| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5222539 | Tetrahedron | 2011 | 6 Pages |
Abstract
The Biginelli 3,4-dihydropyrimidin-2(1H)-one was converted to various C2-multifunctionalized pyrimidines via the dehydrogenation and Mitsunobu reaction using amines, alcohols, phenols and carboxylic acids as nucleophiles. A possible mechanism was also proposed to rationalize the formation of products.
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