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 |
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All Science Journal Classification (ASJC) codes
- Organic Chemistry
Cite this
The Use of Enol Trifluoromethanesulfonates as Enolate Equivalents. / Lee, Sang Ho; Hulce, Martin.
In: Synlett, Vol. 1992, No. 6, 01.06.1992, p. 485-488.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - The Use of Enol Trifluoromethanesulfonates as Enolate Equivalents
AU - Lee, Sang Ho
AU - Hulce, Martin
PY - 1992/6/1
Y1 - 1992/6/1
N2 - Enol trifluoromethanesulfonates undergo regioselective S-attack by methyllithium in diethyl ether. Resultant S-O bond cleavage cleanly generates lithium enolates.
AB - Enol trifluoromethanesulfonates undergo regioselective S-attack by methyllithium in diethyl ether. Resultant S-O bond cleavage cleanly generates lithium enolates.
UR - http://www.scopus.com/inward/record.url?scp=84992255183&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84992255183&partnerID=8YFLogxK
U2 - 10.1055/s-1992-21386
DO - 10.1055/s-1992-21386
M3 - Article
VL - 1992
SP - 485
EP - 488
JO - Synlett
JF - Synlett
SN - 0936-5214
IS - 6
ER -