![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](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
![Structure, dynamics and catalytic activity of palladium(II) complexes with imidazole ligands - ScienceDirect Structure, dynamics and catalytic activity of palladium(II) complexes with imidazole ligands - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0020169310005785-gr7.jpg)
Structure, dynamics and catalytic activity of palladium(II) complexes with imidazole ligands - ScienceDirect
![Completely N1-selective palladium-catalyzed arylation of unsymmetric imidazoles: application to the synthesis of nilotinib. - Abstract - Europe PMC Completely N1-selective palladium-catalyzed arylation of unsymmetric imidazoles: application to the synthesis of nilotinib. - Abstract - Europe PMC](https://europepmc.org/articles/PMC3257364/bin/nihms341879f1.jpg)
Completely N1-selective palladium-catalyzed arylation of unsymmetric imidazoles: application to the synthesis of nilotinib. - Abstract - Europe PMC
![C-H bonds as ubiquitous functionality: a general approach to complex arylated imidazoles via regioselective sequential arylation of all three C-H bonds and regioselective N-alkylation enabled by SEM-group transposition. - Abstract - Europe C-H bonds as ubiquitous functionality: a general approach to complex arylated imidazoles via regioselective sequential arylation of all three C-H bonds and regioselective N-alkylation enabled by SEM-group transposition. - Abstract - Europe](https://europepmc.org/articles/PMC2971672/bin/nihms245438f8.jpg)
C-H bonds as ubiquitous functionality: a general approach to complex arylated imidazoles via regioselective sequential arylation of all three C-H bonds and regioselective N-alkylation enabled by SEM-group transposition. - Abstract - Europe
New asymmetric synthesis of protein farnesyltransferase inhibitors via palladium-catalyzed cross-coupling reactions of 2-iodo-imidazoles - Organic & Biomolecular Chemistry (RSC Publishing)
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Polymer-supported palladium-imidazole complex catalyst for hydrogenation of substituted benzylideneanilines - ScienceDirect
![A palladium-catalyzed synthesis of (hetero)aryl-substituted imidazoles from aryl halides, imines and carbon monoxide - Chemical Science (RSC Publishing) A palladium-catalyzed synthesis of (hetero)aryl-substituted imidazoles from aryl halides, imines and carbon monoxide - Chemical Science (RSC Publishing)](https://pubs.rsc.org/image/article/2017/sc/c6sc04371b/c6sc04371b-f1_hi-res.gif)
A palladium-catalyzed synthesis of (hetero)aryl-substituted imidazoles from aryl halides, imines and carbon monoxide - Chemical Science (RSC Publishing)
![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 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](https://onlinelibrary.wiley.com/cms/asset/9d6eca4a-d110-4ea8-bc82-f8693d13cf42/mcontent.jpg)
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 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](https://xpic.x-mol.com/20191218%2F10.1002_adsc.201901189.jpg)
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
![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](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
![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.](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.
![Figure 2 from Self-assembled poly(imidazole-palladium): highly active, reusable catalyst at parts per million to parts per billion levels. | Semantic Scholar Figure 2 from Self-assembled poly(imidazole-palladium): highly active, reusable catalyst at parts per million to parts per billion levels. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/58903b1e784111e4dc9aedfc4f31b8b7d5c00034/3-Figure2-1.png)
Figure 2 from Self-assembled poly(imidazole-palladium): highly active, reusable catalyst at parts per million to parts per billion levels. | Semantic Scholar
![Table 2 from SYNTHESIS AND STRUCTURE OF TWO PALLADIUM(II) COMPLEXES BEARING ACETONITRILE AND N-HETEROCYCLIC CARBENE DERIVED FROM IMIDAZOLE | Semantic Scholar Table 2 from SYNTHESIS AND STRUCTURE OF TWO PALLADIUM(II) COMPLEXES BEARING ACETONITRILE AND N-HETEROCYCLIC CARBENE DERIVED FROM IMIDAZOLE | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/103365ea6f8be72be107f0a9302e035cd032b79a/4-Table2-1.png)
Table 2 from SYNTHESIS AND STRUCTURE OF TWO PALLADIUM(II) COMPLEXES BEARING ACETONITRILE AND N-HETEROCYCLIC CARBENE DERIVED FROM IMIDAZOLE | Semantic Scholar
![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.](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.
![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](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
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Tetranuclear Palladium Complexes of Abnormal N‐Heterocyclic Carbene Ligands and their Catalytic Activities in Mizoroki‐Heck Coupling Reaction of Electron‐Rich Aryl Chlorides - Lee - 2019 - Advanced Synthesis & Catalysis - Wiley Online Library
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