Copper(I) iodide catalyzed synthesis of quinolinones via cascade reactions of 2-halobenzocarbonyls with 2-arylacetamides

Synthesis

Volumn , Issue 10, 2011, Pages 1547-1554

  Fu, Liangbing ^a,b   Huang, Xiaoli ^a,b   Wang, Deping ^a,b   Zhao, Pinghua ^c   Ding, Ke ^a  

^a GUANGZHOU INSTITUTES OF BIOMEDICINE AND HEALTH   (China)

^b UNIVERSITY OF CHINESE ACADEMY OF SCIENCES   (China)

^c GAC ChangFeng Motor Co Ltd   (China)

Author keywords

amidation; cascade reactions; copper iodide; diamines; quinolinones

Indexed keywords

AMIDATION; CASCADE REACTIONS; COPPER IODIDE; DIAMINES; QUINOLINONES;

CATALYSIS; SYNTHESIS (CHEMICAL);

COPPER;

1 CYCLOPROPYL 4 METHYL 3 PHENYLQUINOLIN 2 (1H) ONE; 2 ARYLACETAMIDE DERIVATIVE; 2 HALOBENZOCARBONYL; 3 (4 FLUOROPHENYL) 4 METHYLQUINOLIN 2 (1H) ONE; 3 PHENYL 6 (TRIFLUOROMETHYL)QUINOLIN 2 (1H) ONE; 3 PHENYLQUINOLIN 2 (1H) ONE; 3,4 DIPHENYLQUINOLIN 2 (1H) ONE; 3,5,6 TRIPHENYLPYRIDIN 2 (1H) ONE; 4 AMINO 3 PHENYLQUINOLIN 2 (1H) ONE; 4 HYDROXY 3 PHENYLQUINOLIN 2 (1H) ONE; 4 METHYL 3 (1 METHYL 1H INDOL 3 YL)QUINOLIN 2 (1H) ONE; 4 METHYL 3 (4 NITROPHENYL)QUINOLIN 2 (1H) ONE; 4 METHYL 3 (PYRIDIN 2 YL)QUINOLIN 2 (1H) ONE; 4 METHYL 3 (PYRIDIN 3 YL)QUINOLIN 2 (1H) ONE; 4 METHYL 3 PHENYL 1,8 NAPHTHYRIDIN 2 (1H) ONE; 4 METHYL 3 PHENYLQUINOLIN 2 (1H) ONE; 4 METHYL 3,5,6 TRIPHENYLPYRIDIN 2 (1H) ONE; 6 CHLORO 3 PHENYLQUINOLIN 2 (1H) ONE; 6 CHLORO 3,4 DIPHENYLQUINOLIN 2 (1H) ONE; 6 CHLORO 4 METHYL 3 PHENYLQUINOLIN 2 (1H) ONE; 6 PHENYLFLUORO [3,2 B]PYRIDIN 5 (4H) ONE; 6 PHENYLTHIENO [3,2 B]PYRIDIN 5 (4H) ONE; 7 METHOXY 4 METHYL 3 PHENYLQUINOLIN 2 (1H) ONE; 7 METHYL 3 PHENYLQUINOLIN 2 (1H) ONE; 7 METHYL 6 PHENYLTHIENO [3,2 B]PYRIDIN 5 (4H) ONE; ACETOPHENONE DERIVATIVE; CUPROUS ION; HALIDE; QUINOLINE DERIVATIVE; UNCLASSIFIED DRUG;

AMIDATION; ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CATALYSIS; CHEMICAL REACTION; CHEMICAL STRUCTURE; PROTON NUCLEAR MAGNETIC RESONANCE;

EID: 79955877099     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0030-1259983     Document Type: Article

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