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C-H bond activation enables the rapid construction and late-stage diversification of functional molecules

Nature chemistry, 2013-05, Vol.5 (5), p.369

2013

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Organocatalytic umpolung: N-heterocyclic carbenes and beyond

Chemical Society reviews, 2012-01, Vol.41 (9), p.3511-3522

2012

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Measure of All Rings--N-Heterocyclic Carbenes

Angewandte Chemie (International ed.), 2010-09, Vol.49 (39), p.6940-6952

2010

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Asymmetric Cross-Coupling of Non-Activated Secondary Alkyl Halides

Angewandte Chemie (International ed.), 2008-10, Vol.47 (44), p.8347-8349

Glorius, Frank

2008

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Rapid Assessment of the Reaction‐Condition‐Based Sensitivity of Chemical Transformations

Angewandte Chemie International Edition, 2019-06, Vol.58 (25), p.8572-8576

International ed. in English, 2019

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Transition-Metal-Free, Visible-Light-Enabled Decarboxylative Borylation of Aryl N‑Hydroxyphthalimide Esters

Journal of the American Chemical Society, 2017-06, Vol.139 (22), p.7440-7443

2017

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Asymmetric hydrogenation of aromatic compounds

Organic & biomolecular chemistry, 2005, Vol.3 (23), p.4171

Glorius, Frank

2005

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Formal SN-Type Reactions in Rhodium(III)-Catalyzed CH Bond Activation

Advanced synthesis & catalysis, 2014-05, Vol.356 (7), p.1443-1460

2014

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C–H Activation: Toward Sustainability and Applications

ACS central science, 2021-02, Vol.7 (2), p.245-261

2021

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Privileged chiral N-heterocyclic carbene ligands for asymmetric transition-metal catalysis

Chemical Society reviews, 2017-08, Vol.46 (16), p.4845-4854

2017

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Indole Synthesis by Rhodium(III)-Catalyzed Hydrazine-Directed CH Activation: Redox-Neutral and Traceless by NN Bond Cleavage

Angewandte Chemie (International ed.), 2013-11, Vol.52 (47), p.12426-12429

2013

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A robustness screen for the rapid assessment of chemical reactions

Nature chemistry, 2013-07, Vol.5 (7), p.597

2013

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Reductive radical-polar crossover: traditional electrophiles in modern radical reactions

Chemical science (Cambridge), 2019-09, Vol.1 (36), p.8285-8291

2019

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Selective Arene Hydrogenation for Direct Access to Saturated Carbo‐ and Heterocycles

Angewandte Chemie (International ed.), 2019-07, Vol.58 (31), p.10460-10476

International ed. in English, 2019

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A Comparative Investigation: Group 9 CpM(III)-Catalyzed Formal [4 + 2] Cycloaddition as an Atom-Economic Approach to Quinazolines

Organic letters, 2016-05, Vol.18 (9), p.2090-2093

2016

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N‑Heterocyclic Carbenes in Asymmetric Hydrogenation

ACS catalysis, 2016-09, Vol.6 (9), p.5978-5988

2016

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Combining Gold and Photoredox Catalysis: Visible Light-Mediated Oxy- and Aminoarylation of Alkenes

Journal of the American Chemical Society, 2013-04, Vol.135 (15), p.5505-5508

2013

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Molecular Machine Learning: The Future of Synthetic Chemistry?

Angewandte Chemie International Edition, 2020-10, Vol.59 (43), p.18860-18865

International ed. in English, 2020

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Visible‐Light‐Photosensitized Aryl and Alkyl Decarboxylative Functionalization Reactions

Angewandte Chemie International Edition, 2019-07, Vol.58 (31), p.10514-10520

International ed. in English, 2019

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Beyond Directing Groups: Transition-Metal-Catalyzed CH Activation of Simple Arenes

Angewandte Chemie (International ed.), 2012-10, Vol.51 (41), p.10236-10254

2012

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Highly Enantioselective [5 + 2] Annulations through Cooperative N‑Heterocyclic Carbene (NHC) Organocatalysis and Palladium Catalysis

Journal of the American Chemical Society, 2018-03, Vol.140 (10), p.3551-3554

2018

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Increasing Catalyst Efficiency in C−H Activation Catalysis

Angewandte Chemie International Edition, 2018-02, Vol.57 (9), p.2296-2306

International ed. in English, 2018

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Approach to Comparing the Functional Group Tolerance of Reactions

Journal of organic chemistry, 2017-09, Vol.82 (17), p.9154-9159

2017

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Rh(III)-Catalyzed Directed C−H Olefination Using an Oxidizing Directing Group: Mild, Efficient, and Versatile

Journal of the American Chemical Society, 2011-03, Vol.133 (8), p.2350-2353

2011

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Rh Catalyzed Olefination and Vinylation of Unactivated Acetanilides

Journal of the American Chemical Society, 2010-07, Vol.132 (29), p.9982-9983

2010

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C-H bond activation enables the rapid construction and late-stage diversification of functional molecules

Organocatalytic umpolung: N-heterocyclic carbenes and beyond

Measure of All Rings--N-Heterocyclic Carbenes

Asymmetric Cross-Coupling of Non-Activated Secondary Alkyl Halides

Rapid Assessment of the Reaction‐Condition‐Based Sensitivity of Chemical Transformations

Transition-Metal-Free, Visible-Light-Enabled Decarboxylative Borylation of Aryl N‑Hydroxyphthalimide Esters

Asymmetric hydrogenation of aromatic compounds

Formal SN-Type Reactions in Rhodium(III)-Catalyzed CH Bond Activation

C–H Activation: Toward Sustainability and Applications

Privileged chiral N-heterocyclic carbene ligands for asymmetric transition-metal catalysis

Indole Synthesis by Rhodium(III)-Catalyzed Hydrazine-Directed CH Activation: Redox-Neutral and Traceless by NN Bond Cleavage

A robustness screen for the rapid assessment of chemical reactions

Reductive radical-polar crossover: traditional electrophiles in modern radical reactions

Selective Arene Hydrogenation for Direct Access to Saturated Carbo‐ and Heterocycles

A Comparative Investigation: Group 9 CpM(III)-Catalyzed Formal [4 + 2] Cycloaddition as an Atom-Economic Approach to Quinazolines

N‑Heterocyclic Carbenes in Asymmetric Hydrogenation

Combining Gold and Photoredox Catalysis: Visible Light-Mediated Oxy- and Aminoarylation of Alkenes

Molecular Machine Learning: The Future of Synthetic Chemistry?

Visible‐Light‐Photosensitized Aryl and Alkyl Decarboxylative Functionalization Reactions

Beyond Directing Groups: Transition-Metal-Catalyzed CH Activation of Simple Arenes

Highly Enantioselective [5 + 2] Annulations through Cooperative N‑Heterocyclic Carbene (NHC) Organocatalysis and Palladium Catalysis

Increasing Catalyst Efficiency in C−H Activation Catalysis

Approach to Comparing the Functional Group Tolerance of Reactions

Rh(III)-Catalyzed Directed C−H Olefination Using an Oxidizing Directing Group: Mild, Efficient, and Versatile

Rh Catalyzed Olefination and Vinylation of Unactivated Acetanilides

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