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Direct Acylation of C(sp3)−H Bonds Enabled by Nickel and Photoredox Catalysis

Angewandte Chemie (International ed.), 2016-03, Vol.55 (12), p.4040-4043

International ed. in English, 2016

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Development of a Platform for Near-Infrared Photoredox Catalysis

ACS central science, 2020-11, Vol.6 (11), p.2053-2059

2020

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Application of a Chiral Scaffolding Ligand in Catalytic Enantioselective Hydroformylation

Journal of the American Chemical Society, 2010-10, Vol.132 (42), p.14757-14759

2010

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Silicon Nanowires as Photoelectrodes for Carbon Dioxide Fixation

Angewandte Chemie (International ed.), 2012-07, Vol.51 (27), p.6709-6712

2012

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Ligand-Enabled β‑C(sp3)–H Olefination of Free Carboxylic Acids

Journal of the American Chemical Society, 2018-08, Vol.140 (32), p.10363-10367

2018

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Overcoming Photochemical Limitations in Metallaphotoredox Catalysis: Red-Light-Driven C–N Cross-Coupling

Journal of the American Chemical Society, 2022-12, Vol.144 (49), p.22409-22415

2022

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Ligand‐Enabled β‐C–H Arylation of α‐Amino Acids Without Installing Exogenous Directing Groups

Angewandte Chemie (International ed.), 2017-02, Vol.56 (6), p.1506-1509

2017

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Orange Light-Driven C(sp2)–C(sp3) Cross-Coupling via Spin-Forbidden Ir(III) Metallaphotoredox Catalysis

Journal of the American Chemical Society, 2023-09, Vol.145 (36), p.19925-19931

2023

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Catalytic α-Hydroarylation of Acrylates and Acrylamides via an Interrupted Hydrodehalogenation Reaction

Journal of the American Chemical Society, 2020-06, Vol.142 (23), p.10477-10484

2020

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Direct Acylation of C(sp3)−H Bonds Enabled by Nickel and Photoredox Catalysis

Angewandte Chemie, 2016-03, Vol.128 (12), p.4108-4111

2016

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Distal-Selective Hydroformylation using Scaffolding Catalysis

Journal of the American Chemical Society, 2014-06, Vol.136 (24), p.8556-8559

2014

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Coupling-Condensation Strategy for the Convergent Synthesis of an Imidazole-Fused 2‑Aminoquinoline NLRP3 Agonist

Journal of organic chemistry, 2023-01, Vol.88 (1), p.384-394

2023

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Ru-Catalyzed Enantioselective Hydrogenation of 2‑Pyridyl-Substituted Alkenes and Substrate-Mediated H/D Exchange

ACS catalysis, 2022-01, Vol.12 (2), p.1150-1160

2022

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Enantioselective Hydroformylation of Aniline Derivatives

Journal of organic chemistry, 2011-09, Vol.76 (18), p.7590-7596

2011

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Kinetic and Thermodynamic Considerations in the Rh-Catalyzed Enantioselective Hydrogenation of 2‑Pyridyl-Substituted Alkenes

ACS catalysis, 2022-05, Vol.12 (10), p.5961-5969

2022

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Development of a Scalable Synthetic Route to BMS-986251. Part 1: Synthesis of the Cyclohexane Dicarboxylate Fragment

Organic process research & development, 2021-07, Vol.25 (7), p.1547-1555

2021

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Red-Shifting Blue Light Photoredox Catalysis for Organic Synthesis: A Graphical Review

SynOpen (2017), 2023-02, Vol.7 (1), p.76-87

2023

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NMR Determination of Hydrogen Bond Thermodynamics in a Simple Diamide: A Physical Chemistry Experiment

Journal of chemical education, 2015-06, Vol.92 (6), p.1086-1090

2015

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Silicon Nanowires as Photoelectrodes for Carbon Dioxide Fixation

Angewandte Chemie, 2012-07, Vol.124 (27), p.6813-6816

2012

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Titelbild: Silicon Nanowires as Photoelectrodes for Carbon Dioxide Fixation (Angew. Chem. 27/2012)

Angewandte Chemie, 2012-07, Vol.124 (27), p.6641-6641

2012

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Ligand‐Enabled β‐C–H Arylation of α‐Amino Acids Without Installing Exogenous Directing Groups

Angewandte Chemie, 2017-02, Vol.129 (6), p.1528-1531

2017

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A Process Chemistry Benchmark for sp 2 –sp 3 Cross Couplings

Journal of organic chemistry, 2021-08, Vol.86 (15), p.10380-10396

2021

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A Process Chemistry Benchmark for sp2–sp3 Cross Couplings

Journal of organic chemistry, 2021-08, Vol.86 (15), p.10380-10396

2021

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Development of a Scalable Negishi Cross-Coupling Process for the Preparation of 2-Chloro-5-(1-(tetrahydro-2 H -pyran-2-yl)-1 H -pyrazol-5-yl)aniline

Organic process research & development, 2021-03, Vol.25 (3), p.434-441

2021

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Development of a Scalable Negishi Cross-Coupling Process for the Preparation of 2‑Chloro-5-(1-(tetrahydro‑2H‑pyran-2-yl)‑1H‑pyrazol-5-yl)aniline

Organic process research & development, 2021-03, Vol.25 (3), p.434-441

2021

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Direct Acylation of C(sp3)−H Bonds Enabled by Nickel and Photoredox Catalysis

Development of a Platform for Near-Infrared Photoredox Catalysis

Application of a Chiral Scaffolding Ligand in Catalytic Enantioselective Hydroformylation

Silicon Nanowires as Photoelectrodes for Carbon Dioxide Fixation

Ligand-Enabled β‑C(sp3)–H Olefination of Free Carboxylic Acids

Overcoming Photochemical Limitations in Metallaphotoredox Catalysis: Red-Light-Driven C–N Cross-Coupling

Ligand‐Enabled β‐C–H Arylation of α‐Amino Acids Without Installing Exogenous Directing Groups

Orange Light-Driven C(sp2)–C(sp3) Cross-Coupling via Spin-Forbidden Ir(III) Metallaphotoredox Catalysis

Catalytic α-Hydroarylation of Acrylates and Acrylamides via an Interrupted Hydrodehalogenation Reaction

Direct Acylation of C(sp3)−H Bonds Enabled by Nickel and Photoredox Catalysis

Distal-Selective Hydroformylation using Scaffolding Catalysis

Coupling-Condensation Strategy for the Convergent Synthesis of an Imidazole-Fused 2‑Aminoquinoline NLRP3 Agonist

Ru-Catalyzed Enantioselective Hydrogenation of 2‑Pyridyl-Substituted Alkenes and Substrate-Mediated H/D Exchange

Enantioselective Hydroformylation of Aniline Derivatives

Kinetic and Thermodynamic Considerations in the Rh-Catalyzed Enantioselective Hydrogenation of 2‑Pyridyl-Substituted Alkenes

Development of a Scalable Synthetic Route to BMS-986251. Part 1: Synthesis of the Cyclohexane Dicarboxylate Fragment

Red-Shifting Blue Light Photoredox Catalysis for Organic Synthesis: A Graphical Review

NMR Determination of Hydrogen Bond Thermodynamics in a Simple Diamide: A Physical Chemistry Experiment

Silicon Nanowires as Photoelectrodes for Carbon Dioxide Fixation

Titelbild: Silicon Nanowires as Photoelectrodes for Carbon Dioxide Fixation (Angew. Chem. 27/2012)

Ligand‐Enabled β‐C–H Arylation of α‐Amino Acids Without Installing Exogenous Directing Groups

A Process Chemistry Benchmark for sp 2 –sp 3 Cross Couplings

A Process Chemistry Benchmark for sp2–sp3 Cross Couplings

Development of a Scalable Negishi Cross-Coupling Process for the Preparation of 2-Chloro-5-(1-(tetrahydro-2 H -pyran-2-yl)-1 H -pyrazol-5-yl)aniline

Development of a Scalable Negishi Cross-Coupling Process for the Preparation of 2‑Chloro-5-(1-(tetrahydro‑2H‑pyran-2-yl)‑1H‑pyrazol-5-yl)aniline

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