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mírné odhalit vaření palladium imidazole minulost Okoun sýr

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

Palladium-catalyzed tandem one-pot synthesis of π-expanded imidazoles  through a sequential Heck and oxidative amination reaction - Organic &  Biomolecular Chemistry (RSC Publishing)
Palladium-catalyzed tandem one-pot synthesis of π-expanded imidazoles through a sequential Heck and oxidative amination reaction - Organic & Biomolecular Chemistry (RSC Publishing)

Recent Progress in the Use of Pd-Catalyzed C-C Cross-Coupling Reactions in  the Synthesis of Pharmaceutical Compounds
Recent Progress in the Use of Pd-Catalyzed C-C Cross-Coupling Reactions in the Synthesis of Pharmaceutical Compounds

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
The palladium-imidazole complexes I-V used in these studies. | Download Scientific Diagram

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.

Novel palladium imidazole catalysts for Suzuki cross-coupling reactions.
Novel palladium imidazole catalysts for Suzuki cross-coupling reactions.

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

1H-Imidazole - palladium (1:1) | C3H4N2Pd | ChemSpider
1H-Imidazole - palladium (1:1) | C3H4N2Pd | ChemSpider

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

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

Polymer-supported palladium-imidazole complex catalyst for hydrogenation of  substituted benzylideneanilines - ScienceDirect
Polymer-supported palladium-imidazole complex catalyst for hydrogenation of substituted benzylideneanilines - ScienceDirect

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

Polymer-supported palladium-imidazole complex catalyst for hydrogenation of  substituted benzylideneanilines - ScienceDirect
Polymer-supported palladium-imidazole complex catalyst for hydrogenation of substituted benzylideneanilines - ScienceDirect

Air-stable imidazole-imine palladium complexes for Suzuki–Miyaura coupling:  Toward an efficient, green synthesis of biaryl compounds - ScienceDirect
Air-stable imidazole-imine palladium complexes for Suzuki–Miyaura coupling: Toward an efficient, green synthesis of biaryl compounds - ScienceDirect

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.

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

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

The First Example of Palladium(II)-Catalyzed Oxidative C–N Cross Coupling  of 2 H -Imidazole 1-Oxide with Azoles | SpringerLink
The First Example of Palladium(II)-Catalyzed Oxidative C–N Cross Coupling of 2 H -Imidazole 1-Oxide with Azoles | SpringerLink

Air-stable imidazole-imine palladium complexes for Suzuki–Miyaura coupling:  Toward an efficient, green synthesis of biaryl compounds - ScienceDirect
Air-stable imidazole-imine palladium complexes for Suzuki–Miyaura coupling: Toward an efficient, green synthesis of biaryl compounds - ScienceDirect

Cycloheptyl substituted N-heterocyclic carbene PEPPSI-type palladium  complexes with different N-coordinated ligands: Involvement in  Suzuki-Miyaura reaction - J. Organomet. Chem. - 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

A thiosemicarbazone–palladium(II)–imidazole complex as an efficient  pre-catalyst for Suzuki–Miyaura cross-coupling reactions at room  temperature in aqueous media | SpringerLink
A thiosemicarbazone–palladium(II)–imidazole complex as an efficient pre-catalyst for Suzuki–Miyaura cross-coupling reactions at room temperature in aqueous media | SpringerLink

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

Palladium–imidazole derivatives as highly active catalysts for Heck  reactions - ScienceDirect
Palladium–imidazole derivatives as highly active catalysts for Heck reactions - ScienceDirect

Palladium| BLD Pharm
Palladium| BLD Pharm

Palladium(2+) (3-ethenidyl-1,1,3,3-tetramethyldisiloxanyl)ethenide -  1,3-dimesityl-2,3-dihydro-1H-imidazole (1:1:1) | C29H42N2OPdSi2 | ChemSpider
Palladium(2+) (3-ethenidyl-1,1,3,3-tetramethyldisiloxanyl)ethenide - 1,3-dimesityl-2,3-dihydro-1H-imidazole (1:1:1) | C29H42N2OPdSi2 | ChemSpider

Synthesis, crystal structures, and catalytic activities of palladium  imidazole complexes formed by 2-hydroxyethyl group cleavage | SpringerLink
Synthesis, crystal structures, and catalytic activities of palladium imidazole complexes formed by 2-hydroxyethyl group cleavage | SpringerLink