SUBSTITUTED 8-METHOXYQUINOLINES - REGIOSELECTIVE BROMINATION, COUPLING REACTIONS AND CYCLIZATION TO AN 11H-INDOLO[3,2-C]QUINOLINE

Authors
TRECOURT F MONGIN F MALLET M QUEGUINER G
Citation
F. Trecourt et al., SUBSTITUTED 8-METHOXYQUINOLINES - REGIOSELECTIVE BROMINATION, COUPLING REACTIONS AND CYCLIZATION TO AN 11H-INDOLO[3,2-C]QUINOLINE, Synthetic communications, 25(24), 1995, pp. 4011-4024
Citations number
20
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Synthetic communications → ACNP
ISSN journal
00397911
Volume
25
Issue
24
Year of publication
1995
Pages
4011 - 4024
Database
ISI
SICI code
0039-7911(1995)25:24<4011:S8-RBC>2.0.ZU;2-N
Abstract
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.