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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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Synthesis of conformationally constrained peptidomimetics using multicomponent reactions.

TL;DR: A novel modular synthetic approach toward constrained peptidomimetics that involves a highly efficient three-step sequence including two multicomponent reactions, thus allowing unprecedented diversification of both the peptide moieties and the turn-inducing scaffold is reported.
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2-(2′-Pyridyl)-4,6-diphenylphosphinine versus 2-(2′-pyridyl)-4,6-diphenylpyridine: an evaluation of their coordination chemistry towards Rh(I)

TL;DR: The coordination chemistry of the bidentate P,N hybrid ligand 2-(2′-pyridyl)-4,6-diphenylphosphinine towards Rh(I) has been investigated and compared to the structurally analogous 2,2′ bipyridine derivative as mentioned in this paper.
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Cyclometalated Phosphinine–Iridium(III) Complexes: Synthesis, Reactivity, and Application as Phosphorus-Containing Water-Oxidation Catalysts

TL;DR: In this article, the first phosphorus-containing Ir(III) complex was synthesized by chloride abstraction from [Cp*Ir(P∧C)Cl] with AgOSO2CF3SO3 and crystallographically characterized.

Three new asymmetric trans-amine(azole)dichloridoplatinum complexes that overcome cisplatin resistance and their reactions with 5'-GMP

TL;DR: In this paper, three asymmetric platinum(II) complexes comprising an isopropylamine ligand trans to an azole ligand were synthesized and fully characterized by (1)H NMR, (195)Pt NMR and IR and elemental analysis.
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Reactions of Pyridyl-Functionalized, Chelating λ3-Phosphinines in the Coordination Environment of RhIII and IrIII

TL;DR: These new transformations in the coordination environment of Rh( III) and Ir(III) provide an easy and general access to new transition-metal complexes containing λ(5)σ(4)-phosphinine ligands.