The Use of Enol Trifluoromethanesulfonates as Enolate Equivalents

Sang Ho Lee; Martin Hulce

doi:10.1055/s-1992-21386

The Use of Enol Trifluoromethanesulfonates as Enolate Equivalents

Sang Ho Lee, Martin Hulce

Research output: Contribution to journal › Article › peer-review

7 Scopus citations

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	https://doi.org/10.1055/s-1992-21386
State	Published - Jun 1992
Externally published	Yes

All Science Journal Classification (ASJC) codes

Organic Chemistry

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title = "The Use of Enol Trifluoromethanesulfonates as Enolate Equivalents",

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

author = "Lee, {Sang Ho} and Martin Hulce",

year = "1992",

month = jun,

doi = "10.1055/s-1992-21386",

language = "English (US)",

volume = "1992",

pages = "485--488",

journal = "Synlett",

issn = "0936-5214",

publisher = "Georg Thieme Verlag",

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AU - Lee, Sang Ho

AU - Hulce, Martin

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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.

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U2 - 10.1055/s-1992-21386

DO - 10.1055/s-1992-21386

M3 - Article

AN - SCOPUS:84992255183

VL - 1992

SP - 485

EP - 488

JO - Synlett

JF - Synlett

SN - 0936-5214

IS - 6

ER -

The Use of Enol Trifluoromethanesulfonates as Enolate Equivalents

Abstract

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