The Use of Enol Trifluoromethanesulfonates as Enolate Equivalents

Sang Ho Lee, Martin Hulce

Research output: Contribution to journalArticle

7 Citations (Scopus)

Abstract

Enol trifluoromethanesulfonates undergo regioselective S-attack by methyllithium in diethyl ether. Resultant S-O bond cleavage cleanly generates lithium enolates.

Original languageEnglish (US)
Pages (from-to)485-488
Number of pages4
JournalSynlett
Volume1992
Issue number6
DOIs
StatePublished - Jun 1 1992
Externally publishedYes

Fingerprint

Lithium
Ether
methyllithium
trifluoromethanesulfonic acid

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 journalArticle

Lee, Sang Ho ; Hulce, Martin. / The Use of Enol Trifluoromethanesulfonates as Enolate Equivalents. In: Synlett. 1992 ; Vol. 1992, No. 6. pp. 485-488.
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