A rational protocol for the synthesis of arylated bipyridine ligands via a cycloaddition pathway

Journal of Organic Chemistry

Volumn 72, Issue 26, 2007, Pages 10181-10193

  Diring, Stéphane ^a   Retailleau, Pascal ^b   Ziessel, Raymond ^a  

^a CNRS   (France)

^b INSTITUT DE CHIMIE DES SUBSTANCES NATURELLES   (France)

Author keywords

[No Author keywords available]

Indexed keywords

PHENYL-POLYPYRIDINE LIGANDS; TRANSITION STATE;

CHARGE TRANSFER; CYCLOADDITION; EXCITED STATES; ISOMERS; REGIOSELECTIVITY; SYNTHESIS (CHEMICAL);

LIGANDS;

ACETYLENE DERIVATIVE; ALKADIENE; BIPYRIDINE DERIVATIVE; BUTYLAMINE; ETHYLNYLGALLATE; ETHYLNYLPHENYLDIBUTYLAMINO; FUNCTIONAL GROUP; GALLIC ACID; HALOGEN; LIGAND; PALLADIUM; PARAFFIN; PLATINUM DERIVATIVE; QUINOLONE DERIVATIVE; SOLVENT; UNCLASSIFIED DRUG;

ARTICLE; ARYLATION; CATALYSIS; CATALYST; CROSS COUPLING REACTION; CYCLOADDITION; DIELS ALDER REACTION; ELECTROCHEMISTRY; ELECTRON; ISOMER; LIFESPAN; LUMINESCENCE; METHODOLOGY; QUANTUM YIELD; SPECTROSCOPY; SYNTHESIS; ULTRAVIOLET RADIATION;

2,2'-DIPYRIDYL; CYCLIZATION; LIGANDS; MAGNETIC RESONANCE SPECTROSCOPY; MODELS, MOLECULAR; MOLECULAR STRUCTURE; PYRIDINES; STEREOISOMERISM;

EID: 37549016818     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo7019866     Document Type: Article

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