![NHC-palladium chloride-imidazole[NHC-Pd(II)-Im]complexes|1314876-23-7——Nanjing Finetech Chemical Co., Ltd.](http://www.fine-chemtech.com/Uploads/5837a4c45b105.png "NHC-palladium chloride-imidazole[NHC-Pd(II)-Im]complexes|1314876-23-7——Nanjing Finetech Chemical Co., Ltd.")
NHC-palladium chloride-imidazole[NHC-Pd(II)-Im]complexes|1314876-23-7——Nanjing Finetech Chemical Co., Ltd.
Air-stable imidazole-imine palladium complexes for Suzuki–Miyaura coupling: Toward an efficient, green synthesis of biaryl compounds - ScienceDirect
Palladium(2+) (3-ethenidyl-1,1,3,3-tetramethyldisiloxanyl)ethenide - 1,3-dimesityl-2,3-dihydro-1H-imidazole (1:1:1) | C29H42N2OPdSi2 | ChemSpider
The palladium-imidazole complexes I-V used in these studies. | Download Scientific Diagram
Structure, dynamics and catalytic activity of palladium(II) complexes with imidazole ligands - ScienceDirect
Palladium Catalyst for the Synthesis of 2,4,5-Trisubstituted Imidazoles | TCI EUROPE N.V.
![C(sp2)-H Functionalization of Imidazole at the C2- and C4-Position via Palladium-Catalyzed Isocyanide Insertion Leading to Indeno[1,2-d]imidazole and Imidazo[1,2-a]indole Derivatives.,The Journal of Organic Chemistry - X-MOL](https://xpic.x-mol.com/20200822%2F10.1021_acs.joc.0c01454.gif "C(sp2)-H Functionalization of Imidazole at the C2- and C4-Position via Palladium-Catalyzed Isocyanide Insertion Leading to Indeno[1,2-d]imidazole and Imidazo[1,2-a]indole Derivatives.,The Journal of Organic Chemistry - X-MOL")
C(sp2)-H Functionalization of Imidazole at the C2- and C4-Position via Palladium-Catalyzed Isocyanide Insertion Leading to Indeno[1,2-d]imidazole and Imidazo[1,2-a]indole Derivatives.,The Journal of Organic Chemistry - X-MOL
Cycloheptyl substituted N-heterocyclic carbene PEPPSI-type palladium complexes with different N-coordinated ligands: Involvement in Suzuki-Miyaura reaction - J. Organomet. Chem. - X-MOL
The palladium-imidazole complexes I-V used in these studies. | Download Scientific Diagram
The palladium-imidazole complexes I-V used in these studies. | Download Scientific Diagram
1H-Imidazole - palladium (1:1) | C3H4N2Pd | ChemSpider
Palladium–imidazole derivatives as highly active catalysts for Heck reactions - ScienceDirect
Structure, dynamics and catalytic activity of palladium(II) complexes with imidazole ligands - ScienceDirect
Mechanistic Studies on the Palladium‐Catalyzed Direct C‐5 Arylation of Imidazoles: The Fundamental Role of the Azole as a Ligand for Palladium - Perego - 2016 - Advanced Synthesis & Catalysis - Wiley Online Library
Dimetallic Palladium‐NHC Complexes: Synthesis, Characterization, and Catalytic Application for Direct C−H Arylation Reaction of Heteroaromatics with Aryl Chlorides - Adv. Synth. Catal. - X-MOL
The palladium-imidazole complexes I-V used in these studies. | Download Scientific Diagram
![PDF) Mixed Ligand, Palladium(II) and Platinum(II) Complexes of Tertiary Diphosphines with S-1H Benzo[D] Imidazole-2-Yl Benzothioate](https://i1.rgstatic.net/publication/316589515_Mixed_Ligand_PalladiumII_and_PlatinumII_Complexes_of_Tertiary_Diphosphines_with_S-1H_BenzoD_Imidazole-2-Yl_Benzothioate/links/5a1e819faca272cbfbc04f0f/largepreview.png "PDF) Mixed Ligand, Palladium(II) and Platinum(II) Complexes of Tertiary Diphosphines with S-1H Benzo[D] Imidazole-2-Yl Benzothioate")
PDF) Mixed Ligand, Palladium(II) and Platinum(II) Complexes of Tertiary Diphosphines with S-1H Benzo[D] Imidazole-2-Yl Benzothioate
The palladium-imidazole complexes I-V used in these studies. | Download Scientific Diagram
Palladium-catalyzed tandem one-pot synthesis of π-expanded imidazoles through a sequential Heck and oxidative amination reaction - Organic & Biomolecular Chemistry (RSC Publishing)
Completely N1-selective palladium-catalyzed arylation of unsymmetric imidazoles: application to the synthesis of nilotinib. - Abstract - Europe PMC
Recent Progress in the Use of Pd-Catalyzed C-C Cross-Coupling Reactions in the Synthesis of Pharmaceutical Compounds
The First Example of Palladium(II)-Catalyzed Oxidative C–N Cross Coupling of 2 H -Imidazole 1-Oxide with Azoles | SpringerLink
![884879-23-6 | PHENYLALLYLCHLORO-[1,3-BIS(DIISOPROPYLPHENYL)IMIDAZOLE -2-YLIDENE]PALLADIUM(II) | Hangzhou Keying Chem Co., Ltd.](https://qncdn.chemcd.cn/keying/structure/KY155655.png "884879-23-6 | PHENYLALLYLCHLORO-[1,3-BIS(DIISOPROPYLPHENYL)IMIDAZOLE -2-YLIDENE]PALLADIUM(II) | Hangzhou Keying Chem Co., Ltd.")
884879-23-6 | PHENYLALLYLCHLORO-[1,3-BIS(DIISOPROPYLPHENYL)IMIDAZOLE -2-YLIDENE]PALLADIUM(II) | Hangzhou Keying Chem Co., Ltd.
![PalladiuM, [1,3-bis[2,6-bis(1-Methylethyl)phenyl]-1,3-dihydro-2H-iMidazol-2-ylidene]dichloro(1-Methyl-1H- iMidazole-kN3)-, (SP-4-1)- | 1314876-23-7](https://www.chemicalbook.com/CAS/20180906/GIF/1314876-23-7.gif "PalladiuM, [1,3-bis[2,6-bis(1-Methylethyl)phenyl]-1,3-dihydro-2H-iMidazol-2-ylidene]dichloro(1-Methyl-1H- iMidazole-kN3)-, (SP-4-1)- | 1314876-23-7")
PalladiuM, [1,3-bis[2,6-bis(1-Methylethyl)phenyl]-1,3-dihydro-2H-iMidazol-2-ylidene]dichloro(1-Methyl-1H- iMidazole-kN3)-, (SP-4-1)- | 1314876-23-7
