![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_0020.gif)
Transition-Metal (Pd, Ni, Mn)-Catalyzed C–C Bond Constructions Involving Unactivated Alkyl Halides and Fundamental Synthetic Building Blocks | Accounts of Chemical Research
![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
![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
![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
![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
![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
![Covalent Modifiers: A Chemical Perspective on the Reactivity of α,β-Unsaturated Carbonyls with Thiols via Hetero-Michael Addition Reactions. - Abstract - Europe PMC Covalent Modifiers: A Chemical Perspective on the Reactivity of α,β-Unsaturated Carbonyls with Thiols via Hetero-Michael Addition Reactions. - Abstract - Europe PMC](https://europepmc.org/articles/PMC5308545/bin/nihms-848842-f0110.jpg)
Covalent Modifiers: A Chemical Perspective on the Reactivity of α,β-Unsaturated Carbonyls with Thiols via Hetero-Michael Addition Reactions. - Abstract - Europe PMC
Transition-Metal (Pd, Ni, Mn)-Catalyzed C–C Bond Constructions Involving Unactivated Alkyl Halides and Fundamental Synthetic Building Blocks | Accounts of Chemical Research
![Facile Synthesis of Chiral Arylamines, Alkylamines and Amides by Enantioselective NiH‐Catalyzed Hydroamination - Meng - 2021 - Angewandte Chemie International Edition - Wiley Online Library Facile Synthesis of Chiral Arylamines, Alkylamines and Amides by Enantioselective NiH‐Catalyzed Hydroamination - Meng - 2021 - Angewandte Chemie International Edition - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/878be16b-5a3b-48a1-aa95-1e8a9f3e6319/anie202109881-gra-0004.png)
Facile Synthesis of Chiral Arylamines, Alkylamines and Amides by Enantioselective NiH‐Catalyzed Hydroamination - Meng - 2021 - Angewandte Chemie International Edition - 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_0011.gif)
Development and Mechanistic Studies of (E)-Selective Isomerization/Tandem Hydroarylation Reactions of Alkenes with a Nickel(0)/Phosphine Catalyst | ACS Catalysis
![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
![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)