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Synthesis of Tri‐ and Difluoromethoxylated Compounds by Visible‐Light Photoredox Catalysis

Angewandte Chemie International Edition, 2019-08, Vol.58 (33), p.11171-11181

International ed. in English, 2019

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Redox‐Neutral TEMPO Catalysis: Direct Radical (Hetero)Aryl C−H Di‐ and Trifluoromethoxylation

Angewandte Chemie International Edition, 2020-11, Vol.59 (48), p.21475-21480

International ed. in English, 2020

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Access to a new class of synthetic building blocks via trifluoromethoxylation of pyridines and pyrimidines

Chemical science (Cambridge), 2016-01, Vol.7 (1), p.424-429

2016

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Catalytic radical difluoromethoxylation of arenes and heteroarenes

Chemical science (Cambridge), 2019-03, Vol.10 (11), p.3217-3222

2019

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Development of the Commercial Manufacturing Process for Nirmatrelvir in 17 Months

ACS central science, 2023-05, Vol.9 (5), p.849-857

2023

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Recovery rheology via rheo‐SANS: Application to step strains under out‐of‐equilibrium conditions

AIChE journal, 2019-12, Vol.65 (12), p.n/a

2019

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Recent Development of Catalytic Trifluoromethoxylation Reactions

Tetrahedron, 2018-12, Vol.74 (50), p.7127-7135

2018

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Redox‐Active Reagents for Photocatalytic Generation of the OCF3 Radical and (Hetero)Aryl C−H Trifluoromethoxylation

Angewandte Chemie International Edition, 2018-10, Vol.57 (42), p.13795-13799

International ed. in English, 2018

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Catalytic C−H Trifluoromethoxylation of Arenes and Heteroarenes

Angewandte Chemie International Edition, 2018-07, Vol.57 (31), p.9645-9649

International ed. in English, 2018

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Synthesis of Tri‐ and Difluoromethoxylated Compounds by Visible‐Light Photoredox Catalysis

Angewandte Chemie, 2019-08, Vol.131 (33), p.11289-11299

2019

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Selective C-O bond formation via a photocatalytic radical coupling strategy: access to perfluoroalkoxylated (OR F ) arenes and heteroarenes

Chemical science (Cambridge), 2017-09, Vol.8 (9), p.6066-6070

2017

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Synthesis of Trifluoromethoxylated (Hetero)Arenes via OCF3 Migration

Synlett, 2015-11, Vol.27 (3), p.313-319

2015

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The Single‐Component Flavin Reductase/Flavin‐Dependent Halogenase AetF is a Versatile Catalyst for Selective Bromination and Iodination of Arenes and Olefins

Angewandte Chemie International Edition, 2022-12, Vol.61 (51), p.e202214610-n/a

International ed. in English, 2022

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Catalytic C−H Trifluoromethoxylation of Arenes and Heteroarenes

Angewandte Chemie, 2018-07, Vol.130 (31), p.9793-9797

2018

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Redox-Active Reagents for Photocatalytic Generation of the OCF 3 Radical and (Hetero)Aryl C-H Trifluoromethoxylation

Angewandte Chemie International Edition, 2018-10, Vol.57 (42), p.13795-13799

2018

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Transition-metal-free C-H amidation and chlorination: synthesis of N/N'-mono-substituted imidazopyridin-2-ones from N-pyridyl-N-hydroxylamine intermediates

Chemical communications (Cambridge, England), 2018-06, Vol.54 (50), p.6935-6938

2018

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Redox‐Neutral TEMPO Catalysis: Direct Radical (Hetero)Aryl C−H Di‐ and Trifluoromethoxylation

Angewandte Chemie, 2020-11, Vol.132 (48), p.21659-21664

2020

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The Single‐Component Flavin Reductase/Flavin‐Dependent Halogenase AetF is a Versatile Catalyst for Selective Bromination and Iodination of Arenes and Olefins

Angewandte Chemie, 2022-12, Vol.134 (51), p.n/a

2022

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Redox‐Active Reagents for Photocatalytic Generation of the OCF3 Radical and (Hetero)Aryl C−H Trifluoromethoxylation

Angewandte Chemie, 2018-10, Vol.130 (42), p.13991-13995

2018

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Redox-Neutral TEMPO Catalysis Toward Direct Radical (Hetero)Aryl C–H Di- and Trifluoromethoxylation

Angewandte Chemie International Edition, 2020-09, Vol.59 (48), p.21475-21480

2020

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Sustainable Manufacturing of trans-4-Trifluoromethyl‑l‑proline via Stereochemical Editing: A Combined In Silico and Experimental Approach

Organic process research & development, 2024-10, Vol.28 (10), p.3827-3836

2024

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Transition-metal-free C-H amidation and chlorination: synthesis of N/N′-mono-substituted imidazopyridin-2-ones from N-pyridyl-N-hydroxylamine intermediatesElectronic supplementary information (ESI) available. See DOI: 10.1039/c8cc02425a

2018-06

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Selective C-O bond formation via a photocatalytic radical coupling strategy: access to perfluoroalkoxylated (ORF) arenes and heteroarenesElectronic supplementary information (ESI) available. See DOI: 10.1039/c7sc01684k

2017-08

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Selective C–O bond formation via a photocatalytic radical coupling strategy: access to perfluoroalkoxylated (ORF) arenes and heteroarenes† †Electronic supplementary information (ESI) available. See DOI: 10.1039/c7sc01684k Click here for additional data file

Chemical science (Cambridge), 2017-06, Vol.8 (9), p.6066-6070

2017

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Synthesis of Nirmatrelvir: Design and Optimization of an Efficient Telescoped Amidation–Dehydration Sequence

Organic process research & development, 2023-12, Vol.27 (12), p.2250-2259

2023

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Synthesis of Tri‐ and Difluoromethoxylated Compounds by Visible‐Light Photoredox Catalysis

Redox‐Neutral TEMPO Catalysis: Direct Radical (Hetero)Aryl C−H Di‐ and Trifluoromethoxylation

Access to a new class of synthetic building blocks via trifluoromethoxylation of pyridines and pyrimidines

Catalytic radical difluoromethoxylation of arenes and heteroarenes

Development of the Commercial Manufacturing Process for Nirmatrelvir in 17 Months

Recovery rheology via rheo‐SANS: Application to step strains under out‐of‐equilibrium conditions

Recent Development of Catalytic Trifluoromethoxylation Reactions

Redox‐Active Reagents for Photocatalytic Generation of the OCF3 Radical and (Hetero)Aryl C−H Trifluoromethoxylation

Catalytic C−H Trifluoromethoxylation of Arenes and Heteroarenes

Synthesis of Tri‐ and Difluoromethoxylated Compounds by Visible‐Light Photoredox Catalysis

Selective C-O bond formation via a photocatalytic radical coupling strategy: access to perfluoroalkoxylated (OR F ) arenes and heteroarenes

Synthesis of Trifluoromethoxylated (Hetero)Arenes via OCF3 Migration

The Single‐Component Flavin Reductase/Flavin‐Dependent Halogenase AetF is a Versatile Catalyst for Selective Bromination and Iodination of Arenes and Olefins

Catalytic C−H Trifluoromethoxylation of Arenes and Heteroarenes

Redox-Active Reagents for Photocatalytic Generation of the OCF 3 Radical and (Hetero)Aryl C-H Trifluoromethoxylation

Transition-metal-free C-H amidation and chlorination: synthesis of N/N'-mono-substituted imidazopyridin-2-ones from N-pyridyl-N-hydroxylamine intermediates

Redox‐Neutral TEMPO Catalysis: Direct Radical (Hetero)Aryl C−H Di‐ and Trifluoromethoxylation

The Single‐Component Flavin Reductase/Flavin‐Dependent Halogenase AetF is a Versatile Catalyst for Selective Bromination and Iodination of Arenes and Olefins

Redox‐Active Reagents for Photocatalytic Generation of the OCF3 Radical and (Hetero)Aryl C−H Trifluoromethoxylation

Redox-Neutral TEMPO Catalysis Toward Direct Radical (Hetero)Aryl C–H Di- and Trifluoromethoxylation

Sustainable Manufacturing of trans-4-Trifluoromethyl‑l‑proline via Stereochemical Editing: A Combined In Silico and Experimental Approach

Transition-metal-free C-H amidation and chlorination: synthesis of N/N′-mono-substituted imidazopyridin-2-ones from N-pyridyl-N-hydroxylamine intermediatesElectronic supplementary information (ESI) available. See DOI: 10.1039/c8cc02425a

Selective C-O bond formation via a photocatalytic radical coupling strategy: access to perfluoroalkoxylated (ORF) arenes and heteroarenesElectronic supplementary information (ESI) available. See DOI: 10.1039/c7sc01684k

Selective C–O bond formation via a photocatalytic radical coupling strategy: access to perfluoroalkoxylated (ORF) arenes and heteroarenes† †Electronic supplementary information (ESI) available. See DOI: 10.1039/c7sc01684k Click here for additional data file

Synthesis of Nirmatrelvir: Design and Optimization of an Efficient Telescoped Amidation–Dehydration Sequence

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