Abstract
Enol trifluoromethanesulfonates undergo regioselective S-attack by methyllithium in diethyl ether. Resultant S-O bond cleavage cleanly generates lithium enolates.
- Title
- The Use of Enol Trifluoromethanesulfonates as Enolate Equivalents
- Creators
- Sang Ho Lee (Author) - University of Maryland, Baltimore CountyMartin Hulce (Author) - University of Maryland, Baltimore County
- Publication Details
- Synlett, Vol.1992(6), pp.485-488
- Series
- 1992
- Number of pages
- 4
- Identifiers
- 991005929524302656
- Copyright
- : © 1992 Georg Thieme Verlag. All rights reserved.
- Academic Unit
- Creighton University
- Language
- English
- Resource Type
- Journal article