![Synthesis of Substituted Benzo[b]thiophenes via Sequential One-Pot, Copper-Catalyzed Intermolecular C-S Bond Formation and Palladium-Catalyzed Intramolecular Arene-Alkene Coupling of Bis(het)aryl/alkyl-1,3-monothiodiketones and o-Bromoiodoarenes ... Synthesis of Substituted Benzo[b]thiophenes via Sequential One-Pot, Copper-Catalyzed Intermolecular C-S Bond Formation and Palladium-Catalyzed Intramolecular Arene-Alkene Coupling of Bis(het)aryl/alkyl-1,3-monothiodiketones and o-Bromoiodoarenes ...](https://d3i71xaburhd42.cloudfront.net/95cff7feec2fffaff4d5ae744c1d00c294992095/2-Table1-1.png)
Synthesis of Substituted Benzo[b]thiophenes via Sequential One-Pot, Copper-Catalyzed Intermolecular C-S Bond Formation and Palladium-Catalyzed Intramolecular Arene-Alkene Coupling of Bis(het)aryl/alkyl-1,3-monothiodiketones and o-Bromoiodoarenes ...
![A Cooperative Strategy for the Highly Selective Intermolecular Oxycarbonylation Reaction of Alkenes using a Palladium Catalyst - Angew. Chem. Int. Ed. - X-MOL A Cooperative Strategy for the Highly Selective Intermolecular Oxycarbonylation Reaction of Alkenes using a Palladium Catalyst - Angew. Chem. Int. Ed. - X-MOL](https://xpic.x-mol.com/paperImg%2F2020_03_12%2FAngewandte_Chemie_International_Edition_All_img%2F10.1002_anie.201607248.jpg)
A Cooperative Strategy for the Highly Selective Intermolecular Oxycarbonylation Reaction of Alkenes using a Palladium Catalyst - Angew. Chem. Int. Ed. - X-MOL
![Catalysts | Free Full-Text | Palladium and Copper Catalyzed Sonogashira cross Coupling an Excellent Methodology for C-C Bond Formation over 17 Years: A Review | HTML Catalysts | Free Full-Text | Palladium and Copper Catalyzed Sonogashira cross Coupling an Excellent Methodology for C-C Bond Formation over 17 Years: A Review | HTML](https://www.mdpi.com/catalysts/catalysts-10-00443/article_deploy/html/images/catalysts-10-00443-sch012.png)
Catalysts | Free Full-Text | Palladium and Copper Catalyzed Sonogashira cross Coupling an Excellent Methodology for C-C Bond Formation over 17 Years: A Review | HTML
![Quadruple C-H activation coupled to hydrofunctionalization and C-H silylation/borylation enabled by weakly coordinated palladium catalyst | Nature Communications Quadruple C-H activation coupled to hydrofunctionalization and C-H silylation/borylation enabled by weakly coordinated palladium catalyst | Nature Communications](https://media.springernature.com/m685/springer-static/image/art%3A10.1038%2Fs41467-020-19508-z/MediaObjects/41467_2020_19508_Fig1_HTML.png)
Quadruple C-H activation coupled to hydrofunctionalization and C-H silylation/borylation enabled by weakly coordinated palladium catalyst | Nature Communications
![Expeditious Synthesis of Tetrasubstituted Helical Alkenes by a Cascade of Palladium‐Catalyzed CH Activations - Liu - 2012 - Angewandte Chemie International Edition - Wiley Online Library Expeditious Synthesis of Tetrasubstituted Helical Alkenes by a Cascade of Palladium‐Catalyzed CH Activations - Liu - 2012 - Angewandte Chemie International Edition - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/95262512-2a6a-4659-9407-f595485d3f2e/mcontent.jpg)
Expeditious Synthesis of Tetrasubstituted Helical Alkenes by a Cascade of Palladium‐Catalyzed CH Activations - Liu - 2012 - Angewandte Chemie International Edition - Wiley Online Library
![a) The change in fluorescence intensity of compound 1 with incremental... | Download Scientific Diagram a) The change in fluorescence intensity of compound 1 with incremental... | Download Scientific Diagram](https://www.researchgate.net/profile/Soumava_Biswas/publication/273124943/figure/fig1/AS:391856530706477@1470437285578/a-The-change-in-fluorescence-intensity-of-compound-1-with-incremental-addition-of-Pd-2.png)
a) The change in fluorescence intensity of compound 1 with incremental... | Download Scientific Diagram
![Scheme 1 Reactions used to demonstrate the catalytic farming concept.... | Download Scientific Diagram Scheme 1 Reactions used to demonstrate the catalytic farming concept.... | Download Scientific Diagram](https://www.researchgate.net/publication/328966802/figure/fig1/AS:743717463916544@1554327469203/Scheme-1-Reactions-used-to-demonstrate-the-catalytic-farming-concept-A-Sonogashira_Q640.jpg)
Scheme 1 Reactions used to demonstrate the catalytic farming concept.... | Download Scientific Diagram
![N-alkylation of 2-pyridone derivatives via palladium(II)-catalyzed directed alkene hydroamination - ScienceDirect N-alkylation of 2-pyridone derivatives via palladium(II)-catalyzed directed alkene hydroamination - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0040402017303605-fx1.jpg)
N-alkylation of 2-pyridone derivatives via palladium(II)-catalyzed directed alkene hydroamination - ScienceDirect
![PDF) Pd/P( t -Bu) 3 : A Mild Catalyst for Selective Reduction of Alkenes under Transfer-Hydrogenation Conditions PDF) Pd/P( t -Bu) 3 : A Mild Catalyst for Selective Reduction of Alkenes under Transfer-Hydrogenation Conditions](https://www.researchgate.net/profile/Jean_Brunel/publication/232613512/figure/tbl1/AS:669310318034945@1536587423066/Influence-of-the-nature-of-the-palladium-source-on-the-Pd-catalyzed-reduction-of_Q320.jpg)
PDF) Pd/P( t -Bu) 3 : A Mild Catalyst for Selective Reduction of Alkenes under Transfer-Hydrogenation Conditions
Highly selective fluorescent probe for detection and visualization of palladium ions in mixed aqueous media - RSC Advances (RSC Publishing)
![Molecules | Free Full-Text | Asymmetric Palladium-Catalysed Intramolecular Wacker-Type Cyclisations of Unsaturated Alcohols and Amino Alcohols | HTML Molecules | Free Full-Text | Asymmetric Palladium-Catalysed Intramolecular Wacker-Type Cyclisations of Unsaturated Alcohols and Amino Alcohols | HTML](https://www.mdpi.com/molecules/molecules-18-06173/article_deploy/html/images/molecules-18-06173-g021.png)
Molecules | Free Full-Text | Asymmetric Palladium-Catalysed Intramolecular Wacker-Type Cyclisations of Unsaturated Alcohols and Amino Alcohols | HTML
![Highly selective electrochemical hydrogenation of alkynes: Rapid construction of mechanochromic materials | Science Advances Highly selective electrochemical hydrogenation of alkynes: Rapid construction of mechanochromic materials | Science Advances](https://advances.sciencemag.org/content/5/5/eaaw2774/F1.large.jpg)
Highly selective electrochemical hydrogenation of alkynes: Rapid construction of mechanochromic materials | Science Advances
![Phosphaannulation of Aryl‐ and Benzylphosphonic Acids with Unactivated Alkenes via Palladium‐Catalyzed CH Activation/Oxidative Cyclization Reaction - Jeon - 2015 - Advanced Synthesis & Catalysis - Wiley Online Library Phosphaannulation of Aryl‐ and Benzylphosphonic Acids with Unactivated Alkenes via Palladium‐Catalyzed CH Activation/Oxidative Cyclization Reaction - Jeon - 2015 - Advanced Synthesis & Catalysis - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/b9a4492a-f75a-4fa8-8f77-2b5fd9cedab9/mcontent.jpg)
Phosphaannulation of Aryl‐ and Benzylphosphonic Acids with Unactivated Alkenes via Palladium‐Catalyzed CH Activation/Oxidative Cyclization Reaction - Jeon - 2015 - Advanced Synthesis & Catalysis - Wiley Online Library
Palladium nanoparticles supported on ionic liquid modified, magnetic nanobeads – recyclable, high-capacity catalysts for alkene hydrogenation - RSC Advances (RSC Publishing)
Graphdiyne-based Pd single-atom catalyst for semihydrogenation of alkynes to alkenes with high selectivity and conversion under mild conditions - Journal of Materials Chemistry A (RSC Publishing)
![Organophotoredox/palladium dual catalytic decarboxylative Csp 3 –Csp 3 coupling of carboxylic acids and π-electrophiles - Chemical Science (RSC Publishing) DOI:10.1039/D0SC02609C Organophotoredox/palladium dual catalytic decarboxylative Csp 3 –Csp 3 coupling of carboxylic acids and π-electrophiles - Chemical Science (RSC Publishing) DOI:10.1039/D0SC02609C](https://pubs.rsc.org/image/article/2020/SC/d0sc02609c/d0sc02609c-s1_hi-res.gif)
Organophotoredox/palladium dual catalytic decarboxylative Csp 3 –Csp 3 coupling of carboxylic acids and π-electrophiles - Chemical Science (RSC Publishing) DOI:10.1039/D0SC02609C
![Photoredox-catalyzed branch-selective pyridylation of alkenes for the expedient synthesis of Triprolidine | Nature Communications Photoredox-catalyzed branch-selective pyridylation of alkenes for the expedient synthesis of Triprolidine | Nature Communications](https://media.springernature.com/m685/springer-static/image/art%3A10.1038%2Fs41467-019-08669-1/MediaObjects/41467_2019_8669_Fig1_HTML.png)
Photoredox-catalyzed branch-selective pyridylation of alkenes for the expedient synthesis of Triprolidine | Nature Communications
![Scheme 1 Synthesis of TTZ-1 and schematic of its fluorescent response... | Download Scientific Diagram Scheme 1 Synthesis of TTZ-1 and schematic of its fluorescent response... | Download Scientific Diagram](https://www.researchgate.net/profile/Zhigang_Xie2/publication/257068579/figure/fig2/AS:669278151909386@1536579754808/Scheme-1-Synthesis-of-TTZ-1-and-schematic-of-its-fluorescent-response-to-alkene_Q640.jpg)
Scheme 1 Synthesis of TTZ-1 and schematic of its fluorescent response... | Download Scientific Diagram
![Synthesis of (1 E ,3 E )-1,4-diarylbuta-1,3-dienes promoted by μ-OMs palladium–dimer complex | SpringerLink Synthesis of (1 E ,3 E )-1,4-diarylbuta-1,3-dienes promoted by μ-OMs palladium–dimer complex | SpringerLink](https://media.springernature.com/lw685/springer-static/image/art%3A10.1186%2Fs13065-019-0561-3/MediaObjects/13065_2019_561_Fig3_HTML.png)
Synthesis of (1 E ,3 E )-1,4-diarylbuta-1,3-dienes promoted by μ-OMs palladium–dimer complex | SpringerLink
![Recent Developments in Pd0‐Catalyzed Alkene‐Carboheterofunctionalization Reactions - Garlets - 2017 - Asian Journal of Organic Chemistry - Wiley Online Library Recent Developments in Pd0‐Catalyzed Alkene‐Carboheterofunctionalization Reactions - Garlets - 2017 - Asian Journal of Organic Chemistry - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/bf546ea1-83a1-46dc-8f4f-9933ec203f0d/ajoc201600577-fig-5003-m.jpg)