Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5281358 | Tetrahedron Letters | 2010 | 5 Pages |
Abstract
One-pot efficient synthesis of functionalized 5,6-dihydropyran-2-ones has been delineated by reacting 2H-pyran-2-ones and acetol in the presence of a base at room temperature. The formation of 5,6-dihydropyran-2-ones revealed that the reaction proceeded in a unique ‘ring transformation-rearrangement’ sequence.
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