Original and efficient synthesis of substituted 3,4-dihydronaphtho[2,3-g] quinoline-2,6,11(1H)-triones

Synthesis

Volumn , Issue 21, 2009, Pages 3677-3683

  Khoumeri, Omar ^a   Terme, Thierry ^a   Vanelle, Patrice ^a  

^a AIX MARSEILLE UNIVERSITY   (France)

Author keywords

Cyclization; Electron transfer; Malonate; Naphthoquinolinetriones; Quinones

Indexed keywords

CYCLIZATION REACTIONS; EFFICIENT SYNTHESIS; ELECTRON TRANSFER; MALONATE; MALONATES; ONE POT; TETRAKIS(DIMETHYL-AMINO)ETHYLENE;

ELECTRON TRANSITIONS; ETHYLENE; SYNTHESIS (CHEMICAL);

CYCLIZATION;

2 (BROMOMETHYL) 1,4 DIMETHOXY 9,10 ANTHRAQUINONE; 3 HYDROXY 5,12 DIMETHOXY 3 METHYL 3,4 DIHYDRONAPHTHO[2,3 G]QUINOLINE 2,6,11(11H) TRIONE; 3,12 DIHYDROXY 5 METHOXY 3 METHY 3,4 DIHYDRONAPHTHO[2,3 G]QUINOLINE 2,6,11(1H) TRIONE; 3,12 DIHYDROXY 5 METHOXY 3,4 DIHYDRONAPHTHO[2,3 G]QUINOLINE 2,6,11(1H) TRIONE; ANTHRAQUINONE DERIVATIVE; DIETHYL 2 [(1,4 DIMETHOXY 3 NITRO 9,10 DIOXO 9,10 DIHYDROANTHRACEN 2 YL)METHYL](HYDROXY)MALONATE; DIETHYL [(1,4 DIMETHOXY 3 NITRO 9,10 DIOXO 9,10 DIHYDROANTHRACEN 2 YL)METHYL](METHYL)MALONATE; DIETHYL [(1,4 DIMETHOXY 3 NITRO 9,10 DIOXO 9,10 DIHYDROANTHRACEN 2 YL)METHYL](PHENYL)MALONATE; DIETHYL [(1,4 DIMETHOXY 3 NITRO 9,10 DIOXO 9,10 DIHYDROANTHRACEN 2 YL)METHYL]MALONATE; DIETHYL [(1,4 DIMETHOXY 9,10 DIOXO 9,10 DIHYDROANTHRACEN 2 YL)METHYL](HYDROXY)MALONATE; DIETHYL HYDROXY [(4 HYDROXY 1 METHOXY 3 NITRO 9,10 DIOXO 9,10 DIHYDROANTHRACEN 2 YL)METHYL]MALONATE; DIMETHYL [(1,4 DIMETHOXY 3 NITRO 9,10 DIOXO 9,10 DIHYDROANTHRACEN 2 YL)METHYL]MALONATE; ETHYL 2 HYDROXY 3 (4 HYDROXY 1 METHOXY 3 NITRO 9,10 DIOXO 9,10 DIHYDROANTHRACEN 2 YL) 2 METHYLPROPANOATE; ETHYL 2 HYDROXY 3 (4 HYDROXY 1 METHOXY 3 NITRO 9,10 DIOXO 9,10 DIHYDROANTHRACEN 2 YL)PROPANOATE; ETHYL 3 (1,4 DIMETHOXY 3 NITRO 9,10 DIOXO 9,10 DIHYDROANTHRACEN 2 YL) 2 HYDROXY 2 METHYL PROPANOATE; ETHYL 3 (1,4 DIMETHOXY 9,10 DIHYDROANTHRACEN 2 YL) 2 HYDROXYPROPANOATE; ETHYL 3 (1,4 DIMETHOXY 9,10 DIOXO 9,10 DIHYDROANTHRACEN 2 YL) 2 HYDROXY 2 METHYLPROPANOATE; ETHYL 3 HYDROXY 5,12 DIMETHOXY 2,6,11 TRIOXO 1,2,3,4,6,11 HEXAHYDRONAPHTHO[2,3 G]QUINOLINE 3 CARBOXYLATE; ETHYL 3,12 DIHYDROXY 5 METHOXY 2,7,11 TRIOXO 1,2,3,4,6,11 HEXAHYDRONAPHTHO[2,3 G]QUINOLINE 3 CARBOXYLATE; ETHYL 5,12 DIMETHOXY 2,6,11 TRIOXO 1,2,3,4,6,11 HEXAHYDRONAPHTHO[2,3 G]QUINOLINE 3 CARBOXYLATE; ETHYL 5,12 DIMETHOXY 2,6,11 TRIOXO 3 PHENYL 1,2,3,4,6,11 HEXAHYDRONAPHTHO[2,3 G]QUINOLINE 3 CARBOXYLATE; ETHYL 5,12 DIMETHOXY 3 METHYL 2,6,11 TRIOXO 1,2,3,4,6,11 HEXAHYDRONAPHTHO[2,3 G]QUINOLINE 3 CARBOXYLATE; MALONIC ACID; METHYL 5,12 DIMETHOXY 2,6,11 TRIOXO 1,2,3,4,6,11 HEXAHYDRONAPHTHO[2,3 G]QUINOLINE 3 CARBOXYLATE; UNCLASSIFIED DRUG;

ARTICLE; CYCLIZATION; DEMETHYLATION; DRUG SYNTHESIS; ONE POT SYNTHESIS; REDUCTION; SUBSTITUTION REACTION;

EID: 72049119392     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0029-1217001     Document Type: Article

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