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Advancing the Logic of Chemical Synthesis: C−H Activation as Strategic and Tactical Disconnections for C−C Bond Construction

Angewandte Chemie International Edition, 2021-07, Vol.60 (29), p.15767-15790

International ed. in English, 2021

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Controlling Pd(iv) reductive elimination pathways enables Pd(ii)-catalysed enantioselective C(sp3)−H fluorination

Nature chemistry, 2018-07, Vol.10 (7), p.755-762

2018

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A Review on the Latest Progress of Chan‐Lam Coupling Reaction

Advanced synthesis & catalysis, 2020-08, Vol.362 (16), p.3311-3331

2020

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Remote meta-CH Olefination of Phenylacetic Acids Directed by a Versatile U-Shaped Template

Angewandte Chemie International Edition, 2015-01, Vol.54 (3), p.888-891

2015

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Enantioselective C(sp 3 )‒H bond activation by chiral transition metal catalysts

Science (American Association for the Advancement of Science), 2018-02, Vol.359 (6377)

2018

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From Pd(OAc)2 to Chiral Catalysts: The Discovery and Development of Bifunctional Mono-N-Protected Amino Acid Ligands for Diverse C–H Functionalization Reactions

Accounts of chemical research, 2020-04, Vol.53 (4), p.833-851

2020

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Remote site-selective C–H activation directed by a catalytic bifunctional template

Nature (London), 2017-03, Vol.543 (7646), p.538-542

2017

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A Simple and Versatile Amide Directing Group for C−H Functionalizations

Angewandte Chemie International Edition, 2016-08, Vol.55 (36), p.10578-10599

International ed. in English, 2016

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meta‐C−H Arylation and Alkylation of Benzylsulfonamide Enabled by a Palladium(II)/Isoquinoline Catalyst

Angewandte Chemie International Edition, 2017-07, Vol.56 (28), p.8183-8186

International ed. in English, 2017

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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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Synthesis of Cyclic Anhydrides via Ligand‐Enabled C–H Carbonylation of Simple Aliphatic Acids

Angewandte Chemie International Edition, 2021-07, Vol.60 (30), p.16382-16387

International ed. in English, 2021

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β‐ and γ‐C(sp3)−H Heteroarylation of Free Carboxylic Acids: A Modular Synthetic Platform for Diverse Quaternary Carbon Centers

Angewandte Chemie International Edition, 2023-02, Vol.62 (9), p.e202214459-n/a

International ed. in English, 2023

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Lactonization as a general route to β-C(sp3)–H functionalization

Nature (London), 2020-01, Vol.577 (7792), p.656-659

2020

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Room-temperature enantioselective C–H iodination via kinetic resolution

Science (American Association for the Advancement of Science), 2014-10, Vol.346 (6208), p.451-455

2014

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Pd(II)-Catalyzed Enantioselective γ‑C(sp3)–H Functionalizations of Free Cyclopropylmethylamines

Journal of the American Chemical Society, 2020-07, Vol.142 (28), p.12015-12019

2020

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Practical Alkoxythiocarbonyl Auxiliaries for Iridium(I)‐Catalyzed C−H Alkylation of Azacycles

Angewandte Chemie International Edition, 2017-08, Vol.56 (35), p.10530-10534

International ed. in English, 2017

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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 Edition, 2017-08, Vol.56 (36), p.10924-10927

International ed. in English, 2017

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Copper‐Catalyzed Bromination of C(sp3)−H Bonds Distal to Functional Groups

Angewandte Chemie International Edition, 2017-01, Vol.56 (1), p.306-309

International ed. in English, 2017

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Palladium-Catalyzed [3 + 2] Cycloaddition via Twofold 1,3-C(sp3)–H Activation

Journal of the American Chemical Society, 2020-09, Vol.142 (39), p.16552-16556

2020

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Conformation-induced remote meta-C–H activation of amines

Nature (London), 2014-03, Vol.507 (7491), p.215-220

2014

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Utilizing Carbonyl Coordination of Native Amides for Palladium‐Catalyzed C(sp3)−H Olefination

Angewandte Chemie International Edition, 2019-08, Vol.58 (33), p.11424-11428

International ed. in English, 2019

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Recent Advances and Future Perspectives in Cotton Research

Annual review of plant biology, 2021-06, Vol.72 (1), p.437-462

2021

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Ligand‐Promoted meta‐C−H Functionalization of Benzylamines

Angewandte Chemie International Edition, 2017-04, Vol.56 (18), p.5125-5129

International ed. in English, 2017

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Functionalization of C(sp³)-H bonds using a transient directing group

Science (American Association for the Advancement of Science), 2016-01, Vol.351 (6270), p.252-256

2016

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Activation of remote meta-C–H bonds assisted by an end-on template

Nature (London), 2012-06, Vol.486 (7404), p.518-522

2012

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Advancing the Logic of Chemical Synthesis: C−H Activation as Strategic and Tactical Disconnections for C−C Bond Construction

Controlling Pd(iv) reductive elimination pathways enables Pd(ii)-catalysed enantioselective C(sp3)−H fluorination

A Review on the Latest Progress of Chan‐Lam Coupling Reaction

Remote meta-CH Olefination of Phenylacetic Acids Directed by a Versatile U-Shaped Template

Enantioselective C(sp 3 )‒H bond activation by chiral transition metal catalysts

From Pd(OAc)2 to Chiral Catalysts: The Discovery and Development of Bifunctional Mono-N-Protected Amino Acid Ligands for Diverse C–H Functionalization Reactions

Remote site-selective C–H activation directed by a catalytic bifunctional template

A Simple and Versatile Amide Directing Group for C−H Functionalizations

meta‐C−H Arylation and Alkylation of Benzylsulfonamide Enabled by a Palladium(II)/Isoquinoline Catalyst

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

Synthesis of Cyclic Anhydrides via Ligand‐Enabled C–H Carbonylation of Simple Aliphatic Acids

β‐ and γ‐C(sp3)−H Heteroarylation of Free Carboxylic Acids: A Modular Synthetic Platform for Diverse Quaternary Carbon Centers

Lactonization as a general route to β-C(sp3)–H functionalization

Room-temperature enantioselective C–H iodination via kinetic resolution

Pd(II)-Catalyzed Enantioselective γ‑C(sp3)–H Functionalizations of Free Cyclopropylmethylamines

Practical Alkoxythiocarbonyl Auxiliaries for Iridium(I)‐Catalyzed C−H Alkylation of Azacycles

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

Copper‐Catalyzed Bromination of C(sp3)−H Bonds Distal to Functional Groups

Palladium-Catalyzed [3 + 2] Cycloaddition via Twofold 1,3-C(sp3)–H Activation

Conformation-induced remote meta-C–H activation of amines

Utilizing Carbonyl Coordination of Native Amides for Palladium‐Catalyzed C(sp3)−H Olefination

Recent Advances and Future Perspectives in Cotton Research

Ligand‐Promoted meta‐C−H Functionalization of Benzylamines

Functionalization of C(sp³)-H bonds using a transient directing group

Activation of remote meta-C–H bonds assisted by an end-on template

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