![Axially Chiral Cyclic Diphosphine Ligand-Enabled Palladium-Catalyzed Intramolecular Asymmetric Hydroarylation - ScienceDirect Axially Chiral Cyclic Diphosphine Ligand-Enabled Palladium-Catalyzed Intramolecular Asymmetric Hydroarylation - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S2589004218302086-fx1.jpg)
Axially Chiral Cyclic Diphosphine Ligand-Enabled Palladium-Catalyzed Intramolecular Asymmetric Hydroarylation - ScienceDirect
![Functionalized nitrogen ligands (CN) for palladium catalyzed cross-coupling reactions (part II) - ScienceDirect Functionalized nitrogen ligands (CN) for palladium catalyzed cross-coupling reactions (part II) - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0022328X18308374-gr2.jpg)
Functionalized nitrogen ligands (CN) for palladium catalyzed cross-coupling reactions (part II) - ScienceDirect
Water soluble palladium(ii) and platinum(ii) acyclic diaminocarbene complexes: solution behavior, DNA binding, and antiproliferative activity - New Journal of Chemistry (RSC Publishing)
![Cationic Two-Coordinate Complexes of Pd(I) and Pt(I) Have Longer Metal- Ligand Bonds Than Their Neutral Counterparts - ScienceDirect Cationic Two-Coordinate Complexes of Pd(I) and Pt(I) Have Longer Metal- Ligand Bonds Than Their Neutral Counterparts - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S2451929416302340-fx1.jpg)
Cationic Two-Coordinate Complexes of Pd(I) and Pt(I) Have Longer Metal- Ligand Bonds Than Their Neutral Counterparts - ScienceDirect
![Flexible, N-sulfonyl-substituted aliphatic amine ligands in palladium-catalyzed Suzuki–Miyaura CC coupling: Influence of substituents bulkiness and co- ligand size - ScienceDirect Flexible, N-sulfonyl-substituted aliphatic amine ligands in palladium-catalyzed Suzuki–Miyaura CC coupling: Influence of substituents bulkiness and co- ligand size - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0277538718307691-ga1.jpg)
Flexible, N-sulfonyl-substituted aliphatic amine ligands in palladium-catalyzed Suzuki–Miyaura CC coupling: Influence of substituents bulkiness and co- ligand size - ScienceDirect
![Ligand-enabled C(sp 3 )-H activation a, C-H activation of aliphatic... | Download Scientific Diagram Ligand-enabled C(sp 3 )-H activation a, C-H activation of aliphatic... | Download Scientific Diagram](https://www.researchgate.net/profile/Jin-Quan_Yu/publication/259876411/figure/fig3/AS:667045066702848@1536047345033/Ligand-enabled-Csp-3-H-activation-a-C-H-activation-of-aliphatic-amines-directed-by.jpg)
Ligand-enabled C(sp 3 )-H activation a, C-H activation of aliphatic... | Download Scientific Diagram
![Palladium-catalyzed C–H activation of anisole with electron-deficient auxiliary ligands: a mechanistic investigation - Organic & Biomolecular Chemistry (RSC Publishing) Palladium-catalyzed C–H activation of anisole with electron-deficient auxiliary ligands: a mechanistic investigation - Organic & Biomolecular Chemistry (RSC Publishing)](https://pubs.rsc.org/image/article/2020/ob/d0ob01133a/d0ob01133a-s1_hi-res.gif)
Palladium-catalyzed C–H activation of anisole with electron-deficient auxiliary ligands: a mechanistic investigation - Organic & Biomolecular Chemistry (RSC Publishing)
![Ligand‐Assisted Palladium(II)/(IV) Oxidation for sp3 CH Fluorination - Sun - 2016 - Advanced Synthesis & Catalysis - Wiley Online Library Ligand‐Assisted Palladium(II)/(IV) Oxidation for sp3 CH Fluorination - Sun - 2016 - Advanced Synthesis & Catalysis - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/56d726e9-3d17-4897-a12c-82b5823321eb/mcontent.jpg)
Ligand‐Assisted Palladium(II)/(IV) Oxidation for sp3 CH Fluorination - Sun - 2016 - Advanced Synthesis & Catalysis - Wiley Online Library
![Olefin Dimerization and Isomerization Catalyzed by Pyridylidene Amide Palladium Complexes - Organometallics - X-MOL Olefin Dimerization and Isomerization Catalyzed by Pyridylidene Amide Palladium Complexes - Organometallics - X-MOL](https://xpic.x-mol.com/20180925%2F10.1021_acs.organomet.8b00422.jpg)
Olefin Dimerization and Isomerization Catalyzed by Pyridylidene Amide Palladium Complexes - Organometallics - X-MOL
![2,2′-Bipyridin]-6(1H)-one, a Truly Cooperating Ligand in the Palladium-Mediated C–H Activation Step: Experimental Evidence in the Direct C-3 Arylation of Pyridine - J. Am. Chem. Soc. - X-MOL 2,2′-Bipyridin]-6(1H)-one, a Truly Cooperating Ligand in the Palladium-Mediated C–H Activation Step: Experimental Evidence in the Direct C-3 Arylation of Pyridine - J. Am. Chem. Soc. - X-MOL](https://xpic.x-mol.com/paperImg%2F2020_03_12%2FJournal_of_the_American_Chemical_Society_All_img%2F10.1021_jacs.8b10680.gif)
2,2′-Bipyridin]-6(1H)-one, a Truly Cooperating Ligand in the Palladium-Mediated C–H Activation Step: Experimental Evidence in the Direct C-3 Arylation of Pyridine - J. Am. Chem. Soc. - X-MOL
![Iodide-enhanced palladium catalysis via formation of iodide-bridged binuclear palladium complex | Communications Chemistry Iodide-enhanced palladium catalysis via formation of iodide-bridged binuclear palladium complex | Communications Chemistry](https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fs42004-020-0287-0/MediaObjects/42004_2020_287_Fig2_HTML.png)
Iodide-enhanced palladium catalysis via formation of iodide-bridged binuclear palladium complex | Communications Chemistry
Neutral, cationic and anionic organonickel and -palladium complexes supported by iminophosphine/phosphinoenaminato ligands - Dalton Transactions (RSC Publishing)
A study of the platinum (II), palladium (II), and rhodium (III) chelates of aspartic and glutamic acid
![N-Heterocyclic carbene (NHC) ligands and palladium in homogeneous cross-coupling catalysis: a perfect union - Chemical Society Reviews (RSC Publishing) N-Heterocyclic carbene (NHC) ligands and palladium in homogeneous cross-coupling catalysis: a perfect union - Chemical Society Reviews (RSC Publishing)](https://pubs.rsc.org/image/article/2011/cs/c1cs15088j/c1cs15088j-f2.gif)
N-Heterocyclic carbene (NHC) ligands and palladium in homogeneous cross-coupling catalysis: a perfect union - Chemical Society Reviews (RSC Publishing)
![Iodide-enhanced palladium catalysis via formation of iodide-bridged binuclear palladium complex | Communications Chemistry Iodide-enhanced palladium catalysis via formation of iodide-bridged binuclear palladium complex | Communications Chemistry](https://media.springernature.com/m685/springer-static/image/art%3A10.1038%2Fs42004-020-0287-0/MediaObjects/42004_2020_287_Fig1_HTML.png)
Iodide-enhanced palladium catalysis via formation of iodide-bridged binuclear palladium complex | Communications Chemistry
![Ligand‐Controlled Palladium‐Catalyzed Pyridylation of 1‐tert‐Butoxycarbonyl‐3‐iodoazetidine: Regioselective Synthesis of 2‐ and 3‐Heteroarylazetidines - Zhang - 2017 - Advanced Synthesis & Catalysis - Wiley Online Library Ligand‐Controlled Palladium‐Catalyzed Pyridylation of 1‐tert‐Butoxycarbonyl‐3‐iodoazetidine: Regioselective Synthesis of 2‐ and 3‐Heteroarylazetidines - Zhang - 2017 - Advanced Synthesis & Catalysis - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/914811b6-5d77-4201-be75-904508289314/adsc201600470-toc-0001-m.jpg)