| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5219976 | Tetrahedron | 2011 | 5 Pages |
Abstract
A simple and efficient Et3N-mediated transesterification between β-keto esters and Baylis-Hillman alcohols in toluene solution at reflux using a Dean-Stark apparatus, is described. Allylic esters are exclusively obtained in moderate to good yields, with no trace amounts of γ,δ-unsaturated ketones usually expected from the Carroll decarboxylative rearrangement.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Olfa Mhasni, Farhat Rezgui,