An expeditious approach to quinolines via Friedländer synthesis catalyzed by FeCl3 or Mg(ClO4)2

Synlett

Volumn , Issue 17, 2005, Pages 2653-2657

  Wu, Jie ^a,b   Zhang, Liang ^a   Diao, Tian Ning ^a  

^a FUDAN UNIVERSITY   (China)

^b SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY   (China)

Author keywords

Catalyst; FeCl3; Friedl nder synthesis; Mg(ClO 4)2; Quinoline

Indexed keywords

1 (2 METHYL 4 PHENYLQUINOLINE 3 YL)ETHANONE; 1 (2,4 DIMETHYLQUINOLINE 3 YL)ETHANONE; 1 (6 CHLORO 2 METHYL 4 PHENYLQUINOLIN 3 YL)ETHANONE; 1 [6 CHLORO 4 (2 CHLOROPHENYL) 2 METHYLQUINOLIN 3 YL]ETHANONE; 7 CHLORO 9 PHENYL 2,3 DIHYDRO 1H CYCLOPENTA[B]QUINOLINE; 9 PHENYL 2,3 DIHYDRO 1H CYCLOPENTA[B]QUINOLINE; 9 PHENYL 3,4 DIHYDROACRIDIN 1 (2H) ONE; CARBOXYLIC ACID DERIVATIVE; ETHYL 2 METHYL 4 PHENYLQUINOLINE 3 CARBOXYLIC ACID; ETHYL 2,4 DIMETHYLQUINOLINE 3 CARBOXYLIC ACID; ETHYL 6 CHLORO 2 METHYL 4 PHENYLQUINOLINE 3 CARBOXYLIC ACID; FERRIC CHLORIDE; MAGNESIUM PERCHLORATE; QUINOLINE DERIVATIVE; UNCLASSIFIED DRUG;

ANNULATION REACTION; ARTICLE; CATALYSIS; DRUG STRUCTURE; DRUG SYNTHESIS;

EID: 27444436217     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2005-917111     Document Type: Article

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47. 3): δ = 2.14-2.18 (m, 2 H), 2.89 (t, J = 7.3 Hz, 2 H), 3.21 (t, J = 7.8 Hz, 2 H), 7.32-7.34 (m, 2 H), 7.52-7.53 (m, 5 H), 7.98 (d, J = 9.2 Hz, 1 H) ppm.