![Diastereoconvergent Negishi cross-coupling using functionalized cyclohexylzinc reagents. | Semantic Scholar Diastereoconvergent Negishi cross-coupling using functionalized cyclohexylzinc reagents. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/29aeec2b51dd6f757f414790205578d03eea983c/2-Table1-1.png)
Diastereoconvergent Negishi cross-coupling using functionalized cyclohexylzinc reagents. | Semantic Scholar
![Electroreductive Nickel‐Catalyzed Thiolation: Efficient Cross‐Electrophile Coupling for C−S Formation - Ang - 2021 - Chemistry – A European Journal - Wiley Online Library Electroreductive Nickel‐Catalyzed Thiolation: Efficient Cross‐Electrophile Coupling for C−S Formation - Ang - 2021 - Chemistry – A European Journal - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/bcc3b9b6-e881-4e04-af62-325201bd28f4/chem202005449-fig-5001-m.jpg)
Electroreductive Nickel‐Catalyzed Thiolation: Efficient Cross‐Electrophile Coupling for C−S Formation - Ang - 2021 - Chemistry – A European Journal - Wiley Online Library
![Metalated nitriles : N- and C-coordination preferences of Li, Mg, and Cu cations - Chemical Communications (RSC Publishing) DOI:10.1039/C3CC41703D Metalated nitriles : N- and C-coordination preferences of Li, Mg, and Cu cations - Chemical Communications (RSC Publishing) DOI:10.1039/C3CC41703D](https://pubs.rsc.org/image/article/2013/CC/c3cc41703d/c3cc41703d-f1.gif)
Metalated nitriles : N- and C-coordination preferences of Li, Mg, and Cu cations - Chemical Communications (RSC Publishing) DOI:10.1039/C3CC41703D
![Nickel-catalyzed reductive thiolation and selenylation of unactivated alkyl bromides | Nature Communications Nickel-catalyzed reductive thiolation and selenylation of unactivated alkyl bromides | Nature Communications](https://media.springernature.com/full/springer-static/image/art%3A10.1038%2Fs41467-018-04646-2/MediaObjects/41467_2018_4646_Fig1_HTML.jpg)
Nickel-catalyzed reductive thiolation and selenylation of unactivated alkyl bromides | Nature Communications
![Electroreductive Nickel‐Catalyzed Thiolation: Efficient Cross‐Electrophile Coupling for C−S Formation - Ang - 2021 - Chemistry – A European Journal - Wiley Online Library Electroreductive Nickel‐Catalyzed Thiolation: Efficient Cross‐Electrophile Coupling for C−S Formation - Ang - 2021 - Chemistry – A European Journal - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/5eedd231-47c4-416c-b0cb-fe0631e0cf4e/chem202005449-fig-5005-m.jpg)
Electroreductive Nickel‐Catalyzed Thiolation: Efficient Cross‐Electrophile Coupling for C−S Formation - Ang - 2021 - Chemistry – A European Journal - Wiley Online Library
![Johannes HEPPEKAUSEN | PhD | Max Planck Institute for Coal Research, Mülheim | KOFO | Department of Metalorganic Chemistry Johannes HEPPEKAUSEN | PhD | Max Planck Institute for Coal Research, Mülheim | KOFO | Department of Metalorganic Chemistry](https://www.researchgate.net/profile/Johannes-Heppekausen-2/publication/244560123/figure/fig1/AS:669081661345826@1536532907902/Aryl-halides-a-X-Br-b-X-I-and-resulting-ring-systems-from-palladium-catalyzed_Q320.jpg)