic Aromatic Substitution of Aryl Fluorides by Secondary Nitriles: Preparation of 2‐(2‐Methoxyphenyl)‐2‐Methylpropionitrile

S. Caron, Enrique Vazquez, J. M. Wojcik, 2003 .

Pharmaceutical process chemistry: evolution of a contemporary data-rich laboratory environment.

Nicholas Murray Thomson, S. Caron, N. Thomson, 2015, The Journal of organic chemistry.

An improved synthesis of 1,6-anhydro-2,3-di-O-benzyl-β-d-xylo-hexopyranos-4-ulose

S. Caron, C. Heathcock, A. McDonald, 1996 .

Synthesis of Aromatic Diterpenes Synthesis of 12-Hydroxy-abieta-8,11,13-trien-3,7-dione

S. Caron, R. H. Burnell, 1991 .

Enantioselective addition of a trifluoromethyl anion to aryl ketones and aldehydes

Nga M. Do, S. Caron, Alexandre Larivée, 2003 .

Pharmaceutical process chemistry: evolution of a contemporary data-rich laboratory environment.

S. Caron, N. Thomson, 2015, The Journal of organic chemistry.

Honoring 25 Years of the Buchwald–Hartwig Amination

S. Caron, 2019, Organic Process Research & Development.

Reductions

Nathan D. Ide, S. Caron, S. G. Ruggeri, 2020, Practical Synthetic Organic Chemistry.