| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 5283559 | Tetrahedron Letters | 2006 | 4 Pages | 
Abstract
												Pyridopyrimidine-spirocyclohexanetriones (5, 6) and pyrimido[4,5-b]quinolinones (8) were obtained in a three-component microwave-assisted reaction of 6-aminopyrimidin-4-ones (1) with dimedone (2) and formaldehyde solution or paraformaldehyde, respectively. A mechanism is proposed based on the presence of a basic catalyst (triethylamine in this case) and the fact that single condensation intermediates are isolated prior to the cyclization leading to the final products.
											Keywords
												
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													Physical Sciences and Engineering
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											Authors
												Jairo Quiroga, Silvia Cruz, Braulio Insuasty, Rodrigo AbonÃa, Manuel Nogueras, Justo Cobo, 
											