| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5269486 | Tetrahedron Letters | 2014 | 6 Pages |
Abstract
The one-pot reactions of aryl glyoxals with acetylacetone and urea using molybdate sulfuric acid (5 mol %) lead to the novel functionalized 5-acetyl-4-(aryloyl)-3,4-dihydropyrimidinones, which readily undergo the Knorr condensation with hydrazines to produce new pyrimido[4,5-d]pyridazines. The present strategies are in accordance with green chemistry principles through the use of a safe and recyclable catalyst under solvent-free conditions.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Bahador Karami, Saeed Khodabakhshi, Sedigheh Akrami, Mahnaz Farahi,