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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Reactivity of a Ruthenium-Carbonyl Complex in the Methanol Dehydrogenation Reaction.
TL;DR: The ruthenium complex Ru(sal binapht)(CO)(Pi‐Pr3) {salbinapht=2‐[({2‐hydroxybenzyl)amino]‐[1,1′‐binaphthalen]‐2‐yl}imino)methyl]phenolato} catalyzes the methanol dehydrogenation reaction in the presence of base and water to yield H2, formate, and carbonate.
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Dynamische kombinatorische Chemie: die überraschende Rezeptorwahl durch Gastmoleküle
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Effect of Ortho Substituents on the Direction of 1,2-Migrations in the Rearrangement of 2-exo-Arylfenchyl Alcohols
TL;DR: A series of 2-exo-arylfenchyl alcohols (11a−k) was submitted to acid hydrolysis in EtOH/10 M HCl (2:1−1:1, v/v) or with trifluoromethanesulfonic acid (TfOH) (1 equiv) in CHCl3 under varying conditions.
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Reductive Elimination at an Ortho-Metalated Iridium(III) Hydride Bearing a Tripodal Tetraphosphorus Ligand
Yann Gloaguen,Lianne M. Jongens,Joost N. H. Reek,Martin Lutz,Bas de Bruin,Jarl Ivar van der Vlugt +5 more
TL;DR: In this paper, the synthesis of a tetradentate C3-symmetric tripodal, tetradate ligand with only phosphorus atoms as donor groups was described, starting from commercially available o-tolyldiphenylphosphine, and its molecular structure was determined by X-ray crystallographic analysis.
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Carbosilane Dendrimeric Carbodiimides: Site Isolation as a Lactamization Tool
A. Amore,R. van Heerbeek,N. Zeep,J. H van Esch,J.N.H. Reek,JH van Maarseeen,Joost N. H. Reek,Jan H. van Maarseveen +7 more
TL;DR: The convergent syntheses of three generations of carbosilane dendrimeric carbodiimides showed that only the first generation self-aggregates via hydrogen bonding, while the second and the third do not, implying isolation of core-bound moieties.