![Ni(II)-Catalyzed Intramolecular C–H/C–H Oxidative Coupling: An Efficient Route to Functionalized Cycloindolones and Indenoindolones | ACS Catalysis Ni(II)-Catalyzed Intramolecular C–H/C–H Oxidative Coupling: An Efficient Route to Functionalized Cycloindolones and Indenoindolones | ACS Catalysis](https://pubs.acs.org/cms/10.1021/acscatal.1c03314/asset/images/large/cs1c03314_0004.jpeg)
Ni(II)-Catalyzed Intramolecular C–H/C–H Oxidative Coupling: An Efficient Route to Functionalized Cycloindolones and Indenoindolones | ACS Catalysis
![Stereospecific/stereoselective nickel catalyzed reductive cross-coupling: An efficient tool for the synthesis of biological active targeted molecules - ScienceDirect Stereospecific/stereoselective nickel catalyzed reductive cross-coupling: An efficient tool for the synthesis of biological active targeted molecules - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S1319610322001715-gr38.jpg)
Stereospecific/stereoselective nickel catalyzed reductive cross-coupling: An efficient tool for the synthesis of biological active targeted molecules - ScienceDirect
![Nickel-Catalyzed Biaryl Coupling of Heteroarenes and Aryl Halides/Triflates | Itami Organic Chemistry Laboratory, Nagoya University Nickel-Catalyzed Biaryl Coupling of Heteroarenes and Aryl Halides/Triflates | Itami Organic Chemistry Laboratory, Nagoya University](http://synth.chem.nagoya-u.ac.jp/wordpress/wp-content/uploads/2009/06/jeromeorglett2009.jpg)
Nickel-Catalyzed Biaryl Coupling of Heteroarenes and Aryl Halides/Triflates | Itami Organic Chemistry Laboratory, Nagoya University
![Naked d-orbital in a centrochiral Ni(II) complex as a catalyst for asymmetric [3+2] cycloaddition | Nature Communications Naked d-orbital in a centrochiral Ni(II) complex as a catalyst for asymmetric [3+2] cycloaddition | Nature Communications](https://media.springernature.com/m685/springer-static/image/art%3A10.1038%2Fncomms14875/MediaObjects/41467_2017_Article_BFncomms14875_Fig5_HTML.jpg)
Naked d-orbital in a centrochiral Ni(II) complex as a catalyst for asymmetric [3+2] cycloaddition | Nature Communications
![Ni(OAc)2: a highly efficient catalyst for the synthesis of enaminone and enamino ester derivatives under solvent‐free conditions - Liu - 2010 - Applied Organometallic Chemistry - Wiley Online Library Ni(OAc)2: a highly efficient catalyst for the synthesis of enaminone and enamino ester derivatives under solvent‐free conditions - Liu - 2010 - Applied Organometallic Chemistry - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/082ae1f2-e783-4978-a5dd-e12d859cd373/msch001.gif)
Ni(OAc)2: a highly efficient catalyst for the synthesis of enaminone and enamino ester derivatives under solvent‐free conditions - Liu - 2010 - Applied Organometallic Chemistry - Wiley Online Library
![Synthesis, Crystal Structure, Fluorescence Property, and Theoretical Investigation of Counteranion-Introduced Ni(II) Complex with Pyridine-Appended Half-Salamo-Like Ligand | SpringerLink Synthesis, Crystal Structure, Fluorescence Property, and Theoretical Investigation of Counteranion-Introduced Ni(II) Complex with Pyridine-Appended Half-Salamo-Like Ligand | SpringerLink](https://media.springernature.com/lw685/springer-static/image/art%3A10.1134%2FS0036023623601198/MediaObjects/11502_2023_2970_Fig1_HTML.png)
Synthesis, Crystal Structure, Fluorescence Property, and Theoretical Investigation of Counteranion-Introduced Ni(II) Complex with Pyridine-Appended Half-Salamo-Like Ligand | SpringerLink
One to Find Them All: A General Route to Ni(I)–Phenolate Species | Journal of the American Chemical Society
![General Method for the Amination of Aryl Halides with Primary and Secondary Alkyl Amines via Nickel Photocatalysis General Method for the Amination of Aryl Halides with Primary and Secondary Alkyl Amines via Nickel Photocatalysis](https://www.organic-chemistry.org/abstracts/lit8/598o.gif)
General Method for the Amination of Aryl Halides with Primary and Secondary Alkyl Amines via Nickel Photocatalysis
![Ni‐Catalyzed Regioselective C‐5 Halogenation of 8‐Aminoquinoline and Co‐Catalyzed Chelation Assisted C−H Iodination of Aromatic Sulfonamides with Molecular Iodine - Fernandes - 2022 - Chemistry – An Asian Journal - Wiley Online Library Ni‐Catalyzed Regioselective C‐5 Halogenation of 8‐Aminoquinoline and Co‐Catalyzed Chelation Assisted C−H Iodination of Aromatic Sulfonamides with Molecular Iodine - Fernandes - 2022 - Chemistry – An Asian Journal - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/8edc1e26-d2b5-40a5-adc7-5863764cb759/asia202200874-toc-0001-m.jpg)
Ni‐Catalyzed Regioselective C‐5 Halogenation of 8‐Aminoquinoline and Co‐Catalyzed Chelation Assisted C−H Iodination of Aromatic Sulfonamides with Molecular Iodine - Fernandes - 2022 - Chemistry – An Asian Journal - Wiley Online Library
![Polymers | Free Full-Text | Mononuclear Nickel(II) Complexes with Schiff Base Ligands: Synthesis, Characterization, and Catalytic Activity in Norbornene Polymerization Polymers | Free Full-Text | Mononuclear Nickel(II) Complexes with Schiff Base Ligands: Synthesis, Characterization, and Catalytic Activity in Norbornene Polymerization](https://www.mdpi.com/polymers/polymers-09-00105/article_deploy/html/images/polymers-09-00105-sch003-550.jpg)
Polymers | Free Full-Text | Mononuclear Nickel(II) Complexes with Schiff Base Ligands: Synthesis, Characterization, and Catalytic Activity in Norbornene Polymerization
![Reactions of Schiff Base‐Substituted Diselenides and ‐tellurides with Ni(II), Pd(II) and Pt(II) Phosphine Complexes - Roca Jungfer - 2020 - European Journal of Inorganic Chemistry - Wiley Online Library Reactions of Schiff Base‐Substituted Diselenides and ‐tellurides with Ni(II), Pd(II) and Pt(II) Phosphine Complexes - Roca Jungfer - 2020 - European Journal of Inorganic Chemistry - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/156ed1f1-3886-41bd-b27c-f0569350fc0d/ejic202000750-toc-0001-m.png)
Reactions of Schiff Base‐Substituted Diselenides and ‐tellurides with Ni(II), Pd(II) and Pt(II) Phosphine Complexes - Roca Jungfer - 2020 - European Journal of Inorganic Chemistry - Wiley Online Library
![SYNTHESIS, SPECTROSCOPIC INVESTIGATION AND CATALYTIC STUDIES OF NICKEL(II) AROMATIC AZOMETHINE COMPLEXES | Semantic Scholar SYNTHESIS, SPECTROSCOPIC INVESTIGATION AND CATALYTIC STUDIES OF NICKEL(II) AROMATIC AZOMETHINE COMPLEXES | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/381decb84a74f5a2b51f96fecbbb725c07e2a801/3-Figure2-1.png)
SYNTHESIS, SPECTROSCOPIC INVESTIGATION AND CATALYTIC STUDIES OF NICKEL(II) AROMATIC AZOMETHINE COMPLEXES | Semantic Scholar
![IJMS | Free Full-Text | Mild and Efficient Heterogeneous Hydrogenation of Nitroarenes Facilitated by a Pyrolytically Activated Dinuclear Ni(II)-Ce(III) Diimine Complex IJMS | Free Full-Text | Mild and Efficient Heterogeneous Hydrogenation of Nitroarenes Facilitated by a Pyrolytically Activated Dinuclear Ni(II)-Ce(III) Diimine Complex](https://www.mdpi.com/ijms/ijms-23-08742/article_deploy/html/images/ijms-23-08742-sch002.png)