Works matching AU Lewis, Jared C.
Results: 32
Selective C−H Halogenation of Alkenes and Alkynes Using Flavin‐Dependent Halogenases.
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- Angewandte Chemie, 2024, v. 136, n. 13, p. 1, doi. 10.1002/ange.202317860
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- Article
Non‐native Intramolecular Radical Cyclization Catalyzed by a B<sub>12</sub>‐Dependent Enzyme.
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- Angewandte Chemie, 2023, v. 135, n. 51, p. 1, doi. 10.1002/ange.202312893
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Directed Evolution of an Iron(II)‐ and α‐Ketoglutarate‐Dependent Dioxygenase for Site‐Selective Azidation of Unactivated Aliphatic C−H Bonds**.
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- Angewandte Chemie, 2023, v. 135, n. 15, p. 1, doi. 10.1002/ange.202301370
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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.
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- Angewandte Chemie, 2022, v. 134, n. 51, p. 1, doi. 10.1002/ange.202214610
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- Article
Frontispiz: Engineering Dirhodium Artificial Metalloenzymes for Diazo Coupling Cascade Reactions.
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- Angewandte Chemie, 2021, v. 133, n. 44, p. 1, doi. 10.1002/ange.202184462
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Engineering Dirhodium Artificial Metalloenzymes for Diazo Coupling Cascade Reactions**.
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- Angewandte Chemie, 2021, v. 133, n. 44, p. 23865, doi. 10.1002/ange.202107982
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Catalytic Behavior of Mono‐N‐Protected Amino‐Acid Ligands in Ligand‐Accelerated C−H Activation by Palladium(II).
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- Angewandte Chemie, 2020, v. 132, n. 27, p. 10965, doi. 10.1002/ange.202002484
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Aromatic Halogenation by Using Bifunctional Flavin Reductase-Halogenase Fusion Enzymes.
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- ChemBioChem, 2017, v. 18, n. 21, p. 2099, doi. 10.1002/cbic.201700391
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Asymmetric catalysis by flavin‐dependent halogenases.
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- Chirality, 2023, v. 35, n. 8, p. 452, doi. 10.1002/chir.23550
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Preparation, Characterization, and Oxygenase Activity of a Photocatalytic Artificial Enzyme.
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- ChemBioChem, 2015, v. 16, n. 13, p. 1880, doi. 10.1002/cbic.201500165
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Improving the Stability and Catalyst Lifetime of the Halogenase RebH By Directed Evolution.
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- ChemBioChem, 2014, v. 15, n. 9, p. 1286, doi. 10.1002/cbic.201300780
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Cover Picture: A General Method for Artificial Metalloenzyme Formation through Strain-Promoted Azide-Alkyne Cycloaddition (ChemBioChem 2/2014).
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- ChemBioChem, 2014, v. 15, n. 2, p. 173, doi. 10.1002/cbic.201490000
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A General Method for Artificial Metalloenzyme Formation through Strain-Promoted Azide-Alkyne Cycloaddition.
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- ChemBioChem, 2014, v. 15, n. 2, p. 223, doi. 10.1002/cbic.201300661
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Combinatorial Alanine Substitution Enables Rapid Optimization of Cytochrome P450<sub>BM3</sub> for Selective Hydroxylation of Large Substrates.
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- ChemBioChem, 2010, v. 11, n. 18, p. 2502, doi. 10.1002/cbic.201000565
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Metal-responsive regulation of enzyme catalysis using genetically encoded chemical switches.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-29239-y
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- Article
Selective C−H Halogenation of Alkenes and Alkynes Using Flavin‐Dependent Halogenases.
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- Angewandte Chemie International Edition, 2024, v. 63, n. 13, p. 1, doi. 10.1002/anie.202317860
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- Article
Engineering a dirhodium artificial metalloenzyme for selective olefin cyclopropanation.
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- Nature Communications, 2015, v. 6, n. 7, p. 7789, doi. 10.1038/ncomms8789
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- Article
Non‐native Intramolecular Radical Cyclization Catalyzed by a B<sub>12</sub>‐Dependent Enzyme.
- Published in:
- Angewandte Chemie International Edition, 2023, v. 62, n. 51, p. 1, doi. 10.1002/anie.202312893
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- Publication type:
- Article
Directed Evolution of an Iron(II)‐ and α‐Ketoglutarate‐Dependent Dioxygenase for Site‐Selective Azidation of Unactivated Aliphatic C−H Bonds**.
- Published in:
- Angewandte Chemie International Edition, 2023, v. 62, n. 15, p. 1, doi. 10.1002/anie.202301370
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- Publication type:
- Article
The Single‐Component Flavin Reductase/Flavin‐Dependent Halogenase AetF is a Versatile Catalyst for Selective Bromination and Iodination of Arenes and Olefins.
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- Angewandte Chemie International Edition, 2022, v. 61, n. 51, p. 1, doi. 10.1002/anie.202214610
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- Publication type:
- Article
Frontispiece: Engineering Dirhodium Artificial Metalloenzymes for Diazo Coupling Cascade Reactions.
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- Angewandte Chemie International Edition, 2021, v. 60, n. 44, p. 1, doi. 10.1002/anie.202184462
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- Article
Engineering Dirhodium Artificial Metalloenzymes for Diazo Coupling Cascade Reactions**.
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- Angewandte Chemie International Edition, 2021, v. 60, n. 44, p. 23672, doi. 10.1002/anie.202107982
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- Article
Catalytic Behavior of Mono‐N‐Protected Amino‐Acid Ligands in Ligand‐Accelerated C−H Activation by Palladium(II).
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- Angewandte Chemie International Edition, 2020, v. 59, n. 27, p. 10873, doi. 10.1002/anie.202002484
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- Article
Microwave-Promoted Rhodium-Catalyzed Arylation of Heterocycles through C—H Bond ActivationThis work was supported by the NIH (grant no. GM069559, to J.A.E.) and by the Director, Office of Energy Research, Office of Basic Energy Sciences, Chemical Sciences Division, US Department of Energy (contract no. DE-AC03-76SF00098, to R.G.B.). J.Y.W. is funded by the Jean Dreyfus Boissevain Award. We gratefully acknowledge Dr. Fredrick J. Hollander and Dr. Allen G. Oliver at the UCB X-ray diffraction facility (CHEXRAY) for solving the structures of 4 a and 4 b, and Jeffrey McMahon for many helpful discussions. Dr. Wolfgang Meyer of Sasol Corp. is acknowledged for helpful advice on phobane alkylation.
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- Angewandte Chemie, 2006, v. 118, n. 10, p. 1619, doi. 10.1002/ange.200504289
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- Article
Directed Evolution of RebH for Site-Selective Halogenation of Large Biologically Active Molecules.
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- Angewandte Chemie, 2015, v. 127, n. 14, p. 4300, doi. 10.1002/ange.201411901
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Enantioselective Intramolecular CH Amination Catalyzed by Engineered Cytochrome P450 Enzymes In Vitro and In Vivo.
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- Angewandte Chemie, 2013, v. 125, n. 35, p. 9479, doi. 10.1002/ange.201304401
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Regioselective Arene Halogenation using the FAD-Dependent Halogenase RebH.
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- Angewandte Chemie, 2013, v. 125, n. 20, p. 5379, doi. 10.1002/ange.201300762
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- Article
Microwave-Promoted Rhodium-Catalyzed Arylation of Heterocycles through C—H Bond ActivationThis work was supported by the NIH (grant no. GM069559, to J.A.E.) and by the Director, Office of Energy Research, Office of Basic Energy Sciences, Chemical Sciences Division, US Department of Energy (contract no. DE-AC03-76SF00098, to R.G.B.). J.Y.W. is funded by the Jean Dreyfus Boissevain Award. We gratefully acknowledge Dr. Fredrick J. Hollander and Dr. Allen G. Oliver at the UCB X-ray diffraction facility (CHEXRAY) for solving the structures of 4 a and 4 b, and Jeffrey McMahon for many helpful discussions. Dr. Wolfgang Meyer of Sasol Corp. is acknowledged for helpful advice on phobane alkylation.
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- Angewandte Chemie International Edition, 2006, v. 45, n. 10, p. 1589, doi. 10.1002/anie.200504289
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- Article
Flavin-dependent halogenases catalyze enantioselective olefin halocyclization.
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- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-23503-3
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- Article
Directed Evolution of RebH for Site-Selective Halogenation of Large Biologically Active Molecules.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 14, p. 4226, doi. 10.1002/anie.201411901
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- Article
Enantioselective Intramolecular CH Amination Catalyzed by Engineered Cytochrome P450 Enzymes In Vitro and In Vivo.
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- Angewandte Chemie International Edition, 2013, v. 52, n. 35, p. 9309, doi. 10.1002/anie.201304401
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- Publication type:
- Article
Regioselective Arene Halogenation using the FAD-Dependent Halogenase RebH.
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- Angewandte Chemie International Edition, 2013, v. 52, n. 20, p. 5271, doi. 10.1002/anie.201300762
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- Publication type:
- Article