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színhely íz Részben ni ii catalyzed fenntart szótag Elkerülhetetlen

Radical Mechanism of IrIII/NiII-Metallaphotoredox-Catalyzed C(sp3)–H  Functionalization Triggered by Proton-Coupled Electron Transfer:  Theoretical Insight | CCS Chem
Radical Mechanism of IrIII/NiII-Metallaphotoredox-Catalyzed C(sp3)–H Functionalization Triggered by Proton-Coupled Electron Transfer: Theoretical Insight | CCS Chem

Synthesis and catalytic activity of nickel(II) complexes containing NCN  pincer ligands - ScienceDirect
Synthesis and catalytic activity of nickel(II) complexes containing NCN pincer ligands - ScienceDirect

Ogoshi Research Group. Publication
Ogoshi Research Group. Publication

Ni-catalyzed regio- and stereo-defined intermolecular cross-electrophile  dialkylation of alkynes without directing group | Nature Communications
Ni-catalyzed regio- and stereo-defined intermolecular cross-electrophile dialkylation of alkynes without directing group | Nature Communications

Merging photoredox with nickel catalysis: Coupling of α-carboxyl  sp3-carbons with aryl halides | Science
Merging photoredox with nickel catalysis: Coupling of α-carboxyl sp3-carbons with aryl halides | Science

Overcoming limitations in dual photoredox/nickel-catalysed C–N  cross-couplings due to catalyst deactivation | Nature Catalysis
Overcoming limitations in dual photoredox/nickel-catalysed C–N cross-couplings due to catalyst deactivation | Nature Catalysis

Mechanisms of Nickel-Catalyzed Coupling Reactions and Applications in  Alkene Functionalization | Accounts of Chemical Research
Mechanisms of Nickel-Catalyzed Coupling Reactions and Applications in Alkene Functionalization | Accounts of Chemical Research

A highly active Ni(II)-triadamantylphosphine catalyst for  ultrahigh-molecular-weight polyethylene synthesis | Nature Communications
A highly active Ni(II)-triadamantylphosphine catalyst for ultrahigh-molecular-weight polyethylene synthesis | Nature Communications

Reaction condition controlled nickel(ii)-catalyzed C–C cross-coupling of  alcohols - Organic & Biomolecular Chemistry (RSC Publishing)
Reaction condition controlled nickel(ii)-catalyzed C–C cross-coupling of alcohols - Organic & Biomolecular Chemistry (RSC Publishing)

Ni(II)-Catalyzed Intramolecular C–H/C–H Oxidative Coupling: An Efficient  Route to Functionalized Cycloindolones and Indenoindolones,ACS Catalysis -  X-MOL
Ni(II)-Catalyzed Intramolecular C–H/C–H Oxidative Coupling: An Efficient Route to Functionalized Cycloindolones and Indenoindolones,ACS Catalysis - X-MOL

Ligand-Enabled Ni(II)-Catalyzed Hydroxylarylation of Unactivated Alkenes  With Molecular Oxygen | Catalysis | ChemRxiv | Cambridge Open Engage
Ligand-Enabled Ni(II)-Catalyzed Hydroxylarylation of Unactivated Alkenes With Molecular Oxygen | Catalysis | ChemRxiv | Cambridge Open Engage

Nickel: The “Spirited Horse” of Transition Metal Catalysis | ACS Catalysis
Nickel: The “Spirited Horse” of Transition Metal Catalysis | ACS Catalysis

Understanding Formation and Roles of Ni(II) Aryl Amido and Ni(III) Aryl  Amido Intermediates in Ni-Catalyzed Electrochemical Aryl Amination  Reactions | Catalysis | ChemRxiv | Cambridge Open Engage
Understanding Formation and Roles of Ni(II) Aryl Amido and Ni(III) Aryl Amido Intermediates in Ni-Catalyzed Electrochemical Aryl Amination Reactions | Catalysis | ChemRxiv | Cambridge Open Engage

Mechanisms of Nickel-Catalyzed Cross-Coupling Reactions: Trends in Chemistry
Mechanisms of Nickel-Catalyzed Cross-Coupling Reactions: Trends in Chemistry

Inorganics | Free Full-Text | Room Temperature Ni(II) Catalyzed  Hydrophosphination and Cyclotrimerization of Alkynes
Inorganics | Free Full-Text | Room Temperature Ni(II) Catalyzed Hydrophosphination and Cyclotrimerization of Alkynes

Ni(II)-(σ-Aryl) Complex: A Facile, Efficient Catalyst for Nickel-Catalyzed  Carbon−Nitrogen Coupling Reactions
Ni(II)-(σ-Aryl) Complex: A Facile, Efficient Catalyst for Nickel-Catalyzed Carbon−Nitrogen Coupling Reactions

Nickel-Catalyzed Alkene Functionalization Reactions — Diao Research Group
Nickel-Catalyzed Alkene Functionalization Reactions — Diao Research Group

A surprising mechanism lacking the Ni(0) state during the Ni(II)-catalyzed  P–C cross-coupling reaction performed in the absence of a reducing agent –  An experimental and a theoretical study
A surprising mechanism lacking the Ni(0) state during the Ni(II)-catalyzed P–C cross-coupling reaction performed in the absence of a reducing agent – An experimental and a theoretical study

4. In the lab, you attempted a Ni(II) catalyzed | Chegg.com
4. In the lab, you attempted a Ni(II) catalyzed | Chegg.com

Nickel catalysis: Insights for catalyst selection – InCatT – Innovative  Catalyst Technologies
Nickel catalysis: Insights for catalyst selection – InCatT – Innovative Catalyst Technologies

From Bis(silylene) and Bis(germylene) Pincer-Type Nickel(II) Complexes to  Isolable Intermediates of the Nickel-Catalyzed Sonogashira Cross-Coupling  Reaction | The Hartwig Group
From Bis(silylene) and Bis(germylene) Pincer-Type Nickel(II) Complexes to Isolable Intermediates of the Nickel-Catalyzed Sonogashira Cross-Coupling Reaction | The Hartwig Group

Reduced Graphene Oxide-Supported Nickel(II)-Bis(1,10-Phenanthroline)  Complex as a Highly Active Electrocatalyst for Ethanol Oxidation Reaction |  SpringerLink
Reduced Graphene Oxide-Supported Nickel(II)-Bis(1,10-Phenanthroline) Complex as a Highly Active Electrocatalyst for Ethanol Oxidation Reaction | SpringerLink

PDF] Mechanisms of Nickel-Catalyzed Cross-Coupling Reactions | Semantic  Scholar
PDF] Mechanisms of Nickel-Catalyzed Cross-Coupling Reactions | Semantic Scholar

Organonickel chemistry - Wikipedia
Organonickel chemistry - Wikipedia