![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
![Nickel/Brønsted acid dual-catalyzed regio- and enantioselective hydrophosphinylation of 1,3-dienes: access to chiral allylic phosphine oxides - Chemical Science (RSC Publishing) DOI:10.1039/D1SC05651D Nickel/Brønsted acid dual-catalyzed regio- and enantioselective hydrophosphinylation of 1,3-dienes: access to chiral allylic phosphine oxides - Chemical Science (RSC Publishing) DOI:10.1039/D1SC05651D](https://pubs.rsc.org/image/article/2022/SC/d1sc05651d/d1sc05651d-f4_hi-res.gif)
Nickel/Brønsted acid dual-catalyzed regio- and enantioselective hydrophosphinylation of 1,3-dienes: access to chiral allylic phosphine oxides - Chemical Science (RSC Publishing) DOI:10.1039/D1SC05651D
![Facile Synthesis of Chiral Arylamines, Alkylamines and Amides by Enantioselective NiH‐Catalyzed Hydroamination - Meng - 2021 - Angewandte Chemie - Wiley Online Library Facile Synthesis of Chiral Arylamines, Alkylamines and Amides by Enantioselective NiH‐Catalyzed Hydroamination - Meng - 2021 - Angewandte Chemie - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/8d5f6788-4cd1-4f4e-97cc-b380fd4286ae/ange202109881-gra-0004.png)
Facile Synthesis of Chiral Arylamines, Alkylamines and Amides by Enantioselective NiH‐Catalyzed Hydroamination - Meng - 2021 - Angewandte Chemie - Wiley Online Library
![Regio- and enantioselective remote hydroarylation using a ligand-relay strategy | Nature Communications Regio- and enantioselective remote hydroarylation using a ligand-relay strategy | Nature Communications](https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fs41467-022-30006-2/MediaObjects/41467_2022_30006_Fig3_HTML.png)
Regio- and enantioselective remote hydroarylation using a ligand-relay strategy | Nature Communications
![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/large/cs1c00908_0005.jpeg)
Development and Mechanistic Studies of (E)-Selective Isomerization/Tandem Hydroarylation Reactions of Alkenes with a Nickel(0)/Phosphine Catalyst | ACS Catalysis
![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/lw685/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
![18 Supramolecular coordination chemistry - Annual Reports Section 18 Supramolecular coordination chemistry - Annual Reports Section](https://pubs.rsc.org/image/article/2001/IC/b102906c/b102906c-u1.gif)
18 Supramolecular coordination chemistry - Annual Reports Section "A" (Inorganic Chemistry) (RSC Publishing) DOI:10.1039/B102906C
![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-f0003.jpg)
Covalent Modifiers: A Chemical Perspective on the Reactivity of α,β-Unsaturated Carbonyls with Thiols via Hetero-Michael Addition Reactions. - Abstract - Europe PMC
![18 Supramolecular coordination chemistry - Annual Reports Section 18 Supramolecular coordination chemistry - Annual Reports Section](https://pubs.rsc.org/image/article/2001/IC/b102906c/b102906c-u19.gif)
18 Supramolecular coordination chemistry - Annual Reports Section "A" (Inorganic Chemistry) (RSC Publishing) DOI:10.1039/B102906C
![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/large/ja-2010-047494_0016.jpeg)
Copper-Catalyzed Enantioselective Propargylic Amination of Propargylic Esters with Amines: Copper−Allenylidene Complexes as Key Intermediates | Journal of the American Chemical Society
![A biomimetic S<sub>H</sub>2 cross-coupling mechanism for quaternary sp<sup>3</sup>-carbon formation. - Abstract - Europe PMC A biomimetic S<sub>H</sub>2 cross-coupling mechanism for quaternary sp<sup>3</sup>-carbon formation. - Abstract - Europe PMC](https://europepmc.org/articles/PMC8926084/bin/nihms-1756096-f0003.jpg)
A biomimetic SH2 cross-coupling mechanism for quaternary sp3-carbon formation. - Abstract - Europe PMC
![C2-ketonylation of carbohydrates via excited-state palladium-catalyzed 1,2-spin-center shift - Chemical Science (RSC Publishing) DOI:10.1039/D2SC01042A C2-ketonylation of carbohydrates via excited-state palladium-catalyzed 1,2-spin-center shift - Chemical Science (RSC Publishing) DOI:10.1039/D2SC01042A](https://pubs.rsc.org/image/article/2022/SC/d2sc01042a/d2sc01042a-u2_hi-res.gif)
C2-ketonylation of carbohydrates via excited-state palladium-catalyzed 1,2-spin-center shift - Chemical Science (RSC Publishing) DOI:10.1039/D2SC01042A
![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
![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/991bf37a-23c5-419f-a9ae-ac10e1512e04/anie202109881-fig-5001-m.jpg)
Facile Synthesis of Chiral Arylamines, Alkylamines and Amides by Enantioselective NiH‐Catalyzed Hydroamination - Meng - 2021 - Angewandte Chemie International Edition - 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 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/40795051-e817-43aa-b3b1-57cd7297abeb/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-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/full/springer-static/image/art%3A10.1038%2Fs41467-021-24094-9/MediaObjects/41467_2021_24094_Fig1_HTML.png)
Nickel-catalysed migratory hydroalkynylation and enantioselective hydroalkynylation of olefins with bromoalkynes | Nature Communications
![Nickel-catalysed migratory hydroalkynylation and enantioselective hydroalkynylation of olefins with bromoalkynes. - Abstract - Europe PMC Nickel-catalysed migratory hydroalkynylation and enantioselective hydroalkynylation of olefins with bromoalkynes. - Abstract - Europe PMC](https://europepmc.org/articles/PMC8213830/bin/41467_2021_24094_Fig3_HTML.jpg)
Nickel-catalysed migratory hydroalkynylation and enantioselective hydroalkynylation of olefins with bromoalkynes. - Abstract - Europe PMC
![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/d1c713a9-9034-46e0-a4cf-c64b31b44f4d/anie202109881-gra-0005.png)
Facile Synthesis of Chiral Arylamines, Alkylamines and Amides by Enantioselective NiH‐Catalyzed Hydroamination - Meng - 2021 - Angewandte Chemie International Edition - Wiley Online Library
![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/lw685/springer-static/image/art%3A10.1038%2Fs41467-021-24094-9/MediaObjects/41467_2021_24094_Fig4_HTML.png)