| P50 | author | Franziska Schoenebeck | Q21259890 |
| | Indrek Kalvet | Q41192889 |
| | Ignacio Funes-Ardoiz | Q57543580 |
| P2093 | author name string | Guillaume Magnin | |
| | Kristina Deckers | |
| | Theresa Sperger | |
| | Marius Kremer | |
| P2860 | cites work | Overcoming lability of extremely long alkane carbon–carbon bonds through dispersion forces | Q57742709 |
| | Modular Functionalization of Arenes in a Triply Selective Sequence: Rapid C(sp ) and C(sp ) Coupling of C-Br, C-OTf, and C-Cl Bonds Enabled by a Single Palladium(I) Dimer | Q58700041 |
| | Computational Studies of Synthetically Relevant Homogeneous Organometallic Catalysis Involving Ni, Pd, Ir, and Rh: An Overview of Commonly Employed DFT Methods and Mechanistic Insights | Q60240345 |
| | On the Accuracy of DFT Methods in Reproducing Ligand Substitution Energies for Transition Metal Complexes in Solution: The Role of Dispersive Interactions | Q64028157 |
| | Studies of Palladium-Catalyzed Cross-Coupling Reactions for Preparation of Highly Hindered Biaryls Relevant to the Korupensamine/Michellamine Problem | Q74824711 |
| | Aryl bromide/triflate selectivities reveal mechanistic divergence in palladium-catalysed couplings; the Suzuki-Miyaura anomaly | Q80212663 |
| | Nickel-catalyzed cross-coupling reaction of aryl fluorides and chlorides with grignard reagents under nickel/magnesium bimetallic cooperation | Q82032153 |
| | Experimental and theoretical investigations of new dinuclear palladium complexes as precatalysts for the amination of aryl chlorides | Q83307782 |
| | Efficient synthesis of sterically hindered arenes bearing acyclic secondary alkyl groups by Suzuki-Miyaura cross-couplings | Q86617725 |
| | Making natural products from renewable feedstocks: back to the roots? | Q90789160 |
| | Arylation of Axially Chiral Phosphorothioate Salts by Dinuclear PdI Catalysis | Q92694341 |
| | Generation and Cross-Coupling of Organozinc Reagents in Flow | Q93067386 |
| | Corrigendum: Palladium(I) Dimer Enabled Extremely Rapid and Chemoselective Alkylation of Aryl Bromides over Triflates and Chlorides in Air | Q94507951 |
| | Corrigendum: Rapid Room-Temperature, Chemoselective C sp2 -C sp2 Coupling of Poly(pseudo)halogenated Arenes Enabled by Palladium(I) Catalysis in Air | Q94507955 |
| | Negishi coupling of secondary alkylzinc halides with aryl bromides and chlorides | Q24651734 |
| | Aryl-aryl bond formation one century after the discovery of the Ullmann reaction | Q28216892 |
| | Steric Crowding Can Stabilize a Labile Molecule: Solving the Hexaphenylethane Riddle | Q29306239 |
| | Reactivity and stability of dinuclear Pd(I) complexes: studies on the active catalytic species, insights into precatalyst activation and deactivation, and application in highly selective cross-coupling reactions | Q34088338 |
| | The lipophilic bullet hits the targets: medicinal chemistry of adamantane derivatives | Q34329204 |
| | The mechanisms of the Stille reaction | Q34348133 |
| | Adamantyl cannabinoids: a novel class of cannabinergic ligands | Q34431603 |
| | Palladium-catalyzed coupling reactions of aryl chlorides | Q34998714 |
| | Regioselective (site-selective) functionalization of unsaturated halogenated nitrogen, oxygen and sulfur heterocycles by Pd-catalysed cross-couplings and direct arylation processes | Q36852261 |
| | Redox-Active Esters in Fe-Catalyzed C-C Coupling | Q37243448 |
| | Recent advances in aryl-aryl bond formation by direct arylation. | Q37558306 |
| | London dispersion in molecular chemistry--reconsidering steric effects. | Q38564398 |
| | Site-selective Suzuki-Miyaura coupling of heteroaryl halides - understanding the trends for pharmaceutically important classes. | Q38815720 |
| | Parameterization of phosphine ligands reveals mechanistic pathways and predicts reaction outcomes | Q38863042 |
| | The discovery of potent nonstructural protein 5A (NS5A) inhibitors with a unique resistance profile-Part 1. | Q39004462 |
| | Highly Efficient C-SeCF3 Coupling of Aryl Iodides Enabled by an Air-Stable Dinuclear Pd(I) Catalyst | Q40789740 |
| | Trifluoromethylthiolation of aryl iodides and bromides enabled by a bench-stable and easy-to-recover dinuclear palladium(i) catalyst | Q41012429 |
| | Palladium(I) Dimer Enabled Extremely Rapid and Chemoselective Alkylation of Aryl Bromides over Triflates and Chlorides in Air. | Q41019125 |
| | Rapid Room-Temperature, Chemoselective Csp2 -Csp2 Coupling of Poly(pseudo)halogenated Arenes Enabled by Palladium(I) Catalysis in Air. | Q41841800 |
| | Ligand-controlled regioselectivity in palladium-catalyzed cross coupling reactions | Q43178644 |
| | Solvent effect on palladium-catalyzed cross-coupling reactions and implications on the active catalytic species | Q44438586 |
| | Origin of regioselectivity in palladium-catalyzed cross-coupling reactions of polyhalogenated heterocycles | Q46175568 |
| | Accurate modelling of Pd(0) + PhX oxidative addition kinetics | Q46617713 |
| | Computed ligand effects on the oxidative addition of phenyl halides to phosphine supported palladium(0) catalysts | Q46856632 |
| | Efficient synthesis of sterically crowded biaryls by palladium-phosphinous acid-catalyzed cross-coupling of aryl halides and aryl grignards | Q46871744 |
| | Visible-Light-Driven Palladium-Catalyzed Radical Alkylation of C-H Bonds with Unactivated Alkyl Bromides. | Q47430115 |
| | Enabling the Cross-Coupling of Tertiary Organoboron Nucleophiles through Radical-Mediated Alkyl Transfer | Q48107967 |
| | Ligand-Substrate Dispersion Facilitates the Copper-Catalyzed Hydroamination of Unactivated Olefins. | Q48136882 |
| | Mechanically induced chemiluminescence from polymers incorporating a 1,2-dioxetane unit in the main chain | Q50245216 |
| | A general palladium-catalyzed method for alkylation of heteroarenes using secondary and tertiary alkyl halides. | Q51028481 |
| | A new class of synthetic retinoid antibiotics effective against bacterial persisters. | Q52690308 |
| | Unexpected Rearrangement of 2-Bromoaniline under Biphasic Alkylation Conditions. | Q55222612 |
| | Monochromatic Electron Photoemission from Diamondoid Monolayers | Q56136933 |
| | Unparalleled Rates for the Activation of Aryl Chlorides and Bromides: Coupling with Amines and Boronic Acids in Minutes at Room Temperature | Q56688216 |
| | Probing the Delicate Balance Between Pauli Repulsion and London Dispersion with Triphenylmethyl Derivatives | Q56981305 |
| | Synthesis of Substituted Adamantylzinc Reagents Using a Mg-Insertion in the Presence of ZnCl2 and Further Functionalizations | Q57742541 |
| | Stable Alkanes Containing Very Long Carbon–Carbon Bonds | Q57742615 |
| P577 | publication date | 2020-02-17 | |
| P1433 | published in | Angewandte Chemie International Edition | Q62023953 |
| P1476 | title | Selective ortho-Functionalization of Adamantylarenes Enabled by Dispersion and an Air-Stable Palladium(I) Dimer | |