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Stereodivergent, Kinetically Controlled Isomerization of Terminal Alkenes via Nickel Catalysis.
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- Angewandte Chemie, 2024, v. 136, n. 21, p. 1, doi. 10.1002/ange.202320081
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- Article
Stereodivergent, Kinetically Controlled Isomerization of Terminal Alkenes via Nickel Catalysis.
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- Angewandte Chemie International Edition, 2024, v. 63, n. 21, p. 1, doi. 10.1002/anie.202320081
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- Article
Nickel‐Electrocatalytic Decarboxylative Arylation to Access Quaternary Centers**.
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- Angewandte Chemie, 2024, v. 136, n. 8, p. 1, doi. 10.1002/ange.202314617
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- Article
Nickel‐Electrocatalytic Decarboxylative Arylation to Access Quaternary Centers**.
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- Angewandte Chemie International Edition, 2024, v. 63, n. 8, p. 1, doi. 10.1002/anie.202314617
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- Article
Electroreductive Synthesis of Nickel(0) Complexes.
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- Angewandte Chemie, 2024, v. 136, n. 2, p. 1, doi. 10.1002/ange.202311557
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- Article
Electroreductive Synthesis of Nickel(0) Complexes.
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- Angewandte Chemie International Edition, 2024, v. 63, n. 2, p. 1, doi. 10.1002/anie.202311557
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- Article
Catalytic σ‐Bond Annulation with Ambiphilic Organohalides Enabled by β‐X Elimination.
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- Angewandte Chemie, 2023, v. 135, n. 34, p. 1, doi. 10.1002/ange.202306581
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- Article
Catalytic σ‐Bond Annulation with Ambiphilic Organohalides Enabled by β‐X Elimination**.
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- Angewandte Chemie International Edition, 2023, v. 62, n. 34, p. 1, doi. 10.1002/anie.202306581
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- Article
Enantioselective Hydroalkenylation and Hydroalkynylation of Alkenes Enabled by a Transient Directing Group: Catalyst Generality through Rigidification**.
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- Angewandte Chemie, 2023, v. 135, n. 29, p. 1, doi. 10.1002/ange.202304013
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- Article
Enantioselective Hydroalkenylation and Hydroalkynylation of Alkenes Enabled by a Transient Directing Group: Catalyst Generality through Rigidification**.
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- Angewandte Chemie International Edition, 2023, v. 62, n. 29, p. 1, doi. 10.1002/anie.202304013
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- Article
Structurally Diverse Bench‐Stable Nickel(0) Pre‐Catalysts: A Practical Toolkit for In Situ Ligation Protocols**.
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- Angewandte Chemie, 2023, v. 135, n. 9, p. 1, doi. 10.1002/ange.202211794
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- Article
Structurally Diverse Bench‐Stable Nickel(0) Pre‐Catalysts: A Practical Toolkit for In Situ Ligation Protocols**.
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- Angewandte Chemie International Edition, 2023, v. 62, n. 9, p. 1, doi. 10.1002/anie.202211794
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- Article
A Sterically Tuned Directing Auxiliary Promotes Catalytic 1,2‐Carbofluorination of Alkenyl Carbonyl Compounds**.
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- Angewandte Chemie, 2023, v. 135, n. 4, p. 1, doi. 10.1002/ange.202214153
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- Article
A Sterically Tuned Directing Auxiliary Promotes Catalytic 1,2‐Carbofluorination of Alkenyl Carbonyl Compounds**.
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- Angewandte Chemie International Edition, 2023, v. 62, n. 4, p. 1, doi. 10.1002/anie.202214153
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- Article
Regio‐ and Stereoselective 1,2‐Oxyhalogenation of Non‐Conjugated Alkynes via Directed Nucleopalladation: Catalytic Access to Tetrasubstituted Alkenes**.
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- Angewandte Chemie, 2022, v. 134, n. 43, p. 1, doi. 10.1002/ange.202209099
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- Article
Regio‐ and Stereoselective 1,2‐Oxyhalogenation of Non‐Conjugated Alkynes via Directed Nucleopalladation: Catalytic Access to Tetrasubstituted Alkenes**.
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- Angewandte Chemie International Edition, 2022, v. 61, n. 43, p. 1, doi. 10.1002/anie.202209099
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- Article
Pd<sup>II</sup>‐Catalyzed C(alkenyl)−H Activation Facilitated by a Transient Directing Group**.
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- Angewandte Chemie, 2022, v. 134, n. 25, p. 1, doi. 10.1002/ange.202203624
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- Article
Pd<sup>II</sup>‐Catalyzed C(alkenyl)−H Activation Facilitated by a Transient Directing Group**.
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- Angewandte Chemie International Edition, 2022, v. 61, n. 25, p. 1, doi. 10.1002/anie.202203624
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- Article
Mapping Ambiphile Reactivity Trends in the Anti‐(Hetero)annulation of Non‐Conjugated Alkenes via Pd<sup>II</sup>/Pd<sup>IV</sup> Catalysis.
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- Angewandte Chemie, 2022, v. 134, n. 13, p. 1, doi. 10.1002/ange.202114346
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- Article
Mapping Ambiphile Reactivity Trends in the Anti‐(Hetero)annulation of Non‐Conjugated Alkenes via Pd<sup>II</sup>/Pd<sup>IV</sup> Catalysis.
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- Angewandte Chemie International Edition, 2022, v. 61, n. 13, p. 1, doi. 10.1002/anie.202114346
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- Article
Cyclic (Alkyl)(amino)carbene Ligands Enable Cu‐Catalyzed Markovnikov Protoboration and Protosilylation of Terminal Alkynes: A Versatile Portal to Functionalized Alkenes**.
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- Angewandte Chemie, 2021, v. 133, n. 36, p. 20024, doi. 10.1002/ange.202106107
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- Article
Cyclic (Alkyl)(amino)carbene Ligands Enable Cu‐Catalyzed Markovnikov Protoboration and Protosilylation of Terminal Alkynes: A Versatile Portal to Functionalized Alkenes**.
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- Angewandte Chemie International Edition, 2021, v. 60, n. 36, p. 19871, doi. 10.1002/anie.202106107
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- Article
Anti-selective [3+2] (Hetero)annulation of non-conjugated alkenes via directed nucleopalladation.
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- Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-020-20182-4
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- Article
Ligand‐Controlled Regiodivergence in Nickel‐Catalyzed Hydroarylation and Hydroalkenylation of Alkenyl Carboxylic Acids**.
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- Angewandte Chemie, 2020, v. 132, n. 51, p. 23506, doi. 10.1002/ange.202010840
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- Article
Ligand‐Controlled Regiodivergence in Nickel‐Catalyzed Hydroarylation and Hydroalkenylation of Alkenyl Carboxylic Acids**.
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- Angewandte Chemie International Edition, 2020, v. 59, n. 51, p. 23306, doi. 10.1002/anie.202010840
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- Article
A Transient‐Directing‐Group Strategy Enables Enantioselective Reductive Heck Hydroarylation of Alkenes.
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- Angewandte Chemie, 2020, v. 132, n. 23, p. 8970, doi. 10.1002/ange.202001069
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- Article
A Transient‐Directing‐Group Strategy Enables Enantioselective Reductive Heck Hydroarylation of Alkenes.
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- Angewandte Chemie International Edition, 2020, v. 59, n. 23, p. 8885, doi. 10.1002/anie.202001069
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- Article
Ni(COD)(DQ): An Air‐Stable 18‐Electron Nickel(0)–Olefin Precatalyst.
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- Angewandte Chemie, 2020, v. 132, n. 19, p. 7479, doi. 10.1002/ange.202000124
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- Article
Ni(COD)(DQ): An Air‐Stable 18‐Electron Nickel(0)–Olefin Precatalyst.
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- Angewandte Chemie International Edition, 2020, v. 59, n. 19, p. 7409, doi. 10.1002/anie.202000124
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- Article
Integrating Allyl Electrophiles into Nickel‐Catalyzed Conjunctive Cross‐Coupling.
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- Angewandte Chemie, 2020, v. 132, n. 18, p. 7095, doi. 10.1002/ange.201915454
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- Article
Integrating Allyl Electrophiles into Nickel‐Catalyzed Conjunctive Cross‐Coupling.
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- Angewandte Chemie International Edition, 2020, v. 59, n. 18, p. 7029, doi. 10.1002/anie.201915454
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- Article
Transition‐Metal‐Catalyzed 1,2‐Carboboration of Alkenes: Strategies, Mechanisms, and Stereocontrol.
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- Israel Journal of Chemistry, 2020, v. 60, n. 3/4, p. 219, doi. 10.1002/ijch.201900087
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- Article
Nickel‐Catalyzed 1,2‐Diarylation of Alkenyl Carboxylates: A Gateway to 1,2,3‐Trifunctionalized Building Blocks.
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- Angewandte Chemie, 2020, v. 132, n. 3, p. 1217, doi. 10.1002/ange.201913062
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- Article
Nickel‐Catalyzed 1,2‐Diarylation of Alkenyl Carboxylates: A Gateway to 1,2,3‐Trifunctionalized Building Blocks.
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- Angewandte Chemie International Edition, 2020, v. 59, n. 3, p. 1201, doi. 10.1002/anie.201913062
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- Article
Palladium(0)‐Catalyzed Directed syn‐1,2‐Carboboration and ‐Silylation: Alkene Scope, Applications in Dearomatization, and Stereocontrol by a Chiral Auxiliary.
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- Angewandte Chemie, 2019, v. 131, n. 47, p. 17224, doi. 10.1002/ange.201910304
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- Article
Palladium(0)‐Catalyzed Directed syn‐1,2‐Carboboration and ‐Silylation: Alkene Scope, Applications in Dearomatization, and Stereocontrol by a Chiral Auxiliary.
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- Angewandte Chemie International Edition, 2019, v. 58, n. 47, p. 17068, doi. 10.1002/anie.201910304
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- Article
Nickel-catalyzed intermolecular oxidative Heck arylation driven by transfer hydrogenation.
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- Nature Communications, 2019, v. 10, n. 1, p. 1, doi. 10.1038/s41467-019-12949-1
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- Article
Catalytic, Enantioselective α‐Alkylation of Azlactones with Nonconjugated Alkenes by Directed Nucleopalladation.
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- Angewandte Chemie, 2019, v. 131, n. 12, p. 3963, doi. 10.1002/ange.201814272
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- Article
Catalytic, Enantioselective α‐Alkylation of Azlactones with Nonconjugated Alkenes by Directed Nucleopalladation.
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- Angewandte Chemie International Edition, 2019, v. 58, n. 12, p. 3923, doi. 10.1002/anie.201814272
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- Article
The mechanism of palladium(II)-mediated C-H cleavage with mono- N-protected amino acid (MPAA) ligands: origins of rate acceleration.
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- Pure & Applied Chemistry, 2016, v. 88, n. 1/2, p. 119, doi. 10.1515/pac-2015-0902
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The mechanism of palladium(II)-mediated C-H cleavage with mono-N-protected amino acid (MPAA) ligands: origins of rate acceleration.
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- Pure & Applied Chemistry, 2016, v. 88, n. 1/2, p. 119, doi. 10.1515/pac-2015-0902
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- Article
Ligand-enabled meta-C-H activation using a transient mediator.
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- Nature, 2015, v. 519, n. 7543, p. 334, doi. 10.1038/nature14214
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- Article
Asymmetric Electrophilic Fluorocyclization with Carbon Nucleophiles.
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- Angewandte Chemie, 2013, v. 125, n. 37, p. 9978, doi. 10.1002/ange.201304845
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- Article
Asymmetric Electrophilic Fluorocyclization with Carbon Nucleophiles.
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- Angewandte Chemie International Edition, 2013, v. 52, n. 37, p. 9796, doi. 10.1002/anie.201304845
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- Article
Trifluoromethylation of Allylsilanes under Copper Catalysis.
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- Chemistry - A European Journal, 2012, v. 18, n. 28, p. 8583, doi. 10.1002/chem.201201707
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- Article
Passive F.
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- Angewandte Chemie, 2011, v. 123, n. 7, p. 1514, doi. 10.1002/ange.201005142
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- Article
Bystanding F.
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- Angewandte Chemie International Edition, 2011, v. 50, n. 7, p. 1478, doi. 10.1002/anie.201005142
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- Article
Cover Picture: Cross-Coupling of C(sp.
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- Israel Journal of Chemistry, 2010, v. 50, n. 5/6, p. 537, doi. 10.1002/ijch.201090011
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- Article
Cross-Coupling of C(sp.
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- Israel Journal of Chemistry, 2010, v. 50, n. 5/6, p. 605, doi. 10.1002/ijch.201000038
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- Article
Constructing Multiply Substituted Arenes Using Sequential Palladium(II)-Catalyzed CH Olefination.
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- Angewandte Chemie, 2010, v. 122, n. 35, p. 6305, doi. 10.1002/ange.201002077
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- Article