Reactivity of (bi-Oxazoline)organonickel Complexes and Revision of a Catalytic Mechanism

Redox Activity of Pyridine-Oxazoline Ligands in the Stabilization of Low-Valent Organonickel Radical Complexes

(2021) Clifton L. Wagner et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

Monovalent Nickel-Mediated Radical Formation: A Concerted Halogen-Atom Dissociation Pathway Determined by Electroanalytical Studies

(2021) Qiao Lin et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

Experimental Electrochemical Potentials of Nickel Complexes

(2021) Tianning Diao et al.   SYNLETT

Mechanisms of Nickel-Catalyzed Coupling Reactions and Applications in Alkene Functionalization

(2020) Justin Diccianni et al.   ACCOUNTS OF CHEMICAL RESEARCH

Enantioselective Three-Component Fluoroalkylarylation of Unactivated Olefins through Nickel-Catalyzed Cross-Electrophile Coupling

(2020) Hai-Yong Tu et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

General Method for Enantioselective Three-Component Carboarylation of Alkenes Enabled by Visible-Light Dual Photoredox/Nickel Catalysis

(2020) Lei Guo et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

Mechanistic Characterization of (Xantphos)Ni(I)-Mediated Alkyl Bromide Activation: Oxidative Addition, Electron Transfer, or Halogen-Atom Abstraction

(2019) Justin B. Diccianni et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

Ni(I)–X Complexes Bearing a Bulky α-Diimine Ligand: Synthesis, Structure, and Superior Catalytic Performance in the Hydrogen Isotope Exchange in Pharmaceuticals

(2019) Cayetana Zarate et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

Synthesis and Reactivity of Paramagnetic Nickel Polypyridyl Complexes Relevant to C(sp2 )-C(sp3 )Coupling Reactions

(2019) Megan Mohadjer Beromi et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Nickel-Catalyzed Asymmetric Reductive Diarylation of Vinylarenes

(2019) David Anthony et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Site‐Selective, Remote sp3 C–H Carboxylation Enabled by the Merger of Photoredox and Nickel Catalysis

(2019) Ruben Martin et al.   CHEMISTRY-A EUROPEAN JOURNAL

Mechanistic Investigation of Enantioconvergent Kumada Reactions of Racemic α-Bromoketones Catalyzed by a Nickel/Bis(oxazoline) Complex

(2019) Haolin Yin et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

Mechanism of Ni-Catalyzed Reductive 1,2-Dicarbofunctionalization of Alkenes

(2019) Qiao Lin et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

Synthesis of Enantioenriched Allylic Silanes via Nickel-Catalyzed Reductive Cross-Coupling

(2017) Julie L. Hofstra et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

Activation of Small Molecules at Nickel(I) Moieties

(2017) Philipp Zimmermann et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

Nickel-Catalyzed Asymmetric Reductive Cross-Coupling To Access 1,1-Diarylalkanes

(2017) Kelsey E. Poremba et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

Nickel-Catalyzed Enantioselective Reductive Cross-Coupling of Styrenyl Aziridines

(2017) Brian P. Woods et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

Nickel Catalyzed Regio-, Diastereo-, and Enantioselective Cross-Coupling of 3,4-Epoxyalcohol with Aryl Iodides

(2017) Amit Banerjee et al.   ORGANIC LETTERS

Transition-Metal Catalysis of Nucleophilic Substitution Reactions: A Radical Alternative to SN1 and SN2 Processes

(2017) Gregory C. Fu   ACS Central Science

Ni(I)-Catalyzed Reductive Cyclization of 1,6-Dienes: Mechanism-Controlled trans Selectivity

(2017) Yulong Kuang et al.   Chem

C–H functionalization of amines with aryl halides by nickel-photoredox catalysis

(2016) Derek T. Ahneman et al.   Chemical Science

α-Arylation/Heteroarylation of Chiral α-Aminomethyltrifluoroborates by Synergistic Iridium Photoredox/Nickel Cross-Coupling Catalysis

(2015) Mirna El Khatib et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Single-Electron Transmetalation: Synthesis of 1,1-Diaryl-2,2,2-trifluoroethanes by Photoredox/Nickel Dual Catalytic Cross-Coupling

(2015) DaWeon Ryu et al.   CHEMISTRY-A EUROPEAN JOURNAL

Nickel-Catalyzed Cross-Coupling of Photoredox-Generated Radicals: Uncovering a General Manifold for Stereoconvergence in Nickel-Catalyzed Cross-Couplings

(2015) Osvaldo Gutierrez et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

Organometallic Nickel(III) Complexes Relevant to Cross-Coupling and Carbon–Heteroatom Bond Formation Reactions

(2014) Bo Zheng et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

Nickel-Catalyzed Negishi Arylations of Propargylic Bromides: A Mechanistic Investigation

(2014) Nathan D. Schley et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

Recent advances in homogeneous nickel catalysis

(2014) Sarah Z. Tasker et al.   NATURE

Single-electron transmetalation in organoboron cross-coupling by photoredox/nickel dual catalysis

(2014) J. C. Tellis et al.   SCIENCE

Synthesis, structure and electrochemical properties of the organonickel complex [NiBr(Mes)(phen)] (Mes = 2,4,6-trimethylphenyl, phen = 1,10-phenanthroline)

(2013) Dmitry G. Yakhvarov et al.   JOURNAL OF ORGANOMETALLIC CHEMISTRY

Nickel/Bis(oxazoline)-Catalyzed Asymmetric Negishi Arylations of Racemic Secondary Benzylic Electrophiles to Generate Enantioenriched 1,1-Diarylalkanes

(2013) Hien-Quang Do et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

Synthesis and Reactivity of Nickel Hydride Complexes of an α-Diimine Ligand

(2012) Qingsong Dong et al.   INORGANIC CHEMISTRY

Nickel-catalyzed cross coupling of non-activated alkyl halides: a mechanistic perspective

(2011) Xile Hu   Chemical Science

Nickel/Bis(oxazoline)-Catalyzed Asymmetric Kumada Reactions of Alkyl Electrophiles: Cross-Couplings of Racemic α-Bromoketones

(2010) Sha Lou et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

Geometric and Electronic Structures of the NiIand Methyl−NiIIIIntermediates of Methyl-Coenzyme M Reductase†

(2009) Ritimukta Sarangi et al.   BIOCHEMISTRY

Neutral Bis(α-iminopyridine)metal Complexes of the First-Row Transition Ions (Cr, Mn, Fe, Co, Ni, Zn) and Their Monocationic Analogues:  Mixed Valency Involving a Redox Noninnocent Ligand System

(2008) Connie C. Lu et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY