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General Olefin Synthesis by the Palladium-Catalyzed Heck Reaction of Amides: Sterically Controlled Chemoselective NC Activation

Angewandte Chemie (International ed.), 2015-11, Vol.54 (48), p.14518-14522

International ed. in English, 2015

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Sterically Controlled Pd-Catalyzed Chemoselective Ketone Synthesis via N–C Cleavage in Twisted Amides

Organic letters, 2015-09, Vol.17 (17), p.4364-4367

2015

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N‐Acyl‐Glutarimides: Privileged Scaffolds in Amide N–C Bond Cross‐Coupling

European journal of organic chemistry, 2018-06, Vol.2018 (20-21), p.2352-2365

2018

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Synthesis of Biaryls through Nickel-Catalyzed Suzuki-Miyaura Coupling of Amides by Carbon-Nitrogen Bond Cleavage

Angewandte Chemie (International ed.), 2016-06, Vol.55 (24), p.6959-6963

International ed. in English, 2016

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Palladium-catalyzed Suzuki-Miyaura coupling of amides by carbon-nitrogen cleavage: general strategy for amide N-C bond activation

Organic & biomolecular chemistry, 2016-01, Vol.14 (24), p.5690-5707

2016

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N‑Heterocyclic Carbene Complexes in C–H Activation Reactions

Chemical reviews, 2020-02, Vol.120 (4), p.1981-2048

2020

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Cross-Coupling of Amides by N–C Bond Activation

Synlett, 2016-11, Vol.27 (18), p.2530-2540

2016

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Site-Selective C–H/C–N Activation by Cooperative Catalysis: Primary Amides as Arylating Reagents in Directed C–H Arylation

ACS catalysis, 2017-10, Vol.7 (10), p.7251-7256

2017

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A General Method for Two-Step Transamidation of Secondary Amides Using Commercially Available, Air- and Moisture-Stable Palladium/NHC (N‑Heterocyclic Carbene) Complexes

Organic letters, 2017-04, Vol.19 (8), p.2158-2161

2017

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General Method for the Suzuki–Miyaura Cross-Coupling of Amides Using Commercially Available, Air- and Moisture-Stable Palladium/NHC (NHC = N‑Heterocyclic Carbene) Complexes

ACS catalysis, 2017-03, Vol.7 (3), p.1960-1965

2017

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Reversible Twisting of Primary Amides via Ground State N–C(O) Destabilization: Highly Twisted Rotationally Inverted Acyclic Amides

Journal of the American Chemical Society, 2018-01, Vol.140 (2), p.727-734

2018

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Suzuki–Miyaura Cross-Coupling of N‑Acylpyrroles and Pyrazoles: Planar, Electronically Activated Amides in Catalytic N–C Cleavage

Organic letters, 2017-07, Vol.19 (13), p.3596-3599

2017

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N‑Acylsaccharins as Amide-Based Arylating Reagents via Chemoselective N–C Cleavage: Pd-Catalyzed Decarbonylative Heck Reaction

Journal of organic chemistry, 2016-12, Vol.81 (23), p.12023-12030

2016

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Ground-State Distortion in N‑Acyl-tert-butyl-carbamates (Boc) and N‑Acyl-tosylamides (Ts): Twisted Amides of Relevance to Amide N–C Cross-Coupling

Journal of organic chemistry, 2016-09, Vol.81 (17), p.8091-8094

2016

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Pd-PEPPSI: Pd-NHC Precatalyst for Suzuki–Miyaura Cross-Coupling Reactions of Amides

Journal of organic chemistry, 2017-07, Vol.82 (13), p.6638-6646

2017

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Achieving Site-Selectivity for C-H Activation Processes Based on Distance and Geometry: A Carpenter's Approach

Journal of the American Chemical Society, 2020-06, Vol.142 (24), p.10571-10591

2020

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Structures of Highly Twisted Amides Relevant to Amide N−C Cross-Coupling: Evidence for Ground-State Amide Destabilization

Chemistry : a European journal, 2016-10, Vol.22 (41), p.14494-14498

2016

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N‑Acylsaccharins: Stable Electrophilic Amide-Based Acyl Transfer Reagents in Pd-Catalyzed Suzuki–Miyaura Coupling via N–C Cleavage

Organic letters, 2016-09, Vol.18 (17), p.4194-4197

2016

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General Method for the Suzuki–Miyaura Cross-Coupling of Primary Amide-Derived Electrophiles Enabled by [Pd(NHC)(cin)Cl] at Room Temperature

Organic letters, 2017-12, Vol.19 (24), p.6510-6513

2017

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Rhodium-Catalyzed C–H Bond Functionalization with Amides by Double C–H/C–N Bond Activation

Organic letters, 2016-02, Vol.18 (4), p.796-799

2016

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[IPr # -PEPPSI]: A Well-Defined, Highly Hindered and Broadly Applicable Pd(II)-NHC (NHC = N-Heterocyclic Carbene) Precatalyst for Cross-Coupling Reactions

Molecules (Basel, Switzerland), 2023-08, Vol.28 (15), p.5833

2023

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Acyclic Twisted Amides

Chemical reviews, 2021-10, Vol.121 (20), p.12746-12783

2021

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Palladium-Catalyzed Suzuki–Miyaura Cross-Coupling of Amides via Site-Selective N–C Bond Cleavage by Cooperative Catalysis

ACS catalysis, 2016-11, Vol.6 (11), p.7335-7339

2016

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A novel full-human CD22-CAR T cell therapy with potent activity against CD22low B-ALL

Blood cancer journal (New York), 2021-04, Vol.11 (4), p.71-71, Article 71

2021

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Resonance Destabilization in N‑Acylanilines (Anilides): Electronically-Activated Planar Amides of Relevance in N–C(O) Cross-Coupling

Journal of organic chemistry, 2017-06, Vol.82 (12), p.6373-6378

2017

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General Olefin Synthesis by the Palladium-Catalyzed Heck Reaction of Amides: Sterically Controlled Chemoselective NC Activation

Sterically Controlled Pd-Catalyzed Chemoselective Ketone Synthesis via N–C Cleavage in Twisted Amides

N‐Acyl‐Glutarimides: Privileged Scaffolds in Amide N–C Bond Cross‐Coupling

Synthesis of Biaryls through Nickel-Catalyzed Suzuki-Miyaura Coupling of Amides by Carbon-Nitrogen Bond Cleavage

Palladium-catalyzed Suzuki-Miyaura coupling of amides by carbon-nitrogen cleavage: general strategy for amide N-C bond activation

N‑Heterocyclic Carbene Complexes in C–H Activation Reactions

Cross-Coupling of Amides by N–C Bond Activation

Site-Selective C–H/C–N Activation by Cooperative Catalysis: Primary Amides as Arylating Reagents in Directed C–H Arylation

A General Method for Two-Step Transamidation of Secondary Amides Using Commercially Available, Air- and Moisture-Stable Palladium/NHC (N‑Heterocyclic Carbene) Complexes

General Method for the Suzuki–Miyaura Cross-Coupling of Amides Using Commercially Available, Air- and Moisture-Stable Palladium/NHC (NHC = N‑Heterocyclic Carbene) Complexes

Reversible Twisting of Primary Amides via Ground State N–C(O) Destabilization: Highly Twisted Rotationally Inverted Acyclic Amides

Suzuki–Miyaura Cross-Coupling of N‑Acylpyrroles and Pyrazoles: Planar, Electronically Activated Amides in Catalytic N–C Cleavage

N‑Acylsaccharins as Amide-Based Arylating Reagents via Chemoselective N–C Cleavage: Pd-Catalyzed Decarbonylative Heck Reaction

Ground-State Distortion in N‑Acyl-tert-butyl-carbamates (Boc) and N‑Acyl-tosylamides (Ts): Twisted Amides of Relevance to Amide N–C Cross-Coupling

Pd-PEPPSI: Pd-NHC Precatalyst for Suzuki–Miyaura Cross-Coupling Reactions of Amides

Achieving Site-Selectivity for C-H Activation Processes Based on Distance and Geometry: A Carpenter's Approach

Structures of Highly Twisted Amides Relevant to Amide N−C Cross-Coupling: Evidence for Ground-State Amide Destabilization

N‑Acylsaccharins: Stable Electrophilic Amide-Based Acyl Transfer Reagents in Pd-Catalyzed Suzuki–Miyaura Coupling via N–C Cleavage

General Method for the Suzuki–Miyaura Cross-Coupling of Primary Amide-Derived Electrophiles Enabled by [Pd(NHC)(cin)Cl] at Room Temperature

Rhodium-Catalyzed C–H Bond Functionalization with Amides by Double C–H/C–N Bond Activation

[IPr # -PEPPSI]: A Well-Defined, Highly Hindered and Broadly Applicable Pd(II)-NHC (NHC = N-Heterocyclic Carbene) Precatalyst for Cross-Coupling Reactions

Acyclic Twisted Amides

Palladium-Catalyzed Suzuki–Miyaura Cross-Coupling of Amides via Site-Selective N–C Bond Cleavage by Cooperative Catalysis

A novel full-human CD22-CAR T cell therapy with potent activity against CD22low B-ALL

Resonance Destabilization in N‑Acylanilines (Anilides): Electronically-Activated Planar Amides of Relevance in N–C(O) Cross-Coupling

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