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Monitoring chemical reactions by low-field benchtop NMR at 45 MHz: pros and cons

Magnetic resonance in chemistry, 2016-06, Vol.54 (6), p.437-443

2016

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SLC46A3 Is Required to Transport Catabolites of Noncleavable Antibody Maytansine Conjugates from the Lysosome to the Cytoplasm

Cancer research (Chicago, Ill.), 2015-12, Vol.75 (24), p.5329-5340

2015

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Monitoring chemical reactions by low-field benchtop NMR at 45MHz: pros and cons

Magnetic resonance in chemistry, 2016-06, Vol.54 (6), p.437-443

2016

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

Organic process research & development, 2015-12, Vol.19 (12), p.1849-1858

2015

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3,3‘-Dipyridyl BINOL Ligands. Synthesis and Application in Enantioselective Addition of Et2Zn to Aldehydes

Organic letters, 2007-10, Vol.9 (22), p.4403-4406

2007

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Altering Antibody–Drug Conjugate Binding to the Neonatal Fc Receptor Impacts Efficacy and Tolerability

Molecular pharmaceutics, 2016-07, Vol.13 (7), p.2387-2396

2016

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Application of In Situ Raman Spectroscopy To Facilitate Use of Hydrogen Peroxide on Kilogram Scale

Organic process research & development, 2014-12, Vol.18 (12), p.1807-1811

2014

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ortho-Anisylsulfonyl as a Protecting Group for Secondary Amines: Mild Ni0-Catalyzed Hydrodesulfonylation

Angewandte Chemie (International ed.), 2004-02, Vol.43 (7), p.892-894

2004

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Total Synthesis of Marinomycins A−C and of Their Monomeric Counterparts Monomarinomycin A and iso-Monomarinomycin A

Journal of the American Chemical Society, 2007-02, Vol.129 (6), p.1760-1768

2007

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Total Synthesis of Marinomycins A-C

Angewandte Chemie (International ed.), 2006-10, Vol.45 (39), p.6527-6532

2006

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Development of a Practical Synthesis of a Pyrazolopyridinone-Based p38 MAP Kinase Inhibitor

Organic process research & development, 2011-01, Vol.15 (1), p.31-43

2011

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Stereocontrolled Synthesis of Model Core Systems of Lomaiviticins A and B

Angewandte Chemie (International ed.), 2006-03, Vol.45 (13), p.2076-2081

2006

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Directed ortho Metalation Reaction of Aryl O-Carbamates on Solid Support

Organic letters, 2005-02, Vol.7 (4), p.629-631

2005

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The Tertiary Sulfonamide as a Latent Directed-Metalation Group: Ni0-Catalyzed Reductive Cleavage and Cross-Coupling Reactions of Aryl Sulfonamides with Grignard Reagents

Angewandte Chemie (International ed.), 2004-02, Vol.43 (7), p.888-891

2004

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The Tertiary Sulfonamide as a Latent Directed‐Metalation Group: Ni 0 ‐Catalyzed Reductive Cleavage and Cross‐Coupling Reactions of Aryl Sulfonamides with Grignard Reagents

Angewandte Chemie International Edition, 2004-02, Vol.43 (7), p.888-891

2004

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A practical preparation of aryl β-ketophosphonates

Tetrahedron letters, 2009-02, Vol.50 (8), p.870-872

2009

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ortho ‐Anisylsulfonyl as a Protecting Group for Secondary Amines: Mild Ni 0 ‐Catalyzed Hydrodesulfonylation

Angewandte Chemie International Edition, 2004-02, Vol.43 (7), p.892-894

2004

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ortho ‐Anisylsulfonyl as a Protecting Group for Secondary Amines: Mild Ni 0 ‐Catalyzed Hydrodesulfonylation

Angewandte Chemie, 2004-02, Vol.116 (7), p.910-912

2004

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3,3‘-Dipyridyl BINOL Ligands. Synthesis and Application in Enantioselective Addition of Et 2 Zn to Aldehydes

Organic letters, 2007-10, Vol.9 (22), p.4403-4406

2007

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Total Synthesis of Marinomycins A–C

Angewandte Chemie, 2006-10, Vol.118 (39), p.6677-6682

2006

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Stereocontrolled Synthesis of Model Core Systems of Lomaiviticins A and B

Angewandte Chemie, 2006-03, Vol.118 (13), p.2130-2135

2006

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The Tertiary Sulfonamide as a Latent Directed-Metalation Group: Ni0-Catalyzed Reductive Cleavage and Cross-Coupling Reactions of Aryl Sulfonamides with Grignard Reagents

Angewandte Chemie, 2004-02, Vol.116 (7), p.906-909

2004

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ortho-Anisylsulfonyl as a Protecting Group for Secondary Amines: Mild Ni0-Catalyzed Hydrodesulfonylation

Angewandte Chemie, 2004-02, Vol.116 (7), p.910-912

2004

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The Tertiary Sulfonamide as a Latent Directed‐Metalation Group: Ni 0 ‐Catalyzed Reductive Cleavage and Cross‐Coupling Reactions of Aryl Sulfonamides with Grignard Reagents

Angewandte Chemie, 2004-02, Vol.116 (7), p.906-909

2004

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Total Synthesis of Marinomycins A-C

Angewandte Chemie, 2006-10, Vol.118 (39), p.6677-6682

2006

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Monitoring chemical reactions by low-field benchtop NMR at 45 MHz: pros and cons

SLC46A3 Is Required to Transport Catabolites of Noncleavable Antibody Maytansine Conjugates from the Lysosome to the Cytoplasm

Monitoring chemical reactions by low-field benchtop NMR at 45MHz: pros and cons

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

3,3‘-Dipyridyl BINOL Ligands. Synthesis and Application in Enantioselective Addition of Et2Zn to Aldehydes

Altering Antibody–Drug Conjugate Binding to the Neonatal Fc Receptor Impacts Efficacy and Tolerability

Application of In Situ Raman Spectroscopy To Facilitate Use of Hydrogen Peroxide on Kilogram Scale

ortho-Anisylsulfonyl as a Protecting Group for Secondary Amines: Mild Ni0-Catalyzed Hydrodesulfonylation

Total Synthesis of Marinomycins A−C and of Their Monomeric Counterparts Monomarinomycin A and iso-Monomarinomycin A

Total Synthesis of Marinomycins A-C

Development of a Practical Synthesis of a Pyrazolopyridinone-Based p38 MAP Kinase Inhibitor

Stereocontrolled Synthesis of Model Core Systems of Lomaiviticins A and B

Directed ortho Metalation Reaction of Aryl O-Carbamates on Solid Support

The Tertiary Sulfonamide as a Latent Directed-Metalation Group: Ni0-Catalyzed Reductive Cleavage and Cross-Coupling Reactions of Aryl Sulfonamides with Grignard Reagents

The Tertiary Sulfonamide as a Latent Directed‐Metalation Group: Ni 0 ‐Catalyzed Reductive Cleavage and Cross‐Coupling Reactions of Aryl Sulfonamides with Grignard Reagents

A practical preparation of aryl β-ketophosphonates

ortho ‐Anisylsulfonyl as a Protecting Group for Secondary Amines: Mild Ni 0 ‐Catalyzed Hydrodesulfonylation

ortho ‐Anisylsulfonyl as a Protecting Group for Secondary Amines: Mild Ni 0 ‐Catalyzed Hydrodesulfonylation

3,3‘-Dipyridyl BINOL Ligands. Synthesis and Application in Enantioselective Addition of Et 2 Zn to Aldehydes

Total Synthesis of Marinomycins A–C

Stereocontrolled Synthesis of Model Core Systems of Lomaiviticins A and B

The Tertiary Sulfonamide as a Latent Directed-Metalation Group: Ni0-Catalyzed Reductive Cleavage and Cross-Coupling Reactions of Aryl Sulfonamides with Grignard Reagents

ortho-Anisylsulfonyl as a Protecting Group for Secondary Amines: Mild Ni0-Catalyzed Hydrodesulfonylation

The Tertiary Sulfonamide as a Latent Directed‐Metalation Group: Ni 0 ‐Catalyzed Reductive Cleavage and Cross‐Coupling Reactions of Aryl Sulfonamides with Grignard Reagents

Total Synthesis of Marinomycins A-C

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