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koryto kouř legislativa palladium triflate právník návrhář dusík

Palladium‐Catalyzed Fluorination of Cyclic Vinyl Triflates: Effect of  TESCF3 as an Additive - Angew. Chem. Int. Ed. - X-MOL
Palladium‐Catalyzed Fluorination of Cyclic Vinyl Triflates: Effect of TESCF3 as an Additive - Angew. Chem. Int. Ed. - X-MOL

Triflates - an overview | ScienceDirect Topics
Triflates - an overview | ScienceDirect Topics

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

Palladium‐Catalyzed Trifluoroethylation of Benzo[h]quinoline Derivatives by  Mesityl(2,2,2‐trifluoroethyl)iodonium Triflate - Asian J. Org. Chem. - X-MOL
Palladium‐Catalyzed Trifluoroethylation of Benzo[h]quinoline Derivatives by Mesityl(2,2,2‐trifluoroethyl)iodonium Triflate - Asian J. Org. Chem. - X-MOL

Org. Synth. 2011, 88, 260
Org. Synth. 2011, 88, 260

Examination of palladium-catalyzed vinylation of enol phosphate 28... |  Download Table
Examination of palladium-catalyzed vinylation of enol phosphate 28... | Download Table

Synthesis of N-Arylpyrazoles by Palladium-Catalyzed Coupling of Aryl  Triflates with Pyrazole Derivatives - J. Org. Chem. - X-MOL
Synthesis of N-Arylpyrazoles by Palladium-Catalyzed Coupling of Aryl Triflates with Pyrazole Derivatives - J. Org. Chem. - X-MOL

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

An Improved Palladium-Catalyzed Conversion of Aryl and Vinyl Triflates to  Bromides and Chlorides
An Improved Palladium-Catalyzed Conversion of Aryl and Vinyl Triflates to Bromides and Chlorides

1,3-Bis(diphenylphosphino)propane]palladium(II) triflate | 137846-38-9 |  Sigma-Aldrich
1,3-Bis(diphenylphosphino)propane]palladium(II) triflate | 137846-38-9 | Sigma-Aldrich

Halide-free highly-pure imidazolium triflate ionic liquids: Preparation and  use in palladium-catalysed allylic alkylation - Green Chemistry (RSC  Publishing)
Halide-free highly-pure imidazolium triflate ionic liquids: Preparation and use in palladium-catalysed allylic alkylation - Green Chemistry (RSC Publishing)

Palladium(II) trifluoroacetate 97 % | 42196-31-6 | Sigma-Aldrich
Palladium(II) trifluoroacetate 97 % | 42196-31-6 | Sigma-Aldrich

Palladium triflate | C2F6O6PdS2 - PubChem
Palladium triflate | C2F6O6PdS2 - PubChem

R)-(+)-2,2′-Bis(diphenylphosphino)-1,1′-binaphthyl]-diaquo-palladium(II)  bis(triflate) | Sigma-Aldrich
R)-(+)-2,2′-Bis(diphenylphosphino)-1,1′-binaphthyl]-diaquo-palladium(II) bis(triflate) | Sigma-Aldrich

Metal catalyzed defunctionalization reactions - Organic & Biomolecular  Chemistry (RSC Publishing) DOI:10.1039/C5OB01949D
Metal catalyzed defunctionalization reactions - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C5OB01949D

Palladium-catalyzed triethylammonium formate reduction of aryl triflates. A  selective method for the deoxygenation of phenols - ScienceDirect
Palladium-catalyzed triethylammonium formate reduction of aryl triflates. A selective method for the deoxygenation of phenols - ScienceDirect

Palladium-catalyzed phosphination of functionalized aryl triflates -  ScienceDirect
Palladium-catalyzed phosphination of functionalized aryl triflates - ScienceDirect

SYNTHESIS OF CEPHALOSPORIN COMPOUNDS - US 2019 263,831 A1 - PatentSwarm
SYNTHESIS OF CEPHALOSPORIN COMPOUNDS - US 2019 263,831 A1 - PatentSwarm

Nucleophilic palladium-catalysed Ar−F bond-forming reaction. a, The... |  Download Scientific Diagram
Nucleophilic palladium-catalysed Ar−F bond-forming reaction. a, The... | Download Scientific Diagram

Palladium(2+) bis(trifluoromethanesulfonate) | C2F6O6PdS2 | ChemSpider
Palladium(2+) bis(trifluoromethanesulfonate) | C2F6O6PdS2 | ChemSpider

R)-(+)-2,2′-Bis(diphenylphosphino)-1,1′-binaphthyl]-diaquo-palladium(II)  bis(triflate) | Sigma-Aldrich
R)-(+)-2,2′-Bis(diphenylphosphino)-1,1′-binaphthyl]-diaquo-palladium(II) bis(triflate) | Sigma-Aldrich

Scheme 1. General reaction for the Suzuki-Miyaura palladium-catalyzed... |  Download Scientific Diagram
Scheme 1. General reaction for the Suzuki-Miyaura palladium-catalyzed... | Download Scientific Diagram

Aryl bromide/triflate selectivities reveal mechanistic divergence in  palladium-catalysed couplings; the Suzuki–Miyaura anomaly - Chemical  Communications (RSC Publishing) DOI:10.1039/B701517H
Aryl bromide/triflate selectivities reveal mechanistic divergence in palladium-catalysed couplings; the Suzuki–Miyaura anomaly - Chemical Communications (RSC Publishing) DOI:10.1039/B701517H