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Metal-Catalyzed Ionic Decarboxylative Cross-Coupling Reactions of C(sp3) Acids: Reaction Development, Mechanisms, and Application

ACS catalysis, 2020-02, Vol.10 (3), p.1742-1753

2020

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Direct reversible decarboxylation from stable organic acids in dimethylformamide solution

Science (American Association for the Advancement of Science), 2020-07, Vol.369 (6503), p.557-561

2020

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Direct Catalytic Enantioselective Benzylation from Aryl Acetic Acids

Journal of the American Chemical Society, 2018-12, Vol.140 (50), p.17418-17422

2018

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Ambient Decarboxylative Arylation of Malonate Half-Esters via Oxidative Catalysis

Journal of the American Chemical Society, 2016-10, Vol.138 (42), p.13826-13829

2016

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Decarboxylative Benzylation of Aryl and Alkenyl Boronic Esters

Angewandte Chemie (International ed.), 2018-04, Vol.57 (17), p.4612-4616

International ed. in English, 2018

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Expanding the limit of Pd-catalyzed decarboxylative benzylations

Chemical communications (Cambridge, England), 2018, Vol.54 (50), p.6835-6838

2018

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Direct Catalytic Decarboxylative Amination of Aryl Acetic Acids

Angewandte Chemie (International ed.), 2020-01, Vol.59 (3), p.1313-1319

International ed. in English, 2020

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Synthesis and Reactivity of Unsymmetrical Azomethine Imines Formed Using Alkene Aminocarbonylation

Organic letters, 2013-04, Vol.15 (8), p.1890-1893

2013

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Intermolecular Aminocarbonylation of Alkenes using Concerted Cycloadditions of Iminoisocyanates

Journal of organic chemistry, 2017-01, Vol.82 (2), p.1175-1194

2017

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Organoboron-Catalyzed Regio- and Stereoselective Formation of β‑2-Deoxyglycosidic Linkages

Organic letters, 2014-07, Vol.16 (13), p.3604-3607

2014

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Oxidative Coupling of Aryl Boron Reagents with sp(3)-Carbon Nucleophiles: The Enolate Chan-Evans-Lam Reaction

Angewandte Chemie International Edition, 2016-01, Vol.55 (5), p.1894-1898

2016

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Oxidative cyclization reagents reveal tryptophan cation-π interactions

Nature (London), 2024-03, Vol.627 (8004), p.680-3

2024

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An Activity-Based Oxaziridine Platform for Identifying and Developing Covalent Ligands for Functional Allosteric Methionine Sites: Redox-Dependent Inhibition of Cyclin-Dependent Kinase 4

Journal of the American Chemical Society, 2022-12, Vol.144 (50), p.22890-22901

2022

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Kinetic Resolution of Azomethine Imines by Brønsted Acid Catalyzed Enantioselective Reduction

Angewandte Chemie (International ed.), 2015-12, Vol.54 (51), p.15516-15519

International ed. in English, 2015

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Z -Selective iridium-catalyzed cross-coupling of allylic carbonates and α-diazo esters

Chemical science (Cambridge), 2018-01, Vol.9 (1), p.238-244

2018

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Oxidative Coupling of Aryl Boron Reagents with sp3-Carbon Nucleophiles: The Enolate Chan-Evans-Lam Reaction

Angewandte Chemie (International ed.), 2016-01, Vol.55 (5), p.1894-1898

International ed. in English, 2016

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Direct Catalytic Decarboxylative Amination of Aryl Acetic Acids

Angewandte Chemie, 2020-01, Vol.132 (3), p.1329-1335

2020

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Decarboxylative Benzylation of Aryl and Alkenyl Boronic Esters

Angewandte Chemie, 2018-04, Vol.130 (17), p.4702-4706

2018

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Kinetic Resolution of Azomethine Imines by Brønsted Acid Catalyzed Enantioselective Reduction

Angewandte Chemie, 2015-12, Vol.127 (51), p.15736-15739

2015

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Oxidative Coupling of Aryl Boron Reagents with sp3-Carbon Nucleophiles: The Enolate Chan-Evans-Lam Reaction

Angewandte Chemie, 2016-01, Vol.128 (5), p.1926-1930

2016

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Expanding the limit of Pd-catalyzed decarboxylative benzylationsElectronic supplementary information (ESI) available: Synthetic procedures and characterization data. See DOI: 10.1039/c8cc02380h

2018-06

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Oxidative Coupling of Aryl Boron Reagents with sp 3 ‐Carbon Nucleophiles: The Enolate Chan–Evans–Lam Reaction

Angewandte Chemie International Edition, 2016-01, Vol.55 (5), p.1894-1898

2016

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Z-Selective iridium-catalyzed cross-coupling of allylic carbonates and α-diazo estersElectronic supplementary information (ESI) available: Full procedures, computational details and characterization data. See DOI: 10.1039/c7sc04283c

2017-12

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Z-Selective iridium-catalyzed cross-coupling of allylic carbonates and α-diazo esters† †Electronic supplementary information (ESI) available: Full procedures, computational details and characterization data. See DOI: 10.1039/c7sc04283c

Chemical science (Cambridge), 2017-10, Vol.9 (1), p.238-244

2017

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ChemInform Abstract: Kinetic Resolution of Azomethine Imines by Broensted Acid Catalyzed Enantioselective Reduction

ChemInform, 2016-03, Vol.47 (16), p.no-no

2016

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Metal-Catalyzed Ionic Decarboxylative Cross-Coupling Reactions of C(sp3) Acids: Reaction Development, Mechanisms, and Application

Direct reversible decarboxylation from stable organic acids in dimethylformamide solution

Direct Catalytic Enantioselective Benzylation from Aryl Acetic Acids

Ambient Decarboxylative Arylation of Malonate Half-Esters via Oxidative Catalysis

Decarboxylative Benzylation of Aryl and Alkenyl Boronic Esters

Expanding the limit of Pd-catalyzed decarboxylative benzylations

Direct Catalytic Decarboxylative Amination of Aryl Acetic Acids

Synthesis and Reactivity of Unsymmetrical Azomethine Imines Formed Using Alkene Aminocarbonylation

Intermolecular Aminocarbonylation of Alkenes using Concerted Cycloadditions of Iminoisocyanates

Organoboron-Catalyzed Regio- and Stereoselective Formation of β‑2-Deoxyglycosidic Linkages

Oxidative Coupling of Aryl Boron Reagents with sp(3)-Carbon Nucleophiles: The Enolate Chan-Evans-Lam Reaction

Oxidative cyclization reagents reveal tryptophan cation-π interactions

An Activity-Based Oxaziridine Platform for Identifying and Developing Covalent Ligands for Functional Allosteric Methionine Sites: Redox-Dependent Inhibition of Cyclin-Dependent Kinase 4

Kinetic Resolution of Azomethine Imines by Brønsted Acid Catalyzed Enantioselective Reduction

Z -Selective iridium-catalyzed cross-coupling of allylic carbonates and α-diazo esters

Oxidative Coupling of Aryl Boron Reagents with sp3-Carbon Nucleophiles: The Enolate Chan-Evans-Lam Reaction

Direct Catalytic Decarboxylative Amination of Aryl Acetic Acids

Decarboxylative Benzylation of Aryl and Alkenyl Boronic Esters

Kinetic Resolution of Azomethine Imines by Brønsted Acid Catalyzed Enantioselective Reduction

Oxidative Coupling of Aryl Boron Reagents with sp3-Carbon Nucleophiles: The Enolate Chan-Evans-Lam Reaction

Expanding the limit of Pd-catalyzed decarboxylative benzylationsElectronic supplementary information (ESI) available: Synthetic procedures and characterization data. See DOI: 10.1039/c8cc02380h

Oxidative Coupling of Aryl Boron Reagents with sp 3 ‐Carbon Nucleophiles: The Enolate Chan–Evans–Lam Reaction

Z-Selective iridium-catalyzed cross-coupling of allylic carbonates and α-diazo estersElectronic supplementary information (ESI) available: Full procedures, computational details and characterization data. See DOI: 10.1039/c7sc04283c

Z-Selective iridium-catalyzed cross-coupling of allylic carbonates and α-diazo esters† †Electronic supplementary information (ESI) available: Full procedures, computational details and characterization data. See DOI: 10.1039/c7sc04283c

ChemInform Abstract: Kinetic Resolution of Azomethine Imines by Broensted Acid Catalyzed Enantioselective Reduction

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