Highly efficient and mild copper-catalyzed N- and C-arylations with aryl bromides and iodides.
about
Structures, reactivities, and antibiotic properties of the marinopyrroles A-FComputational explorations of mechanisms and ligand-directed selectivities of copper-catalyzed Ullmann-type reactions.Heterogeneous Cu(II) -catalysed solvent-controlled selective N-arylation of cyclic amides and amines with bromo-iodoarenes.Cobalt-catalyzed intermolecular C(sp(2))-O cross-coupling.Completely N1-selective palladium-catalyzed arylation of unsymmetric imidazoles: application to the synthesis of nilotinibDiamine Ligands in Copper-Catalyzed Reactions.Optimization of the central heterocycle of alpha-ketoheterocycle inhibitors of fatty acid amide hydrolase.Photo-induced oxidant-free oxidative C-H/N-H cross-coupling between arenes and azoles.Advances in copper-catalyzed C-C coupling reactions and related domino reactions based on active methylene compounds.Polymers for electronics and spintronics.Copper catalysed Ullmann type chemistry: from mechanistic aspects to modern development.Copper-mediated aromatic amination reaction and its application to the total synthesis of natural products.Oxidative Coupling of Aryl Boron Reagents with sp(3)-Carbon Nucleophiles: The Enolate Chan-Evans-Lam Reaction.Charge-tagged ligands: useful tools for immobilising complexes and detecting reaction species during catalysis.Synthesis and biological activities of azalamellarins.4,4'-Bis(benzimidazol-1-yl)biphen-ylA Cu-Catalysed Radical Cross-Dehydrogenative Coupling Approach to Acridanes and Related Heterocycles.New efficient ligand for sub-mol % copper-catalyzed C-N cross-coupling reactions running under air.High catalytic activity of oriented 2.0.0 copper(I) oxide grown on graphene film.Copper complexes of anionic nitrogen ligands in the amidation and imidation of aryl halides.Copper(I) enolate complexes in α-arylation reactions: synthesis, reactivity, and mechanismAn organocatalytic route to 2-heteroarylmethylene decorated N-arylpyrroles.Discriminating role of bases in diketonate copper(I)-catalyzed C-O couplings: phenol versus diarylether.Mechanism of the Ullmann Biaryl Ether Synthesis Catalyzed by Complexes of Anionic Ligands. Evidence for the Reaction of Iodoarenes With Ligated Anionic CuI Intermediates.Alcohol assisted C-C bond breaking: copper-catalyzed deacetylative α-arylation of β-keto esters and amides.Picolinamides as effective ligands for copper-catalysed aryl ether formation: structure-activity relationships, substrate scope and mechanistic investigations.Copper-catalyzed arylation of nitrogen heterocycles from anilines under ligand-free conditions.Room-temperature Cu-catalyzed N-arylation of aliphatic amines in neat water.Micro/milliflow processing with selective catalyst microwave heating in the Cu-catalyzed Ullmann etherification reaction: a μ(2)-process.K-Region-Extended [c]-Heteroannulated Pyrenes.Reaction mechanisms of carbon dioxide, ethylene oxide and amines catalyzed by ionic liquids BmimBr and BmimOAc: a DFT study.A new mild synthetic route to N-arylated pyridazinones from aryldiazonium salts.α-Haloacrylates as acceptors in the [3 + 2] cycloaddition reaction with NaN3: an expedient approach to N-unsubstituted 1,2,3-triazole-4-carboxylates.Copper/N,N-dimethylglycine catalyzed goldberg reactions between aryl bromides and amides, aryl iodides and secondary acyclic amides.Base-free Knoevenagel condensation catalyzed by copper metal surfaces.Green alternative solvents for the copper-catalysed arylation of phenols and amidesCopper Catalyzed Assembly ofN-Aryloxazolidinones: Synthesis of Linezolid, Tedizolid, and RivaroxabanA straightforward one-pot synthesis of bioactive N-aryl oxazolidin-2-ones via a highly efficient Fe3O4@SiO2-supported acetate-based butylimidazolium ionic liquid nanocatalyst under metal- and solvent-free conditionsEfficacy of C-N Coupling Reactions with a New Multinuclear Copper Complex Catalyst and Its Dissociation into Mononuclear SpeciesMesoporous nitrogen-doped carbon for copper-mediated Ullmann-type C–O/–N/–S cross-coupling reactions
P2860
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P2860
Highly efficient and mild copper-catalyzed N- and C-arylations with aryl bromides and iodides.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年学术文章
@wuu
2004年学术文章
@zh
2004年学术文章
@zh-cn
2004年学术文章
@zh-hans
2004年学术文章
@zh-my
2004年学术文章
@zh-sg
2004年學術文章
@yue
2004年學術文章
@zh-hant
name
Highly efficient and mild copp ...... ith aryl bromides and iodides.
@en
Highly efficient and mild copp ...... ith aryl bromides and iodides.
@nl
type
label
Highly efficient and mild copp ...... ith aryl bromides and iodides.
@en
Highly efficient and mild copp ...... ith aryl bromides and iodides.
@nl
prefLabel
Highly efficient and mild copp ...... ith aryl bromides and iodides.
@en
Highly efficient and mild copp ...... ith aryl bromides and iodides.
@nl
P2093
P356
P1476
Highly efficient and mild copp ...... ith aryl bromides and iodides.
@en
P2093
Jean-Francis Spindler
Marc Taillefer
Pascal P Cellier
P304
P356
10.1002/CHEM.200400582
P407
P577
2004-11-01T00:00:00Z