| 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, 
											![First Page Preview: Synthesis of original thiazoloindolo[3,2-c]quinoline and novel 8-N-substituted-11H-indolo[3,2-c]quinoline derivatives from benzotriazoles. Part I Synthesis of original thiazoloindolo[3,2-c]quinoline and novel 8-N-substituted-11H-indolo[3,2-c]quinoline derivatives from benzotriazoles. Part I](/preview/png/5227502.png)