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Generating Cu(II)-oxyl/Cu(III)-oxo species from Cu(I)-alpha-ketocarboxylate complexes and O2: in silico studies on ligand effects and C-H-activation reactivity.Copper(I)-alpha-ketocarboxylate complexes: characterization and O2 reactions that yield copper-oxygen intermediates capable of hydroxylating arenesMultiple Multidentate Halogen Bonding in Solution, in the Solid State, and in the (Calculated) Gas Phase.Reduction of nitrous oxide to dinitrogen by a mixed valent tricopper-disulfido cluster.Carbon-Halogen Bond Activation by Selenium-Based Chalcogen Bonding.Isothermal calorimetric titrations on charge-assisted halogen bonds: role of entropy, counterions, solvent, and temperature.Characterizing the interplay of Pauli repulsion, electrostatics, dispersion and charge transfer in halogen bonding with energy decomposition analysis.The 3rd Transatlantic Frontiers in Chemistry Symposium.Nucleophilic beta-oniovinylation: concept, mechanism, scope, and applications.Catalytic Carbon-Chlorine Bond Activation by Selenium-Based Chalcogen Bond Donors.A halogen-bonding-catalyzed Michael addition reaction.Synthesis of Polyflourinated Biphenyls; Pushing the Boundaries of Suzuki-Miyaura Cross Coupling with Electron-Poor Substrates.The Interaction Modes of Haloimidazolium Salts in Solution.Halogen Bonding in Organic Synthesis and Organocatalysis.Iodine(III) derivatives as halogen bonding organocatalysts.Activation of glycosyl halides by halogen bonding.Enantioselective reduction of sulfur-containing cyclic imines through biocatalysis.The role of charge in 1,2,3-triazol(ium)-based halogen bonding activators.What Active Space Adequately Describes Oxygen Activation by a Late Transition Metal? CASPT2 and RASPT2 Applied to Intermediates from the Reaction of O2with a Cu(I)-α-KetocarboxylateRefined SMD Parameters for Bromine and Iodine Accurately Model Halogen-Bonding Interactions in SolutionOn the directionality of halogen bondingUnexpected trends in halogen-bond based noncovalent adductsCatalytic deracemization of chiral allenes by sensitized excitation with visible lightChiral Propargylic Cations as Intermediates in SN1-Type Reactions: Substitution Pattern, Nuclear Magnetic Resonance Studies, and Origin of the DiastereoselectivityDiastereotopos-Differentiation in the Rh-Catalyzed Amination of Benzylic Methylene Groups in the α-Position to a Stereogenic CenterEnantio- and Regioselective Epoxidation of Olefinic Double Bonds in Quinolones, Pyridones, and Amides Catalyzed by a Ruthenium Porphyrin Catalyst with a Hydrogen Bonding SiteStructure, stereoelectronics, and synthetic potential of 1,2-bisonio-1,2-bis(dialkylamino)ethenes4,4'-Azobis(halopyridinium) derivatives: strong multidentate halogen-bond donors with a redox-active coreIron catalysis for in situ regeneration of oxidized cofactors by activation and reduction of molecular oxygen: a synthetic metalloporphyrin as a biomimetic NAD(P)H oxidaseHalogen-bond-induced activation of a carbon-heteroatom bond5-Iodo-1,2,3-triazolium-based multidentate halogen-bond donors as activating reagentsUnderstanding, controlling and programming cooperativity in self-assembled polynuclear complexes in solutionToward molecular recognition: three-point halogen bonding in the solid state and in solutionCationic Multidentate Halogen-Bond Donors in Halide Abstraction Organocatalysis: Catalyst Optimization by PreorganizationPotent affinity material for tracing acetone and related analytes based on molecular recognition by halogen bondsCorrigendum: Multiple Multidentate Halogen Bonding in Solution, in the Solid State, and in the (Calculated) Gas PhaseActivation of a carbonyl compound by halogen bondingBidentate Chiral Bis(imidazolium)-Based Halogen-Bond Donors: Synthesis and Applications in Enantioselective Recognition and CatalysisPreorganization: A Powerful Tool in Intermolecular Halogen Bonding in SolutionChalcogen Bonding Catalysis of a Nitro-Michael Reaction
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description
hulumtues
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researcher
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wetenschapper
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հետազոտող
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name
Stefan M Huber
@ast
Stefan M Huber
@en
Stefan M Huber
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Stefan M Huber
@nl
Stefan M Huber
@sl
type
label
Stefan M Huber
@ast
Stefan M Huber
@en
Stefan M Huber
@es
Stefan M Huber
@nl
Stefan M Huber
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altLabel
Stefan M. Huber
@en
prefLabel
Stefan M Huber
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Stefan M Huber
@en
Stefan M Huber
@es
Stefan M Huber
@nl
Stefan M Huber
@sl
P1053
F-7660-2011
P106
P21
P31
P3829
P496
0000-0002-4125-159X