Synthesis of hydroxyquinoline derivatives, amino-hydroxychromene, aminocoumarin and their anti-bacterial activities

Heterocycles

Volumn 63, Issue 8, 2004, Pages 1793-1812

  Abd El Aziz, Alaa S ^a   El Agrody, Ahmed M ^a   Bedair, Ahmed H ^a   Corkery, T Christopher ^a   Ata, Athar ^a  

^a UNIVERSITY OF WINNIPEG   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

2 AMINO 6 (N HEXYL) 7 HYDROXY 4 (4 CHLOROPHENYL) 4H CHROMENE 3 CARBONITRILE; 2 AMINO 6 ETHYL 7 HYDROXY 4 (4 CHLOROPHENYL) 4H CHROMENE 3 CARBONITRILE; 2 AMINO 7 HYDROXY 4 (4 CHLOROPHENYL) 4H CHROMENE 3 CARBONITRILE; 2 AMINO 7 HYDROXY 4 (4 CHLOROPHENYL) 4H CHROMENE DERIVATIVE; 2 AMINO 7 HYDROXY 8 METHYL 4 (4 CHLOROPHENYL) 4H CHROMENE 3 CARBONITRILE; 2,7 DIAMINO 4 (4 CHLOROPHENYL) 4H CHROMENE 3 CARBONITRILE; 2,7 DIAMINO 4 (4 METHOXYPHENYL) 4H CHROMENE 3 CARBONITRILE; 2,7 DIAMINO 4 PHENYL 4H CHROMENE 3 CARBONITRILE; 3,8 DIAMINO 1 (4 CHLOROPHENYL) 1H BENZO[H]CHROMENE 2 CARBONITRILE; 3,8 DIAMINO 1 (4 METHOXYPHENYL) 1H BENZO[H]CHROMENE 2 CARBONITRILE; 3,8 DIAMINO 1 PHENYL 1H BENZO[H]CHROMENE 2 CARBONITRILE; 4 HYDROXYCOUMARIN; 7 AMINO 4 COUMARIN DERIVATIVE; 7 HYDROXY 4 (4 METHOXYPHENYL) 2 OXO 1,2 DIHYDROQUINOLINE 3 CARBONITRILE; 7 HYDROXY 4 PHENYL 2 OXO 1,2 DIHYDROQUINOLINE 3 CARBONITRILE; AMINOHYDROXYCHROMENE DERIVATIVE; AMINOPHENOL DERIVATIVE; CHROMENE DERIVATIVE; COUMARIN DERIVATIVE; CYANIDE; DIAMINOCHROMENE DERIVATIVE; ETHYL 2,7 DIAMINO 4 (4 METHOXYPHENYL) 4H CHROMENE 3 CARBOXYLATE; ETHYL 3,8 DIAMINO 1 (4 CHLOROPHENYL) 1H BENZO[H]CHROMENE 2 CARBOXYLATE; ETHYL 3,8 DIAMINO 1 (4 METHOXYPHENYL) 1H BENZO[H]CHROMENE 2 CARBOXYLATE; ETHYL 3,8 DIAMINO 1 PHENYL 1H BENZO[H]CHROMENE 2 CARBOXYLATE; NAPHTHOL DERIVATIVE; NITRILE; QUINOLINOL DERIVATIVE; RESORCINOL; UNCLASSIFIED DRUG; UNINDEXED DRUG;

ANTIBACTERIAL ACTIVITY; ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CYCLIZATION; DRUG SYNTHESIS; MICHAEL ADDITION; PROTON NUCLEAR MAGNETIC RESONANCE; REACTION ANALYSIS; STRUCTURE ACTIVITY RELATION;

EID: 4043158392     PISSN: 03855414     EISSN: None     Source Type: Journal    
DOI: 10.3987/com-04-10089     Document Type: Article

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