| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 7752874 | Journal of Fluorine Chemistry | 2015 | 26 Pages |
Abstract
- The reactivity of (E)-4,4,4-trifluorobut-2-en-1-yl 4-methylbenzenesulfonate towards different nucleophiles was performed.
- Phenol, amines, thiols, and malonates all provide the substitution product in moderate to excellent yields.
- Benzyl alcohol and indole provide low yield of the desired product.
Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
Elsa Forcellini, Rémy Hemelaere, Justine Desroches, Jean-François Paquin,