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Ligand-controlled divergent dehydrogenative reactions of carboxylic acids via C-H activation

Science (American Association for the Advancement of Science), 2021-12, Vol.374 (6572), p.1281-1285

2021

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Palladium(II)‐Catalyzed Site‐Selective C(sp3)−H Alkynylation of Oligopeptides: A Linchpin Approach for Oligopeptide–Drug Conjugation

Angewandte Chemie (International ed.), 2017-08, Vol.56 (36), p.10924-10927

International ed. in English, 2017

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Decarboxylative alkylation for site-selective bioconjugation of native proteins via oxidation potentials

Nature chemistry, 2018-02, Vol.10 (2), p.205

2018

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Ligand-accelerated non-directed C-H functionalization of arenes

Nature (London), 2017-11, Vol.551 (7681), p.489-493

2017

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Site-Selective Functionalization of Methionine Residues via Photoredox Catalysis

Journal of the American Chemical Society, 2020-12, Vol.142 (51), p.21260-21266

2020

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meta C–H Arylation of Electron-Rich Arenes: Reversing the Conventional Site Selectivity

Journal of the American Chemical Society, 2019-09, Vol.141 (37), p.14870-14877

2019

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meta‐Selective C−H Arylation of Fluoroarenes and Simple Arenes

Angewandte Chemie (International ed.), 2020-08, Vol.59 (33), p.13831-13835

International ed. in English, 2020

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Decarboxylative Peptide Macrocyclization through Photoredox Catalysis

Angewandte Chemie (International ed.), 2017-01, Vol.56 (3), p.728-732

International ed. in English, 2017

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Ligand-Enabled Pd(II)-Catalyzed C(sp3)–H Lactonization Using Molecular Oxygen as Oxidant

Organic letters, 2020-05, Vol.22 (10), p.3960-3963

2020

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A General Amino Acid Synthesis Enabled by Innate Radical Cross‐Coupling

Angewandte Chemie (International ed.), 2018-10, Vol.57 (44), p.14560-14565

International ed. in English, 2018

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Remote C−H Olefination of Heterocyclic Biaryls Enabled by Reversibly Bound Templates

Angewandte Chemie (International ed.), 2023-09, Vol.62 (37), p.e202307581-n/a

International ed. in English, 2023

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PdII‐Catalyzed Enantioselective C(sp3)−H Activation/Cross‐Coupling Reactions of Free Carboxylic Acids

Angewandte Chemie (International ed.), 2019-02, Vol.58 (7), p.2134-2138

International ed. in English, 2019

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Overcoming the Limitations of γ- and δ‑C–H Arylation of Amines through Ligand Development

Journal of the American Chemical Society, 2018-12, Vol.140 (51), p.17884-17894

2018

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Ligand-Enabled C–H Hydroxylation with Aqueous H2O2 at Room Temperature

Journal of the American Chemical Society, 2022-10, Vol.144 (39), p.18109-18116

2022

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Pd II -Catalyzed Enantioselective C(sp 3 )-H Activation/Cross-Coupling Reactions of Free Carboxylic Acids

Angewandte Chemie International Edition, 2019-02, Vol.58 (7), p.2134-2138

2019

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Pd-Catalyzed γ-C(sp 3 )-H Fluorination of Free Amines

Journal of the American Chemical Society, 2020-06, Vol.142 (22), p.9966-9974

2020

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A tautomeric ligand enables directed C‒H hydroxylation with molecular oxygen

Science (American Association for the Advancement of Science), 2021-06, Vol.372 (6549), p.1452-1457

2021

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Transient Directing Group Enabled Pd-Catalyzed γ‑C(sp3)–H Oxygenation of Alkyl Amines

ACS catalysis, 2020-05, Vol.10 (10), p.5657-5662

2020

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AlMe3-Promoted Formation of Amides from Acids and Amines

Organic letters, 2012-01, Vol.14 (1), p.214-217

2012

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One-Step Synthesis of β‑Alkylidene-γ-lactones via Ligand-Enabled β,γ-Dehydrogenation of Aliphatic Acids

Journal of the American Chemical Society, 2022-07, Vol.144 (28), p.12924-12933

2022

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Synthesis of 1,3-Dienes via Ligand-Enabled Sequential Dehydrogenation of Aliphatic Acids

Journal of the American Chemical Society, 2023-06, Vol.145 (24), p.13003-13007

2023

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Iridium(I)-Catalyzed α‑C(sp3)–H Alkylation of Saturated Azacycles

Journal of the American Chemical Society, 2020-03, Vol.142 (11), p.5117-5125

2020

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Transformation of Anionically Activated Trifluoromethyl Groups to Heterocycles under Mild Aqueous Conditions

Organic letters, 2011-04, Vol.13 (7), p.1804-1807

2011

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Formation of α-chiral centers by asymmetric β-C(sp3)-H arylation, alkenylation, and alkynylation

Science (American Association for the Advancement of Science), 2017-02, Vol.355 (6324), p.499-503

2017

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Ligand-controlled divergent dehydrogenative reactions of carboxylic acids via C-H activation

Palladium(II)‐Catalyzed Site‐Selective C(sp3)−H Alkynylation of Oligopeptides: A Linchpin Approach for Oligopeptide–Drug Conjugation

Decarboxylative alkylation for site-selective bioconjugation of native proteins via oxidation potentials

Ligand-accelerated non-directed C-H functionalization of arenes

Site-Selective Functionalization of Methionine Residues via Photoredox Catalysis

meta C–H Arylation of Electron-Rich Arenes: Reversing the Conventional Site Selectivity

meta‐Selective C−H Arylation of Fluoroarenes and Simple Arenes

Decarboxylative Peptide Macrocyclization through Photoredox Catalysis

Ligand-Enabled Pd(II)-Catalyzed C(sp3)–H Lactonization Using Molecular Oxygen as Oxidant

A General Amino Acid Synthesis Enabled by Innate Radical Cross‐Coupling

Remote C−H Olefination of Heterocyclic Biaryls Enabled by Reversibly Bound Templates

PdII‐Catalyzed Enantioselective C(sp3)−H Activation/Cross‐Coupling Reactions of Free Carboxylic Acids

Overcoming the Limitations of γ- and δ‑C–H Arylation of Amines through Ligand Development

Ligand-Enabled C–H Hydroxylation with Aqueous H2O2 at Room Temperature

Pd II -Catalyzed Enantioselective C(sp 3 )-H Activation/Cross-Coupling Reactions of Free Carboxylic Acids

Pd-Catalyzed γ-C(sp 3 )-H Fluorination of Free Amines

Conformationally Constrained ortho-Anilino Diaryl Ureas: Discovery of 1‑(2-(1′-Neopentylspiro[indoline-3,4′-piperidine]-1-yl)phenyl)-3-(4-(trifluoromethoxy)phenyl)urea, a Potent, Selective, and Bioavailable P2Y1 Antagonist

A tautomeric ligand enables directed C‒H hydroxylation with molecular oxygen

Transient Directing Group Enabled Pd-Catalyzed γ‑C(sp3)–H Oxygenation of Alkyl Amines

AlMe3-Promoted Formation of Amides from Acids and Amines

One-Step Synthesis of β‑Alkylidene-γ-lactones via Ligand-Enabled β,γ-Dehydrogenation of Aliphatic Acids

Synthesis of 1,3-Dienes via Ligand-Enabled Sequential Dehydrogenation of Aliphatic Acids

Iridium(I)-Catalyzed α‑C(sp3)–H Alkylation of Saturated Azacycles

Transformation of Anionically Activated Trifluoromethyl Groups to Heterocycles under Mild Aqueous Conditions

Formation of α-chiral centers by asymmetric β-C(sp3)-H arylation, alkenylation, and alkynylation

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