A new synthesis of pyrrolo[3,2-b]quinolines by a tandem electrocyclization-oxidation process

Tetrahedron

Volumn 64, Issue 30-31, 2008, Pages 7266-7272

  Boisse, Thomas ^a   Gautret, Philippe ^a   Rigo, Benoît ^a   Goossens, Laurence ^b   Hénichart, Jean Pierre ^b   Gavara, Laurent ^a  

^a Ecole des Hautes Etudes d'Ingenieur   (France)

^b Faculté des Sciences Pharmaceutiques et Biologiques Université de Lille   (France)

Author keywords

Benzoazaindole; Bredereck's reagent; Electrocyclization; Methyl transfer

Indexed keywords

CARBOXYLIC ACID DERIVATIVE; DIMETHYL 1H PYRROLO[3,2 B]QUINOLINE 1,3 CARBOXYLATE; DIMETHYL 4 (1,3 BENZODIOXOL 5 YLAMINO) 2,5 DIHYDRO 1H PYRROLE 1,3 DICARBOXYLATE; DIMETHYL 4 [(2 FORMYLPHENYL)AMINO] 2,5 DIHYDRO 1H PYRROLE 1,3 DICARBOXYLATE; DIMETHYL 4[(3,4 DIMETHOXYPHENYL)AMINO] 2,5 DIHYDRO 1H PYRROLE 1,3 DICARBOXYLATE; DIMETHYL 4[(4 METHOXYPHENYL)AMINO] 2,5 DIHYDRO 1H PYRROLE 1,3 DICARBOXYLATE; DIMETHYL 4[(4 METHYLPHENYL)AMINO] 2,5 DIHYDRO 1H PYRROLE 1,3 DICARBOXYLATE; DIMETHYL 6,7 DIMETHOXY 1H PYRROLO[3,2 B]QUINOLINE 1,3 DICARBOXYLATE; DIMETHYL 7 METHOXY 1H PYRROLO[3,2 B]QUINOLINE 1,3 DICARBOXYLATE; DIMETHYL 8H [1,3]DIOXOLO[4,5 G]PYRROLO[3,2 B]QUINOLINE 6,8 DICARBOXYLATE; ETHYL 2,3 [(4 FLUOROPHENYL)AMINO]BUT 2 ENOATE; QUINOLINE DERIVATIVE;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL REACTION; CHEMICAL STRUCTURE; CYCLIZATION; OXIDATION; POLYMERIZATION; PRIORITY JOURNAL; SYNTHESIS;

EID: 45449087495     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2008.05.071     Document Type: Article

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