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) |
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Pages (from-to) | 485-488 |
Number of pages | 4 |
Journal | Synlett |
Volume | 1992 |
Issue number | 6 |
DOIs | |
State | Published - Jun 1992 |
Externally published | Yes |
All Science Journal Classification (ASJC) codes
- Organic Chemistry