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Martin Lutz

Researcher at Utrecht University

Publications -  595
Citations -  18692

Martin Lutz is an academic researcher from Utrecht University. The author has contributed to research in topics: Ligand & Catalysis. The author has an hindex of 62, co-authored 592 publications receiving 17289 citations. Previous affiliations of Martin Lutz include University of Amsterdam & ETH Zurich.

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Diastereoselective self-assembly of chiral diamine-chelated aryllithiums to dimeric aggregates.

TL;DR: X-ray crystallographic studies and molecular weight determinations by cryoscopy in benzene showed that, both in the solid state and in apolar, noncoordinating solvents such as benzene, these compounds exist as discrete dimeric aggregates.
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Maleic anhydride, redetermination at 130 K

TL;DR: The X-ray crystal structure of 2,5-furan-dione (C4H2O3) was determined at 130'2' K as discussed by the authors, which is the standard.
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2,4,6-Triarylphosphinines versus 2,4,6-triarylpyridines: an investigation of the differences in reactivity between structurally related aromatic phosphorus and nitrogen heterocycles.

TL;DR: Although 2,4,6-triarylphosphinines undergo facile CH activation with [Cp*IrCl2 ]2 in the presence of NaOAc, this reaction does not proceed with the corresponding pyridine derivatives, and the treatment of phosphinines with Pd(OAc)2 led to the formation of the unusual cofacial oxidative coupling products 16 and 17, which consist of a phosphorus-containing cage structure.
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Development of a benzimidazole-derived bidentate P,N-ligand for enantioselective iridium-catalyzed hydrogenations

TL;DR: In this paper, a benzimidazole-derived bidentate P,N-ligand and its application in Ir-catalyzed hydrogenation was described, where the ligand backbone was obtained through a one-pot tandem hydroformylation-cyclization sequence and the enantiomers of the generated alcohol were separated by chiral HPLC.
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Intermolecular C-H activation with an Ir-METAMORPhos piano-stool complex--multiple reaction steps at a reactive ligand.

TL;DR: A stoichiometric anti-Markovnikov C-N bond formation involving ligand reactivity in multiple steps along the reaction coordinate is described, which affords a highly unusual four-membered iridacycle bearing an exo-cyclic C=C double bond.