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Keňa Speciální pluk palladium catalysis tetramethylethylenediamine Existuje trend Úzce Spíše

Aerobic Copper Catalytic Oxidation of Methylene and Arylidenebisnaphthols:  A Green and Efficient Synthesis of Spironaphthalenones - ChemistrySelect -  X-MOL
Aerobic Copper Catalytic Oxidation of Methylene and Arylidenebisnaphthols: A Green and Efficient Synthesis of Spironaphthalenones - ChemistrySelect - X-MOL

Regioselective and Stereospecific Cross‐Coupling of Primary Allylic Amines  with Boronic Acids and Boronates through Palladium‐Catalyzed CN Bond  Cleavage - Li - 2012 - Angewandte Chemie International Edition - Wiley  Online Library
Regioselective and Stereospecific Cross‐Coupling of Primary Allylic Amines with Boronic Acids and Boronates through Palladium‐Catalyzed CN Bond Cleavage - Li - 2012 - Angewandte Chemie International Edition - Wiley Online Library

Catalytic activity of Pd and Cu in the studied cross-coupling reaction |  Download Table
Catalytic activity of Pd and Cu in the studied cross-coupling reaction | Download Table

NaBH4-TMEDA and a palladium catalyst as efficient regio- and chemoselective  system for the hydrodehalogenation of halogenated heterocycles -  ScienceDirect
NaBH4-TMEDA and a palladium catalyst as efficient regio- and chemoselective system for the hydrodehalogenation of halogenated heterocycles - ScienceDirect

Pd-Catalyzed Cross-Coupling Reactions | Sigma-Aldrich
Pd-Catalyzed Cross-Coupling Reactions | Sigma-Aldrich

Catalysts | Free Full-Text | Microwave-Assisted Palladium-Catalyzed  Cross-Coupling Reactions: Generation of Carbon–Carbon Bond | HTML
Catalysts | Free Full-Text | Microwave-Assisted Palladium-Catalyzed Cross-Coupling Reactions: Generation of Carbon–Carbon Bond | HTML

N,N,N′,N′‐Tetramethylethylenediamine - Haynes - - Major Reference Works -  Wiley Online Library
N,N,N′,N′‐Tetramethylethylenediamine - Haynes - - Major Reference Works - Wiley Online Library

One-pot synthesis of self-assembled heteroleptic palladium(II) complexes  with tmeda: An application of ligand exchange reactions - ScienceDirect
One-pot synthesis of self-assembled heteroleptic palladium(II) complexes with tmeda: An application of ligand exchange reactions - ScienceDirect

EP2107047A1 - Method for producing organic compounds by means of a  transition metal-catalysed cross-coupling reaction of an aryl-X,  heteroaryl-X, cycloalkenyl-X or alkenyl-X compound with an alkyl, alkenyl,  cycloalkyl or cycloalkenyl halogenide -
EP2107047A1 - Method for producing organic compounds by means of a transition metal-catalysed cross-coupling reaction of an aryl-X, heteroaryl-X, cycloalkenyl-X or alkenyl-X compound with an alkyl, alkenyl, cycloalkyl or cycloalkenyl halogenide -

Mixed-Ligand Approach to Palladium-Catalyzed Direct Arylation  Polymerization: Effective Prevention of Structural Defects Using Diamines -  Macromolecules - X-MOL
Mixed-Ligand Approach to Palladium-Catalyzed Direct Arylation Polymerization: Effective Prevention of Structural Defects Using Diamines - Macromolecules - X-MOL

Catalysts | Free Full-Text | Microwave-Assisted Palladium-Catalyzed  Cross-Coupling Reactions: Generation of Carbon–Carbon Bond | HTML
Catalysts | Free Full-Text | Microwave-Assisted Palladium-Catalyzed Cross-Coupling Reactions: Generation of Carbon–Carbon Bond | HTML

Palladium-catalyzed decarboxylative gem-selective addition of alkynoic  acids to terminal alkynes - Organic Chemistry Frontiers (RSC Publishing)
Palladium-catalyzed decarboxylative gem-selective addition of alkynoic acids to terminal alkynes - Organic Chemistry Frontiers (RSC Publishing)

Figure 1 from Palladium-catalyzed enantioselective alpha-arylation and  alpha-vinylation of oxindoles facilitated by an axially chiral  P-stereogenic ligand. | Semantic Scholar
Figure 1 from Palladium-catalyzed enantioselective alpha-arylation and alpha-vinylation of oxindoles facilitated by an axially chiral P-stereogenic ligand. | Semantic Scholar

PDF) Complexes of Palladium with Tetramethylethylenediamine and their  Properties
PDF) Complexes of Palladium with Tetramethylethylenediamine and their Properties

Designed heterogeneous palladium catalysts for reversible light-controlled  bioorthogonal catalysis in living cells | Nature Communications
Designed heterogeneous palladium catalysts for reversible light-controlled bioorthogonal catalysis in living cells | Nature Communications

Catalysts | Free Full-Text | Microwave-Assisted Palladium-Catalyzed  Cross-Coupling Reactions: Generation of Carbon–Carbon Bond | HTML
Catalysts | Free Full-Text | Microwave-Assisted Palladium-Catalyzed Cross-Coupling Reactions: Generation of Carbon–Carbon Bond | HTML

Dichloro(N,N,N′,N′-tetramethylethylenediamine)palladium(II) 99 % |  14267-08-4 | Sigma-Aldrich
Dichloro(N,N,N′,N′-tetramethylethylenediamine)palladium(II) 99 % | 14267-08-4 | Sigma-Aldrich

Mixed-Ligand Approach to Palladium-Catalyzed Direct Arylation  Polymerization: Synthesis of Donor–Acceptor Polymers Containing  Unsubstituted Bithiophene Units - Macromolecules - X-MOL
Mixed-Ligand Approach to Palladium-Catalyzed Direct Arylation Polymerization: Synthesis of Donor–Acceptor Polymers Containing Unsubstituted Bithiophene Units - Macromolecules - X-MOL

Catalysts | Free Full-Text | Microwave-Assisted Palladium-Catalyzed  Cross-Coupling Reactions: Generation of Carbon–Carbon Bond | HTML
Catalysts | Free Full-Text | Microwave-Assisted Palladium-Catalyzed Cross-Coupling Reactions: Generation of Carbon–Carbon Bond | HTML

Palladium(II)-catalyzed C-H activation/C-C cross-coupling reactions:  versatility and practicality. - Abstract - Europe PMC
Palladium(II)-catalyzed C-H activation/C-C cross-coupling reactions: versatility and practicality. - Abstract - Europe PMC

Greening Up” Cross-Coupling Chemistry | SpringerLink
Greening Up” Cross-Coupling Chemistry | SpringerLink

EP2107047A1 - Method for producing organic compounds by means of a  transition metal-catalysed cross-coupling reaction of an aryl-X,  heteroaryl-X, cycloalkenyl-X or alkenyl-X compound with an alkyl, alkenyl,  cycloalkyl or cycloalkenyl halogenide -
EP2107047A1 - Method for producing organic compounds by means of a transition metal-catalysed cross-coupling reaction of an aryl-X, heteroaryl-X, cycloalkenyl-X or alkenyl-X compound with an alkyl, alkenyl, cycloalkyl or cycloalkenyl halogenide -

Hydrodehalogenation of halogenated pyridines and quinolines by sodium  borohydride/N,N,N′,N′-tetramethylethylenediamine under palladium catalysis
Hydrodehalogenation of halogenated pyridines and quinolines by sodium borohydride/N,N,N′,N′-tetramethylethylenediamine under palladium catalysis

Hydrodehalogenation of halogenated pyridines and quinolines by sodium  borohydride/N,N,N′,N′-tetramethylethylenediamine under palladium catalysis  - ScienceDirect
Hydrodehalogenation of halogenated pyridines and quinolines by sodium borohydride/N,N,N′,N′-tetramethylethylenediamine under palladium catalysis - ScienceDirect