Abstract
Enol trifluoromethanesulfonates undergo regioselective S-attack by methyllithium in diethyl ether. Resultant S-O bond cleavage cleanly generates lithium enolates.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 485-488 |
| Number of pages | 4 |
| Journal | Synlett |
| Volume | 1992 |
| Issue number | 6 |
| DOIs | |
| State | Published - Jun 1 1992 |
| Externally published | Yes |
All Science Journal Classification (ASJC) codes
- Organic Chemistry
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Cite this
Lee, S. H., & Hulce, M. (1992). The Use of Enol Trifluoromethanesulfonates as Enolate Equivalents. Synlett, 1992(6), 485-488. https://doi.org/10.1055/s-1992-21386