![Transition-Metal (Pd, Ni, Mn)-Catalyzed C–C Bond Constructions Involving Unactivated Alkyl Halides and Fundamental Synthetic Building Blocks | Accounts of Chemical Research Transition-Metal (Pd, Ni, Mn)-Catalyzed C–C Bond Constructions Involving Unactivated Alkyl Halides and Fundamental Synthetic Building Blocks | Accounts of Chemical Research](https://pubs.acs.org/cms/10.1021/acs.accounts.9b00044/asset/images/medium/ar-2019-00044e_0002.gif)
Transition-Metal (Pd, Ni, Mn)-Catalyzed C–C Bond Constructions Involving Unactivated Alkyl Halides and Fundamental Synthetic Building Blocks | Accounts of Chemical Research
![Copper-Catalyzed Enantioselective Propargylic Amination of Propargylic Esters with Amines: Copper−Allenylidene Complexes as Key Intermediates | Journal of the American Chemical Society Copper-Catalyzed Enantioselective Propargylic Amination of Propargylic Esters with Amines: Copper−Allenylidene Complexes as Key Intermediates | Journal of the American Chemical Society](https://pubs.acs.org/cms/10.1021/ja1047494/asset/images/medium/ja-2010-047494_0032.gif)
Copper-Catalyzed Enantioselective Propargylic Amination of Propargylic Esters with Amines: Copper−Allenylidene Complexes as Key Intermediates | Journal of the American Chemical Society
Transition-Metal (Pd, Ni, Mn)-Catalyzed C–C Bond Constructions Involving Unactivated Alkyl Halides and Fundamental Synthetic Building Blocks | Accounts of Chemical Research
![Olefin Functionalization/Isomerization Enables Stereoselective Alkene Synthesis. - Abstract - Europe PMC Olefin Functionalization/Isomerization Enables Stereoselective Alkene Synthesis. - Abstract - Europe PMC](https://europepmc.org/articles/PMC9431960/bin/nihms-1768391-t0006.jpg)
Olefin Functionalization/Isomerization Enables Stereoselective Alkene Synthesis. - Abstract - Europe PMC
![Novel 2,3-Dihydro-1,4-Benzoxazines as Potent and Orally Bioavailable Inhibitors of Tumor-Driven Angiogenesis | Journal of Medicinal Chemistry Novel 2,3-Dihydro-1,4-Benzoxazines as Potent and Orally Bioavailable Inhibitors of Tumor-Driven Angiogenesis | Journal of Medicinal Chemistry](https://pubs.acs.org/cms/10.1021/jm701129j/asset/images/medium/jm-2007-01129j_0016.gif)
Novel 2,3-Dihydro-1,4-Benzoxazines as Potent and Orally Bioavailable Inhibitors of Tumor-Driven Angiogenesis | Journal of Medicinal Chemistry
![Covalent Modifiers: A Chemical Perspective on the Reactivity of α,β-Unsaturated Carbonyls with Thiols via Hetero-Michael Addition Reactions | Journal of Medicinal Chemistry Covalent Modifiers: A Chemical Perspective on the Reactivity of α,β-Unsaturated Carbonyls with Thiols via Hetero-Michael Addition Reactions | Journal of Medicinal Chemistry](https://pubs.acs.org/cms/10.1021/acs.jmedchem.6b00788/asset/images/medium/jm-2016-00788x_0081.gif)
Covalent Modifiers: A Chemical Perspective on the Reactivity of α,β-Unsaturated Carbonyls with Thiols via Hetero-Michael Addition Reactions | Journal of Medicinal Chemistry
![Nickel-catalysed migratory hydroalkynylation and enantioselective hydroalkynylation of olefins with bromoalkynes | Nature Communications Nickel-catalysed migratory hydroalkynylation and enantioselective hydroalkynylation of olefins with bromoalkynes | Nature Communications](https://media.springernature.com/m685/springer-static/image/art%3A10.1038%2Fs41467-021-24094-9/MediaObjects/41467_2021_24094_Fig2_HTML.png)
Nickel-catalysed migratory hydroalkynylation and enantioselective hydroalkynylation of olefins with bromoalkynes | Nature Communications
![Iron‐Electrocatalyzed C−H Arylations: Mechanistic Insights into Oxidation‐Induced Reductive Elimination for Ferraelectrocatalysis - Zhu - 2019 - Chemistry – A European Journal - Wiley Online Library Iron‐Electrocatalyzed C−H Arylations: Mechanistic Insights into Oxidation‐Induced Reductive Elimination for Ferraelectrocatalysis - Zhu - 2019 - Chemistry – A European Journal - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/402593a9-fe1b-45a1-8fb3-0ce591882aaa/chem201904018-fig-5003-m.jpg)
Iron‐Electrocatalyzed C−H Arylations: Mechanistic Insights into Oxidation‐Induced Reductive Elimination for Ferraelectrocatalysis - Zhu - 2019 - Chemistry – A European Journal - Wiley Online Library
![Nickel-Catalyzed Reductive Cross-Couplings: New Opportunities for Carbon–Carbon Bond Formations through Photochemistry and Electrochemistry | CCS Chemistry Nickel-Catalyzed Reductive Cross-Couplings: New Opportunities for Carbon–Carbon Bond Formations through Photochemistry and Electrochemistry | CCS Chemistry](https://www.chinesechemsoc.org/cms/asset/f46a5497-61af-4611-ae1d-78a00cff6b9c/sf10.gif)
Nickel-Catalyzed Reductive Cross-Couplings: New Opportunities for Carbon–Carbon Bond Formations through Photochemistry and Electrochemistry | CCS Chemistry
![Structure and therapeutic uses of butyrylcholinesterase: Application in detoxification, Alzheimer's disease, and fat metabolism - Xing - 2021 - Medicinal Research Reviews - Wiley Online Library Structure and therapeutic uses of butyrylcholinesterase: Application in detoxification, Alzheimer's disease, and fat metabolism - Xing - 2021 - Medicinal Research Reviews - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/7801d6e4-2519-4a9a-9e82-8be97c4bbabd/med21745-fig-0010-m.jpg)
Structure and therapeutic uses of butyrylcholinesterase: Application in detoxification, Alzheimer's disease, and fat metabolism - Xing - 2021 - Medicinal Research Reviews - Wiley Online Library
![Recent Strategies for Carbon−Halogen Bond Formation Using Nickel - Marchese - 2021 - Angewandte Chemie - Wiley Online Library Recent Strategies for Carbon−Halogen Bond Formation Using Nickel - Marchese - 2021 - Angewandte Chemie - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/5bf5c066-3404-42de-80a8-473d40663c86/ange202101324-fig-5007-m.jpg)
Recent Strategies for Carbon−Halogen Bond Formation Using Nickel - Marchese - 2021 - Angewandte Chemie - Wiley Online Library
![Development and Mechanistic Studies of (E)-Selective Isomerization/Tandem Hydroarylation Reactions of Alkenes with a Nickel(0)/Phosphine Catalyst | ACS Catalysis Development and Mechanistic Studies of (E)-Selective Isomerization/Tandem Hydroarylation Reactions of Alkenes with a Nickel(0)/Phosphine Catalyst | ACS Catalysis](https://pubs.acs.org/cms/10.1021/acscatal.1c00908/asset/images/medium/cs1c00908_0007.gif)