Halogenated quinolines as substrates for the palladium-catalyzed cross-coupling reactions to afford substituted quinolines

Journal of Heterocyclic Chemistry

Volumn 50, Issue 1, 2013, Pages 1-16

  Mphahlele, Malose J ^a   Lesenyeho, Lehlohonolo G ^a  

^a UNIVERSITY OF SOUTH AFRICA   (South Africa)

Author keywords

[No Author keywords available]

Indexed keywords

2 (4 CHLOROPHENYL) 4 IODOQUINOLINE; 2 ALKOXY 7 BROMOQUINOLINE; 2 ALKYNYL 4 ARYLQUINOLINE; 2 CHLOROQUINOLINE; 2 METHYL 4 PHENYLETHYLENYLQUINOLINE; 2,6 DIBROMOQUINOLINE; 3 FORMYL 2 IODOQUINOLINE; 3,6 DIARYL 4,7 DICHLOROQUINOLINE; 4 (2 ARYLVINYL) 8 HYDROXYQUINOLINE; 4 (2 ARYLVINYL) 8 TOSYLOXYQUINOLINE; 4 (2 METHYLPHENYLAMINO) 3 IODOQUINOLINE; 4 HALOQUINOLINE; 4 PHENYLETHYNYLQUINOLINE; 4 PHENYLQUINOLINE; 6 BROMO 2 METHOXYQUINOLINE; 6 BROMO 4,7 DICHLORO 3 IODOQUINOLINE; 8 BROMOQUINOLINE; ANTIMITOTIC AGENT; CHLOROQUINE; N,N DIMETHYLFORMAMIDE; PALLADIUM COMPLEX; QUINOLINE DERIVATIVE; TETRAHYDROFURAN; UNCLASSIFIED DRUG; ZINC CHLORIDE;

ANTIPROLIFERATIVE ACTIVITY; CATALYSIS; COVALENT BOND; CROSS COUPLING REACTION; GRIGNARD REACTION; HALOGENATION; HECK REACTION; HETERONUCLEAR MULTIPLE BOND CORRELATION; HIYAMA REACTION; HUMAN; KUMADA REACTION; MICROWAVE IRRADIATION; NEGISHI REACTION; ONE POT SYNTHESIS; REVIEW; SOLID TUMOR; SONOGASHIRA REACTION; STILLE REACTION; SUZUKI REACTION;

EID: 84873818008     PISSN: 0022152X     EISSN: 19435193     Source Type: Journal    
DOI: 10.1002/jhet.932     Document Type: Review

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