| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5221807 | Tetrahedron | 2011 | 5 Pages |
Abstract
A facile and efficient synthesis of fully substituted pyridin-2(1H)-ones has been developed by the reaction of readily available α-oxoketene-S,S-acetals with malononitrile in the presence of sodium methoxide in methanol under reflux.
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