Substituted 8-methoxyquinolines: Regioselective bromination, coupling reactions and cyclization to an 11H-indolo[3,2-c]quinoline

Article abstract of DOI:10.1080/00397919508011477

5,7-Disubstituted 8-methoxyquinolines were brominated at C-3 position. The palladium-catalyzed cross-coupling of obtained 3-bromoquinolines with phenylboric acids gave corresponding 3-arylquinolines from which a substituted 11H-indolo[3,2-c]quinoline could be synthesized.

Full text of DOI:10.1080/00397919508011477

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Synthetic Communications: An
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Substituted 8-
Methoxyquinolines:
Regioselective Bromination,
Coupling Reactions and
Cyclization to an 11H-
Indolo[3,2-C]quinoline
Francois Trécourt a , Florence Mongin a , Marc Mallet
a & Guy Quéguiner a
a Laboratoire de Chimie Organique Fine et
Hétérocyclique de l′IRCOF, URA CNRS 1429 Institut
National des Sciences Appliquées de Rouen , BP 08,
76131, Mont-Saint-Aignan, Cedex, France
Published online: 23 Sep 2006.
To cite this article: Francois Trécourt , Florence Mongin , Marc Mallet & Guy
Quéguiner (1995) Substituted 8-Methoxyquinolines: Regioselective Bromination,
Coupling Reactions and Cyclization to an 11H-Indolo[3,2-C]quinoline, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 25:24, 4011-4024, DOI: 10.1080/00397919508011477
To link to this article: http://dx.doi.org/10.1080/00397919508011477
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