UB Paderborn / Katalog / Suche / in CDI

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

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

2014

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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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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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Pd(II)-Catalyzed Enantioselective C(sp3)–H Borylation

Journal of the American Chemical Society, 2017-03, Vol.139 (9), p.3344-3347

2017

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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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Palladium(0)/PAr3-Catalyzed Intermolecular Amination of C(sp3)H Bonds: Synthesis of β-Amino Acids

Angewandte Chemie International Edition, 2015-05, Vol.54 (22), p.6545-6549

2015

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Ligand‐Enabled Double γ‐C(sp3)−H Functionalization of Aliphatic Acids: One‐Step Synthesis of γ‐Arylated γ‐Lactones

Angewandte Chemie International Edition, 2023-12, Vol.62 (49), p.e202312331-n/a

International ed. in English, 2023

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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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Distal γ‐C(sp3)−H Olefination of Ketone Derivatives and Free Carboxylic Acids

Angewandte Chemie International Edition, 2020-07, Vol.59 (31), p.12853-12859

International ed. in English, 2020

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Catalyst-controlled site-selective methylene C-H lactonization of dicarboxylic acids

Science (American Association for the Advancement of Science), 2022-06, Vol.376 (6600), p.1481-1487

2022

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Weak Coordination as a Powerful Means for Developing Broadly Useful C–H Functionalization Reactions

Accounts of chemical research, 2012-06, Vol.45 (6), p.788-802

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

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

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

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

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

Room-temperature enantioselective C–H iodination via kinetic resolution

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

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

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

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

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

Pd(II)-Catalyzed Enantioselective C(sp3)–H Borylation

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

Palladium(0)/PAr3-Catalyzed Intermolecular Amination of C(sp3)H Bonds: Synthesis of β-Amino Acids

Ligand‐Enabled Double γ‐C(sp3)−H Functionalization of Aliphatic Acids: One‐Step Synthesis of γ‐Arylated γ‐Lactones

Ligand‐Promoted meta‐C−H Functionalization of Benzylamines

Distal γ‐C(sp3)−H Olefination of Ketone Derivatives and Free Carboxylic Acids

Catalyst-controlled site-selective methylene C-H lactonization of dicarboxylic acids

Weak Coordination as a Powerful Means for Developing Broadly Useful C–H Functionalization Reactions

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