J
Joost N. H. Reek
Researcher at University of Amsterdam
Publications - 488
Citations - 23869
Joost N. H. Reek is an academic researcher from University of Amsterdam. The author has contributed to research in topics: Catalysis & Hydroformylation. The author has an hindex of 74, co-authored 458 publications receiving 21217 citations. Previous affiliations of Joost N. H. Reek include Wageningen University and Research Centre & Virginia Tech.
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A highly selective water-soluble dicationic palladium catalyst for the biphasic hydroxycarbonylation of alkenes
TL;DR: The application of a water-soluble diphosphine with a xanthene-type backbone in the biphasic palladium-catalysed hydroxycarbonylation reaction of alkenes leads to the selective formation of carboxylic acids.
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Hydrogen Bond Directed ortho-Selective C−H Borylation of Secondary Aromatic Amides
TL;DR: Reported is an iridium catalyst for C-H borylation of challenging secondary aromatic amide substrates, and the regioselectivity is controlled by hydrogen-bond interactions.
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Template-assisted ligand encapsulation; the impact of an unusual coordination geometry on a supramolecular pyridylphosphine-Zn(II)porphyrin assembly.
TL;DR: The tris(para-pyridyl)phosphine-porphyrin stoichiometry determined in solution (1:3) differs markedly with that observed in the solid state (2:5, for assembly [1](2).[2](5)).
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Nickel-Catalyzed Stereodivergent Synthesis of E- and Z-Alkenes by Hydrogenation of Alkynes
Kathiravan Murugesan,Charles Beromeo Bheeter,Pim R. Linnebank,Anke Spannenberg,Joost N. H. Reek,Rajenahally V. Jagadeesh,Matthias Beller +6 more
TL;DR: A convenient protocol for stereodivergent hydrogenation of alkynes to E‐ and Z‐alkenes by using nickel catalysts was developed, which was generally applicable in >40 examples and scalable to multigram‐scale experiments.
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Palladium Complexes of Phosphane-Functionalised Carbosilane Dendrimers as Catalysts in a Continuous-Flow Membrane Reactor
TL;DR: The catalytic sites at the periphery of the dendrimer support are readily accessible to the substrate as discussed by the authors, which is reflected in the high catalytic activity of the larger dendric systems.