Supramolecular catalysis. Part 1: non-covalent interactions as a tool for building and modifying homogeneous catalysts.
about
Reversible manipulation of the G-quadruplex structures and enzymatic reactions through supramolecular host-guest interactionsMacrocyclic shape-persistency of cyclo[6]aramide results in enhanced multipoint recognition for the highly efficient template-directed synthesis of rotaxanes.Self-Assembly of a Library of Polyborate Chiral Anions for Asymmetric Catalytic Quinoline Reduction.Crystal structure of a mononuclear Ru(II) complex with a back-to-back terpyridine ligand: [RuCl(bpy)(tpy-tpy)](.).A concerted two-prong approach to the in situ allosteric regulation of bifunctional catalysis.Supramolecular catalysis. Part 2: artificial enzyme mimics.Gated molecular baskets.Self-Assembled Chiral Nanostructures as Scaffolds for Asymmetric Reactions.The Cation-π Interaction in Small-Molecule Catalysis.Polyaromatic N-heterocyclic carbene ligands and π-stacking. Catalytic consequences.Spontaneous Si-C bond cleavage in (TriphosSi)-nickel complexes.Short Self-Assembling Peptides Are Able to Bind to Copper and Activate OxygenStabilization of 2,6-Diarylanilinum Cation by Through-Space Cation-π Interactions.Harnessing non-covalent interactions to exert control over regioselectivity and site-selectivity in catalytic reactions.Radical polymerization by a supramolecular catalyst: cyclodextrin with a RAFT reagent.Tailored oxido-vanadium(V) cage complexes for selective sulfoxidation in confined spaces.Rhodium, iridium and nickel complexes with a 1,3,5-triphenylbenzene tris-MIC ligand. Study of the electronic properties and catalytic activities.meta-Selective C-H Borylation of Benzylamine-, Phenethylamine-, and Phenylpropylamine-Derived Amides Enabled by a Single Anionic Ligand.Aromatic Interactions in Organocatalyst Design: Augmenting Selectivity Reversal in Iminium Ion Activation.Exploiting non-covalent π interactions for catalyst design.Efficient active-template synthesis of calix[6]arene-based oriented pseudorotaxanes and rotaxanes.Nickel-Cornered Molecular Rectangles as Polycyclic Aromatic Hydrocarbon Receptors.Palladium-Catalysed Cross-Coupling Reactions Controlled by Noncovalent Zn⋅⋅⋅N Interactions.Chiral Phosphate in Rhodium-Catalyzed Asymmetric [2+2+2] Cycloaddition: Ligand, Counterion, or Both?Cyclodextrin-based PNN supramolecular assemblies: a new class of pincer-type ligands for aqueous organometallic catalysis.Air-oxidation from sulfur to sulfone-bridged Schiff-base macrocyclic complexes showing enhanced antimicrobial activities."Breathing" Motion of a Modulable Molecular Cavity.Large-Scale Synthesis of Enantiopure Molecular Cages: Chiroptical and Recognition Properties.Confinement induced thermodynamic and kinetic facilitation of some Diels-Alder reactions inside a CB[7] cavitand.De novo endo-functionalized organic cages as cooperative multi-hydrogen-bond-donating catalysts.Ligand-Substrate Dispersion Facilitates the Copper-Catalyzed Hydroamination of Unactivated Olefins.Supramolecular bidentate phosphine ligand scaffolds from deconstructed Hamilton receptors.Controlling ligand binding for tunable and switchable catalysis: cation-modulated hemilability in pincer-crown ether ligands.Gold(I) Metallo-Tweezers for the Recognition of Functionalized Polycyclic Aromatic Hydrocarbons by Combined π-π Stacking and H-Bonding.Chiral organocatalysts based on lipopeptide micelles for aldol reactions in water.Hydroformylation of Alkenes in a Planetary Ball Mill: from Additive-Controlled Reactivity to Supramolecular Control of Regioselectivity.Rational Optimization of Supramolecular Catalysts for the Rhodium-Catalyzed Asymmetric Hydrogenation Reaction.Controlling orthogonal self-assembly through cis-trans isomerization of a non-covalent palladium complex dimer.Tuning the structure of 1,3,5-benzene tricarboxamide self-assemblies through stereochemistry.Platinum-Based Organometallic Folders for the Recognition of Electron-Deficient Aromatic Substrates.
P2860
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P2860
Supramolecular catalysis. Part 1: non-covalent interactions as a tool for building and modifying homogeneous catalysts.
description
2013 nî lūn-bûn
@nan
2013 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
Supramolecular catalysis. Part ...... difying homogeneous catalysts.
@ast
Supramolecular catalysis. Part ...... difying homogeneous catalysts.
@en
type
label
Supramolecular catalysis. Part ...... difying homogeneous catalysts.
@ast
Supramolecular catalysis. Part ...... difying homogeneous catalysts.
@en
prefLabel
Supramolecular catalysis. Part ...... difying homogeneous catalysts.
@ast
Supramolecular catalysis. Part ...... difying homogeneous catalysts.
@en
P50
P356
P1476
Supramolecular catalysis. Part ...... difying homogeneous catalysts.
@en
P2093
Piet W N M van Leeuwen
P304
P356
10.1039/C3CS60027K
P577
2013-12-20T00:00:00Z