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Palladium(II)‐Mediated C−H Tritiation of Complex Pharmaceuticals

Angewandte Chemie International Edition, 2018-02, Vol.57 (7), p.1883-1887

International ed. in English, 2018

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Efficient Cross-Coupling of Secondary Alkyltrifluoroborates with Aryl ChloridesReaction Discovery Using Parallel Microscale Experimentation

Journal of the American Chemical Society, 2008-07, Vol.130 (29), p.9257-9259

2008

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Synthesis of Benzo[b]furans via CuI-Catalyzed Ring Closure

Journal of organic chemistry, 2005-08, Vol.70 (17), p.6964-6967

2005

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A Mild and Efficient Synthesis of 4-Quinolones and Quinolone Heterocycles

Journal of organic chemistry, 2007-05, Vol.72 (11), p.4276-4279

2007

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Efficient and General Protocol for the Copper-Free Sonogashira Coupling of Aryl Bromides at Room Temperature

Organic letters, 2003-10, Vol.5 (22), p.4191-4194

2003

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Asymmetric Formal Synthesis of the Long-Acting DPP-4 Inhibitor Omarigliptin

Journal of organic chemistry, 2017-09, Vol.82 (17), p.9023-9029

2017

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A Soluble Copper(I) Source and Stable Salts of Volatile Ligands for Copper-Catalyzed C–X Couplings

Journal of organic chemistry, 2012-09, Vol.77 (17), p.7646-7651

2012

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Enantioselective, Palladium-Catalyzed α-Arylation of N-Boc-pyrrolidine

Journal of the American Chemical Society, 2006-03, Vol.128 (11), p.3538-3539

2006

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Ullmann Diaryl Ether Synthesis: Rate Acceleration by 2,2,6,6-Tetramethylheptane-3,5-dione

Organic letters, 2002-05, Vol.4 (9), p.1623-1626

2002

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Probing in Vitro Release Kinetics of Long-Acting Injectable Nanosuspensions via Flow-NMR Spectroscopy

Molecular pharmaceutics, 2020-02, Vol.17 (2), p.530-540, Article acs.molpharmaceut.9b00958

2020

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Catalyst-Controlled Regioselective Suzuki Couplings at Both Positions of Dihaloimidazoles, Dihalooxazoles, and Dihalothiazoles

Journal of organic chemistry, 2010-03, Vol.75 (5), p.1733-1739

2010

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Expanding the [1,2]-Aryl Migration to the Synthesis of Substituted Indoles

Angewandte Chemie (International ed.), 2008-05, Vol.47 (22), p.4231-4233

2008

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Enantioselective Pd-Catalyzed α-Arylation of N-Boc-Pyrrolidine: The Key to an Efficient and Practical Synthesis of a Glucokinase Activator

Journal of organic chemistry, 2008-07, Vol.73 (13), p.4986-4993

2008

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Synthesis of Vaniprevir (MK-7009): Lactamization To Prepare a 22-Membered Macrocycle

Journal of organic chemistry, 2011-10, Vol.76 (19), p.7804-7815

2011

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Inversion of 1JCC correlations in 1,n-ADEQUATE spectra

Magnetic resonance in chemistry, 2012-08, Vol.50 (8), p.563-568

2012

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Synthesis of ((3R,6R)‑6-Methylpiperidin-3-yl)methanol via Biocatalytic Transamination and Crystallization-Induced Dynamic Resolution

Organic process research & development, 2015-10, Vol.19 (10), p.1418-1423

2015

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Highly enantioselective synthesis of anti aryl β-hydroxy α-amino esters via DKR transfer hydrogenation

Tetrahedron letters, 2011-04, Vol.52 (14), p.1685-1688

2011

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Improved Carbonylation of Heterocyclic Chlorides and Electronically Challenging Aryl Bromides

Organic letters, 2004-06, Vol.6 (13), p.2097-2100

2004

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Development of a pharmaceutical cocrystal of a monophosphate salt with phosphoric acid

Chemical communications (Cambridge, England), 2007-01 (4), p.419-421

2007

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Diastereoselective Friedel−Crafts Alkylation of Indoles with Chiral α-Phenyl Benzylic Cations. Asymmetric Synthesis of Anti-1,1,2-Triarylalkanes

Organic letters, 2008-07, Vol.10 (14), p.3037-3040

2008

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Efficient Synthesis of NK1 Receptor Antagonist Aprepitant Using a Crystallization-Induced Diastereoselective Transformation

Journal of the American Chemical Society, 2003-02, Vol.125 (8), p.2129-2135

2003

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NMR-based approach to the analysis of radiopharmaceuticals: radiochemical purity, specific activity, and radioactive concentration values by proton and tritium NMR spectroscopy

Journal of labelled compounds & radiopharmaceuticals, 2015-06, Vol.58 (7), p.291-298

2015

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Palladium(II)‐Mediated C−H Tritiation of Complex Pharmaceuticals

Angewandte Chemie, 2018-02, Vol.130 (7), p.1901-1905

2018

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Practical Synthesis of A Macrocyclic HCV Protease Inhibitor: A High-Yielding Macrolactam Formation

Organic process research & development, 2014-03, Vol.18 (3), p.423-430

2014

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Highly Regioselective Friedländer Annulations with Unmodified Ketones Employing Novel Amine Catalysts: Syntheses of 2-Substituted Quinolines, 1,8-Naphthyridines, and Related Heterocycles

Journal of organic chemistry, 2003-01, Vol.68 (2), p.467-477

2003

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Palladium(II)‐Mediated C−H Tritiation of Complex Pharmaceuticals

Efficient Cross-Coupling of Secondary Alkyltrifluoroborates with Aryl ChloridesReaction Discovery Using Parallel Microscale Experimentation

Synthesis of Benzo[b]furans via CuI-Catalyzed Ring Closure

A Mild and Efficient Synthesis of 4-Quinolones and Quinolone Heterocycles

Efficient and General Protocol for the Copper-Free Sonogashira Coupling of Aryl Bromides at Room Temperature

Asymmetric Formal Synthesis of the Long-Acting DPP-4 Inhibitor Omarigliptin

A Soluble Copper(I) Source and Stable Salts of Volatile Ligands for Copper-Catalyzed C–X Couplings

Enantioselective, Palladium-Catalyzed α-Arylation of N-Boc-pyrrolidine

Ullmann Diaryl Ether Synthesis: Rate Acceleration by 2,2,6,6-Tetramethylheptane-3,5-dione

Probing in Vitro Release Kinetics of Long-Acting Injectable Nanosuspensions via Flow-NMR Spectroscopy

Catalyst-Controlled Regioselective Suzuki Couplings at Both Positions of Dihaloimidazoles, Dihalooxazoles, and Dihalothiazoles

Expanding the [1,2]-Aryl Migration to the Synthesis of Substituted Indoles

Enantioselective Pd-Catalyzed α-Arylation of N-Boc-Pyrrolidine: The Key to an Efficient and Practical Synthesis of a Glucokinase Activator

Synthesis of Vaniprevir (MK-7009): Lactamization To Prepare a 22-Membered Macrocycle

Inversion of 1JCC correlations in 1,n-ADEQUATE spectra

Synthesis of ((3R,6R)‑6-Methylpiperidin-3-yl)methanol via Biocatalytic Transamination and Crystallization-Induced Dynamic Resolution

Highly enantioselective synthesis of anti aryl β-hydroxy α-amino esters via DKR transfer hydrogenation

Improved Carbonylation of Heterocyclic Chlorides and Electronically Challenging Aryl Bromides

Development of a pharmaceutical cocrystal of a monophosphate salt with phosphoric acid

Diastereoselective Friedel−Crafts Alkylation of Indoles with Chiral α-Phenyl Benzylic Cations. Asymmetric Synthesis of Anti-1,1,2-Triarylalkanes

Efficient Synthesis of NK1 Receptor Antagonist Aprepitant Using a Crystallization-Induced Diastereoselective Transformation

NMR-based approach to the analysis of radiopharmaceuticals: radiochemical purity, specific activity, and radioactive concentration values by proton and tritium NMR spectroscopy

Palladium(II)‐Mediated C−H Tritiation of Complex Pharmaceuticals

Practical Synthesis of A Macrocyclic HCV Protease Inhibitor: A High-Yielding Macrolactam Formation

Highly Regioselective Friedländer Annulations with Unmodified Ketones Employing Novel Amine Catalysts: Syntheses of 2-Substituted Quinolines, 1,8-Naphthyridines, and Related Heterocycles

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