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Volumn 30, Issue 5, 2006, Pages 803-809
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Heck reaction catalysed by palladium supported with an electron-rich benzimidazolylidene generated in situ: Remarkable ligand electronic effects and controllable mono- and di-arylation
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Author keywords
[No Author keywords available]
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Indexed keywords
2 CHLOROBENZONITRILE;
2,5 DIMETHYLBROMOBENZENE;
4 CHLOROACETOPHENONE;
5,6 DIBUTOXY N,N' DIBUTYLBENZIMIDAZOLIUM BROMIDE;
5,6 DIFLUORO N,N' DIBUTYLBENZIMIDAZOLIUM BROMIDE;
ACRYLIC ACID BUTYL ESTER;
AROMATIC HYDROCARBON;
BENZIMIDAZOLE DERIVATIVE;
BENZIMIDAZOLYLIDENE;
BROMINE DERIVATIVE;
BUTYL MESITYLCINNAMATE;
CHLORIDE;
CINNAMIC ACID DERIVATIVE;
HALIDE;
IONIC LIQUID;
LIGAND;
MESITYL BROMIDE;
N,N' DIBUTYLBENZIMIDAZOLIUM BROMIDE;
PALLADIUM;
TETRABUTYLAMMONIUM;
UNCLASSIFIED DRUG;
ARTICLE;
ARYLATION;
CARBON NUCLEAR MAGNETIC RESONANCE;
CATALYSIS;
CATALYST;
GAS CHROMATOGRAPHY;
HECK REACTION;
MASS SPECTROMETRY;
PRIORITY JOURNAL;
PROTON NUCLEAR MAGNETIC RESONANCE;
STEREOSPECIFICITY;
SYNTHESIS;
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EID: 33646582636
PISSN: 11440546
EISSN: 13699261
Source Type: Journal
DOI: 10.1039/b601833e Document Type: Article |
Times cited : (51)
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References (75)
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