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Streamlined Synthesis of the Bippyphos Family of Ligands and Cross-Coupling Applications

Organic process research & development, 2008-05, Vol.12 (3), p.480-489

2008

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Development of an Efficient Pd-Catalyzed Coupling Process for Axitinib

Organic process research & development, 2014-01, Vol.18 (1), p.266-274

2014

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Development of nonproprietary phosphine ligands for the Pd-catalyzed amination reaction

Tetrahedron letters, 2006-05, Vol.47 (22), p.3727-3731

2006

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Ir-Catalyzed Borylation as an Efficient Route to a Nicotine Hapten

Organic process research & development, 2018-04, Vol.22 (4), p.527-534

2018

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

Organic process research & development, 2007-11, Vol.11 (6), p.1015-1024

2007

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Blei

Fresenius' Zeitschrift für analytische Chemie, 1930-11, Vol.80 (11-12), p.447-455

1930

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Palladium-Catalyzed Synthesis of N-Aryloxazolidinones from Aryl Chlorides

Organic letters, 2003-06, Vol.5 (13), p.2207-2210

2003

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Development of the Commercial Route for the Manufacture of a 5‑Lipoxygenase Inhibitor PF-04191834

Organic process research & development, 2015-12, Vol.19 (12), p.1944-1953

2015

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Synthesis of Filibuvir. Part I. Diastereoselective Preparation of a β‑Hydroxy Alkynyl Oxazolidinone and Conversion to a 6,6-Disubstituted 2H‑Pyranone

Organic process research & development, 2014-01, Vol.18 (1), p.26-35

2014

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Cu-Catalyzed N-Arylation of Oxazolidinones: An Efficient Synthesis of the κ-Opioid Receptor Agonist CJ-15161

Journal of organic chemistry, 2006-02, Vol.71 (3), p.1258-1261

2006

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

Tetrahedron letters, 2000-04, Vol.41 (14), p.2299-2302

2000

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

Organic process research & development, 2009-03, Vol.13 (2), p.324-330

2009

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Synthesis of Filibuvir. Part II. Second-Generation Synthesis of a 6,6-Disubstituted 2H‑Pyranone via Dieckmann Cyclization of a β‑Acetoxy Ester

Organic process research & development, 2014-01, Vol.18 (1), p.36-44

2014

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Cu-catalyzed N-arylation of oxazolidinones : An efficient synthesis of the k-opioid receptor agonist CJ-15161

Journal of organic chemistry, 2006-02, Vol.71 (3), p.1258-1261

2006

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Synthesis of a Bicyclic Piperazine from l-Aspartic Acid and Application of a Fluoride-Promoted SNAr Coupling

Organic process research & development, 2011-11, Vol.15 (6), p.1328-1335

2011

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Synthesis of a Bicyclic Piperazine from l -Aspartic Acid and Application of a Fluoride-Promoted S N Ar Coupling

Organic process research & development, 2011-11, Vol.15 (6), p.1328-1335

2011

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

Chemical communications (Cambridge, England), 2002-08 (15), p.1644-1645

2002

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Synthesis of Filibuvir. Part I. Diastereoselective Preparation of a β-Hydroxy Alkynyl Oxazolidinone and Conversion to a 6,6-Disubstituted 2 H -Pyranone

Organic process research & development, 2014-01, Vol.18 (1), p.26-35

2014

Volltextzugriff (PDF)

Synthesis of Filibuvir. Part II. Second-Generation Synthesis of a 6,6-Disubstituted 2 H -Pyranone via Dieckmann Cyclization of a β-Acetoxy Ester

Organic process research & development, 2014-01, Vol.18 (1), p.36-44

2014

Volltextzugriff (PDF)

OXIDATION OF PRIMARY ALCOHOLS TO CARBOXYLIC ACIDS WITH SODIUM CHLORITE CATALYZED BY TEMPO AND BLEACH: 4-METHOXYPHENYLACETIC ACID

Organic syntheses, 2005, Vol.81, p.195

2005

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Construction of the (1α,5α,6α)-6-Amino-3-azabicyclo[3.1.0]hexane Ring System

Synlett, 1996-11, Vol.1996 (11), p.1100-1102

1996

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ChemInform Abstract: Streamlined Synthesis of the Bippyphos Family of Ligands and Cross-Coupling Applications

ChemInform, 2008-09, Vol.39 (40), p.no-no

2008

Volltextzugriff (PDF)

Development of Nonproprietary Phosphine Ligands for the Pd-Catalyzed Amination Reaction

ChemInform, 2006-09, Vol.37 (37), p.no-no

2006

Volltextzugriff (PDF)

Cu-Catalyzed N-Arylation of Oxazolidinones: An Efficient Synthesis of the ϰ-Opioid Receptor Agonist CJ-15161 (I)

ChemInform, 2006-06, Vol.37 (25), p.no-no

2006

Volltextzugriff (PDF)

Development of Migita Couplings for the Manufacture of a 5-Lipoxygenase Inhibitor

Transition Metal-Catalyzed Couplings in Process Chemistry, 2013, p.253-266

2013

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Pharmacology, Medicinal Chemistry, Vaccines, Serums
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Streamlined Synthesis of the Bippyphos Family of Ligands and Cross-Coupling Applications

Development of an Efficient Pd-Catalyzed Coupling Process for Axitinib

Development of nonproprietary phosphine ligands for the Pd-catalyzed amination reaction

Ir-Catalyzed Borylation as an Efficient Route to a Nicotine Hapten

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

Blei

Palladium-Catalyzed Synthesis of N-Aryloxazolidinones from Aryl Chlorides

Development of the Commercial Route for the Manufacture of a 5‑Lipoxygenase Inhibitor PF-04191834

Synthesis of Filibuvir. Part I. Diastereoselective Preparation of a β‑Hydroxy Alkynyl Oxazolidinone and Conversion to a 6,6-Disubstituted 2H‑Pyranone

Cu-Catalyzed N-Arylation of Oxazolidinones: An Efficient Synthesis of the κ-Opioid Receptor Agonist CJ-15161

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

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

Synthesis of Filibuvir. Part II. Second-Generation Synthesis of a 6,6-Disubstituted 2H‑Pyranone via Dieckmann Cyclization of a β‑Acetoxy Ester

Cu-catalyzed N-arylation of oxazolidinones : An efficient synthesis of the k-opioid receptor agonist CJ-15161

Synthesis of a Bicyclic Piperazine from l-Aspartic Acid and Application of a Fluoride-Promoted SNAr Coupling

Synthesis of a Bicyclic Piperazine from l -Aspartic Acid and Application of a Fluoride-Promoted S N Ar Coupling

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

Synthesis of Filibuvir. Part I. Diastereoselective Preparation of a β-Hydroxy Alkynyl Oxazolidinone and Conversion to a 6,6-Disubstituted 2 H -Pyranone

Synthesis of Filibuvir. Part II. Second-Generation Synthesis of a 6,6-Disubstituted 2 H -Pyranone via Dieckmann Cyclization of a β-Acetoxy Ester

OXIDATION OF PRIMARY ALCOHOLS TO CARBOXYLIC ACIDS WITH SODIUM CHLORITE CATALYZED BY TEMPO AND BLEACH: 4-METHOXYPHENYLACETIC ACID

Construction of the (1α,5α,6α)-6-Amino-3-azabicyclo[3.1.0]hexane Ring System

ChemInform Abstract: Streamlined Synthesis of the Bippyphos Family of Ligands and Cross-Coupling Applications

Development of Nonproprietary Phosphine Ligands for the Pd-Catalyzed Amination Reaction

Cu-Catalyzed N-Arylation of Oxazolidinones: An Efficient Synthesis of the ϰ-Opioid Receptor Agonist CJ-15161 (I)

Development of Migita Couplings for the Manufacture of a 5-Lipoxygenase Inhibitor

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