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Hertsoginna Kulutused desinfitseerima phosphorus oxygen ligand for palladium Frank Worthley Suunamine Vastuseks

Phosphorus - Nitrogen ligands. | Download Scientific Diagram
Phosphorus - Nitrogen ligands. | Download Scientific Diagram

Metal-Ligand Cooperativity of Phosphorus-Containing Pincer Systems |  SpringerLink
Metal-Ligand Cooperativity of Phosphorus-Containing Pincer Systems | SpringerLink

Agarose functionalized phosphorus ligand for stabilization of small-sized  palladium and copper nanoparticles: efficient heterogeneous catalyst for  Sonogashira reaction - ScienceDirect
Agarose functionalized phosphorus ligand for stabilization of small-sized palladium and copper nanoparticles: efficient heterogeneous catalyst for Sonogashira reaction - ScienceDirect

New palladium (II) complexes containing phosphine‐nitrogen ligands and  their use as catalysts in aminocarbonylation reaction - Aranda - 2019 -  Applied Organometallic Chemistry - Wiley Online Library
New palladium (II) complexes containing phosphine‐nitrogen ligands and their use as catalysts in aminocarbonylation reaction - Aranda - 2019 - Applied Organometallic Chemistry - Wiley Online Library

Dialkylbiaryl phosphine ligands - Wikipedia
Dialkylbiaryl phosphine ligands - Wikipedia

Chiral Bifunctional Phosphine‐Carboxylate Ligands for Palladium(0)‐Catalyzed  Enantioselective C−H Arylation - Yang - 2018 - Angewandte Chemie  International Edition - Wiley Online Library
Chiral Bifunctional Phosphine‐Carboxylate Ligands for Palladium(0)‐Catalyzed Enantioselective C−H Arylation - Yang - 2018 - Angewandte Chemie International Edition - Wiley Online Library

Hybrid cycloolefin ligands for palladium–olefin cooperative catalysis |  Nature Synthesis
Hybrid cycloolefin ligands for palladium–olefin cooperative catalysis | Nature Synthesis

Parameterization of phosphine ligands demonstrates enhancement of nickel  catalysis via remote steric effects | Nature Chemistry
Parameterization of phosphine ligands demonstrates enhancement of nickel catalysis via remote steric effects | Nature Chemistry

Synthesis, characterization, coordination chemistry, and luminescence  studies of copper, silver, palladium, and platinum complexes with a  phosphorus/nitrogen/phosphorus ligand - ScienceDirect
Synthesis, characterization, coordination chemistry, and luminescence studies of copper, silver, palladium, and platinum complexes with a phosphorus/nitrogen/phosphorus ligand - ScienceDirect

Synthesis of 3-aryl-2-phosphinoimidazo[1,2- a ]pyridine ligands for use in  palladium-catalyzed cross-coupling reactions - RSC Advances (RSC  Publishing) DOI:10.1039/C9RA02200G
Synthesis of 3-aryl-2-phosphinoimidazo[1,2- a ]pyridine ligands for use in palladium-catalyzed cross-coupling reactions - RSC Advances (RSC Publishing) DOI:10.1039/C9RA02200G

Phosphorus-based ligand facilitates palladium-catalyzed complex molecules
Phosphorus-based ligand facilitates palladium-catalyzed complex molecules

Tang Group-Research Publications
Tang Group-Research Publications

DPPBA ligands in palladium-catalyzed AAA reactions. | Download Scientific  Diagram
DPPBA ligands in palladium-catalyzed AAA reactions. | Download Scientific Diagram

Hybrid cycloolefin ligands for palladium–olefin cooperative catalysis |  Nature Synthesis
Hybrid cycloolefin ligands for palladium–olefin cooperative catalysis | Nature Synthesis

Phosphorus - Nitrogen ligands. | Download Scientific Diagram
Phosphorus - Nitrogen ligands. | Download Scientific Diagram

Pd(OAc)2-catalyzed asymmetric hydrogenation of sterically hindered  N-tosylimines | Nature Communications
Pd(OAc)2-catalyzed asymmetric hydrogenation of sterically hindered N-tosylimines | Nature Communications

Palladium-catalyzed phosphorus–carbon bond formation: cross-coupling  reactions of alkyl phosphinates with aryl, heteroaryl, alkenyl, benzylic,  and allylic halides and triflates - ScienceDirect
Palladium-catalyzed phosphorus–carbon bond formation: cross-coupling reactions of alkyl phosphinates with aryl, heteroaryl, alkenyl, benzylic, and allylic halides and triflates - ScienceDirect

Catalysts | Free Full-Text | Preparation and Catalytic Performance of  Metal-Rich Pd Phosphides for the Solvent-Free Selective Hydrogenation of  Chloronitrobenzene | HTML
Catalysts | Free Full-Text | Preparation and Catalytic Performance of Metal-Rich Pd Phosphides for the Solvent-Free Selective Hydrogenation of Chloronitrobenzene | HTML

Ligand-centered reactivity of a pseudo-dearomatized phosphorus-nitrogen PN  3 P* rhodium complex towards molecular oxygen at room temperature -  Inorganic Chemistry Frontiers (RSC Publishing) DOI:10.1039/C9QI01605H
Ligand-centered reactivity of a pseudo-dearomatized phosphorus-nitrogen PN 3 P* rhodium complex towards molecular oxygen at room temperature - Inorganic Chemistry Frontiers (RSC Publishing) DOI:10.1039/C9QI01605H

研究成果 | 大阪大学大学院基礎工学研究科 新谷研究室
研究成果 | 大阪大学大学院基礎工学研究科 新谷研究室

Ligand-centered reactivity of a pseudo-dearomatized phosphorus-nitrogen PN  3 P* rhodium complex towards molecular oxygen at room temperature -  Inorganic Chemistry Frontiers (RSC Publishing) DOI:10.1039/C9QI01605H
Ligand-centered reactivity of a pseudo-dearomatized phosphorus-nitrogen PN 3 P* rhodium complex towards molecular oxygen at room temperature - Inorganic Chemistry Frontiers (RSC Publishing) DOI:10.1039/C9QI01605H

Cationic palladium(II)–acetylacetonate complexes containing phosphine and  aminophosphine ligands and their catalytic activities in telomerization of  1,3-butadiene with methanol - ScienceDirect
Cationic palladium(II)–acetylacetonate complexes containing phosphine and aminophosphine ligands and their catalytic activities in telomerization of 1,3-butadiene with methanol - ScienceDirect

Ligand-centered reactivity of a pseudo-dearomatized phosphorus-nitrogen PN  3 P* rhodium complex towards molecular oxygen at room temperature -  Inorganic Chemistry Frontiers (RSC Publishing) DOI:10.1039/C9QI01605H
Ligand-centered reactivity of a pseudo-dearomatized phosphorus-nitrogen PN 3 P* rhodium complex towards molecular oxygen at room temperature - Inorganic Chemistry Frontiers (RSC Publishing) DOI:10.1039/C9QI01605H