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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Liganden, die während der Katalyse Elektronen speichern und freisetzen
TL;DR: In this paper, a Cobalt-vermittelte Negishi-Kreuzkupplung bietet ein Beispiel fur dieses Konzept and verdeutlicht sein Potenzial fur die Entwicklung neuer katalytischer Reaktionen with kostengunstigen Metallen.
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Templated assembly of a molecular capsule
Joost N. H. Reek,Albertus P. H. J. Schenning,Anton W. Bosman,E. W. Meijer,Maxwell J. Crossley +4 more
TL;DR: Two rigid Troger's base dizinc(II) bis-porphyrin receptor molecules and the first generation of dendrimer tetramine 4 form a 2:1 complex as discussed by the authors.
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N–H bond activation by palladium(II) and copper(I) complexes featuring a reactive bidentate PN-ligand
TL;DR: The first examples of reactivity at the backbone of a bidentate PN-ligand L1H relevant to N-H activation are described, leading to novel Pd(II) and Cu(I) amido complexes.
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Sulfonated Xantphos Ligand and Methylated Cyclodextrin: A Winning Combination for Rhodium-Catalyzed Hydroformylation of Higher Olefins in Aqueous Medium
Loïc Leclercq,Frédéric Hapiot,Sébastien Tilloy,K. Ramkisoensing,Joost N. H. Reek,P.W.N.M. van Leeuwen,Eric Monflier +6 more
TL;DR: The potential of sulfonated xantphos as ligand for a cyclodextrin-based hydroformylation process has been investigated in this article, where an increase in the linear to branched aldehydes ratio was measured when randomly methylated α- or β-cyclodextrins were used as inverse phase-transfer catalysts.
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Beyond Classical Reactivity Patterns: Hydroformylation of Vinyl and Allyl Arenes to Valuable β- and γ-Aldehyde Intermediates Using Supramolecular Catalysis
TL;DR: It is demonstrated that this strategy allows for unprecedented reversal of selectivity to form otherwise disfavored β-aldehyde products in the hydroformylation of vinyl 2- and 3-carboxyarenes, with chemo- and regioselectivity up to 100%.