Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5227502 | Tetrahedron | 2006 | 9 Pages |
Abstract
Synthesis of novel thiazoloindolo[3,2-c]quinoline and 8-substituted-11H-indolo[3,2-c]quinolines was performed via Graebe-Ullmann thermal cyclization from appropriated N-arylated benzotriazoles. 7H-4,7-Diaza-benzo[de]anthracene, a by-product reaction structurally closed to pyridoacridine skeleton was also identified.
The synthesis of original thiazoloindolo[3,2-c]quinoline and quinolinoquinoline rings system was investigated from benzotriazoles following a microwave-assisted Graebe-Ullmann cyclization.Download full-size image
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Authors
Anne Beauchard, Hadjila Chabane, Sourisak Sinbandhit, Pierre Guenot, Valérie Thiéry, Thierry Besson,