| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5268836 | Tetrahedron Letters | 2010 | 4 Pages |
Abstract
KF-alumina was found to be an efficient base for the synthesis of sterically hindered α-substituted carboxylic acids. A series of Bargellini reactions were performed by using various substituted anilines, phenols, and thiophenols as nucleophiles with ketones in the presence of chloroform and KF-alumina as a base. All the compounds were fully characterized.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Md. Rumum Rohman, Bekington Myrboh,