| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5276323 | Tetrahedron Letters | 2010 | 4 Pages |
Abstract
An unexpected reaction took place when 5-phenylthiazolidine-2,4-diones were treated in basic media to produce phenyl-α-ketoamides in good yields. The 5-phenylthiazolidine-2,4-diones used as reactants were achieved through a rearrangement, which took place in the corresponding N-acyloxazolidinethiones.
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Physical Sciences and Engineering
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