Highly efficient and mild copper-catalyzed N- and C-arylations with aryl bromides and iodides

Chemistry - A European Journal

Volumn 10, Issue 22, 2004, Pages 5607-5622

  Cristau, Henri Jean ^a   Cellier, Pascal P ^a,c   Spindler, Jean Francis ^b   Taillefer, Marc ^a  

^a Laboratoire de Chimie Macromoleculaire UMR 5076   (France)

^b Rhodia Europe   (France)

^c CNRS   (France)

Author keywords

Arylation; Copper; Homogeneous catalysis; N,O ligands; Nucleophilic substitution

Indexed keywords

CATALYST ACTIVITY; CATALYST SELECTIVITY; COMPLEXATION; CONDENSATION; DERIVATIVES; NITROGEN COMPOUNDS;

C-ARYLATION; IMIDAZOLE; N-ARYLATION; NITROGEN HETEROCYCLES;

COPPER;

BROMIDE; COPPER; IODIDE; MALONIC ACID DERIVATIVE; NATURAL PRODUCT; SCHIFF BASE; TRANSITION ELEMENT;

ANALYTIC METHOD; ARTICLE; ARYLATION; CATALYSIS; CHEMICAL REACTION; COMPLEX FORMATION; COUPLING FACTOR; DERIVATIZATION; REACTION ANALYSIS; RELIABILITY; SOLUBILITY; STOICHIOMETRY; STRUCTURE ANALYSIS;

EID: 9244225109     PISSN: 09476539     EISSN: None     Source Type: Journal    
DOI: 10.1002/chem.200400582     Document Type: Article

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