![From Bis(silylene) and Bis(germylene) Pincer-Type Nickel(II) Complexes to Isolable Intermediates of the Nickel-Catalyzed Sonogashira Cross-Coupling Reaction | The Hartwig Group From Bis(silylene) and Bis(germylene) Pincer-Type Nickel(II) Complexes to Isolable Intermediates of the Nickel-Catalyzed Sonogashira Cross-Coupling Reaction | The Hartwig Group](https://hartwig.cchem.berkeley.edu/static/img/pubs/toc_303.jpg)
From Bis(silylene) and Bis(germylene) Pincer-Type Nickel(II) Complexes to Isolable Intermediates of the Nickel-Catalyzed Sonogashira Cross-Coupling Reaction | The Hartwig Group
![Catalysts | Free Full-Text | Acyl Sonogashira Cross-Coupling: State of the Art and Application to the Synthesis of Heterocyclic Compounds | HTML Catalysts | Free Full-Text | Acyl Sonogashira Cross-Coupling: State of the Art and Application to the Synthesis of Heterocyclic Compounds | HTML](https://www.mdpi.com/catalysts/catalysts-10-00025/article_deploy/html/images/catalysts-10-00025-sch025.png)
Catalysts | Free Full-Text | Acyl Sonogashira Cross-Coupling: State of the Art and Application to the Synthesis of Heterocyclic Compounds | HTML
![Recent mechanistic developments and next generation catalysts for the Sonogashira coupling reaction - RSC Advances (RSC Publishing) DOI:10.1039/C4RA09105A Recent mechanistic developments and next generation catalysts for the Sonogashira coupling reaction - RSC Advances (RSC Publishing) DOI:10.1039/C4RA09105A](https://pubs.rsc.org/image/article/2014/RA/c4ra09105a/c4ra09105a-f1_hi-res.gif)
Recent mechanistic developments and next generation catalysts for the Sonogashira coupling reaction - RSC Advances (RSC Publishing) DOI:10.1039/C4RA09105A
![Insights into Sonogashira Cross‐Coupling by High‐Throughput Kinetics and Descriptor Modeling - an der Heiden - 2008 - Chemistry – A European Journal - Wiley Online Library Insights into Sonogashira Cross‐Coupling by High‐Throughput Kinetics and Descriptor Modeling - an der Heiden - 2008 - Chemistry – A European Journal - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/0dd7bc2d-b3b2-4781-982f-ca6bbbd5d32e/mfig001.gif)
Insights into Sonogashira Cross‐Coupling by High‐Throughput Kinetics and Descriptor Modeling - an der Heiden - 2008 - Chemistry – A European Journal - Wiley Online Library
![Mechanism of copper-free Sonogashira reaction operates through palladium-palladium transmetallation | Nature Communications Mechanism of copper-free Sonogashira reaction operates through palladium-palladium transmetallation | Nature Communications](https://media.springernature.com/m685/springer-static/image/art%3A10.1038%2Fs41467-018-07081-5/MediaObjects/41467_2018_7081_Fig1_HTML.png)
Mechanism of copper-free Sonogashira reaction operates through palladium-palladium transmetallation | Nature Communications
![Mechanism of copper-free Sonogashira reaction operates through palladium-palladium transmetallation | Nature Communications Mechanism of copper-free Sonogashira reaction operates through palladium-palladium transmetallation | Nature Communications](https://media.springernature.com/full/springer-static/image/art%3A10.1038%2Fs41467-018-07081-5/MediaObjects/41467_2018_7081_Fig1_HTML.png)
Mechanism of copper-free Sonogashira reaction operates through palladium-palladium transmetallation | Nature Communications
![Catalysts | Free Full-Text | Microwave-Assisted Palladium-Catalyzed Cross- Coupling Reactions: Generation of Carbon–Carbon Bond | HTML Catalysts | Free Full-Text | Microwave-Assisted Palladium-Catalyzed Cross- Coupling Reactions: Generation of Carbon–Carbon Bond | HTML](https://www.mdpi.com/catalysts/catalysts-10-00004/article_deploy/html/images/catalysts-10-00004-sch011-550.jpg)
Catalysts | Free Full-Text | Microwave-Assisted Palladium-Catalyzed Cross- Coupling Reactions: Generation of Carbon–Carbon Bond | HTML
![Copper-catalyzed enantioselective Sonogashira-type oxidative cross-coupling of unactivated C(sp3)−H bonds with alkynes | Nature Communications Copper-catalyzed enantioselective Sonogashira-type oxidative cross-coupling of unactivated C(sp3)−H bonds with alkynes | Nature Communications](https://media.springernature.com/full/springer-static/image/art%3A10.1038%2Fs41467-019-13705-1/MediaObjects/41467_2019_13705_Fig1_HTML.png)
Copper-catalyzed enantioselective Sonogashira-type oxidative cross-coupling of unactivated C(sp3)−H bonds with alkynes | Nature Communications
![The Sonogashira reaction. a General representation of Pd/Cu catalysed... | Download Scientific Diagram The Sonogashira reaction. a General representation of Pd/Cu catalysed... | Download Scientific Diagram](https://www.researchgate.net/publication/328999016/figure/fig3/AS:958953110401024@1605643646077/The-Sonogashira-reaction-a-General-representation-of-Pd-Cu-catalysed-and-Cu-free.png)
The Sonogashira reaction. a General representation of Pd/Cu catalysed... | Download Scientific Diagram
![img src="/img/revistas/jsaimm/v117n10/AAA.jpg" align="absmiddle">: a copper- and ligand-free quasi-heterogeneous catalyst for aquacatalytic Sonogashira cross-coupling reaction img src="/img/revistas/jsaimm/v117n10/AAA.jpg" align="absmiddle">: a copper- and ligand-free quasi-heterogeneous catalyst for aquacatalytic Sonogashira cross-coupling reaction](http://www.scielo.org.za/img/revistas/jsaimm/v117n10/07f03.jpg)