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Cited by 513

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Diels–Alder reactions in ionic liquids

Earle, Martyn J., McCormac, Paul B., Seddon, Kenneth R.·1999·Green Chemistry
DOI 10.1039/a808052f
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Abstract

Diels–Alder reactions in neutral ionic liquids (such as 1-butyl-3-methylimidazolium trifluoromethanesulfonate, 1-butyl-3-methylimidazolium hexafluorophosphate, 1-butyl-3-methylimidazolium tetrafluoroborate, and 1-butyl-3-methyl-imidazolium lactate) are reported. Rate enhancements and selectivities similar to those of reactions performed in lithium perchlorate–diethyl ether mixtures have been observed. As the ionic liquids used have no measurable vapour pressure, are thermally robust, will tolerate impurities such as water, and are recyclable, it is envisaged that these systems could be used on an industrial scale.

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Metadata

Authors
Earle, M. J., McCormac, P. B., & Seddon, K. R.
Venue
Green Chemistry
Publisher
Royal Society of Chemistry (RSC)
Published
1999
Volume
1
Issue
1
Pages
23-25
ISSN
  • 1463-9262 (ISSN-L)
  • 1463-9270
DOI
10.1039/a808052f
OpenAlex
W1922431434
Cited by
513
References
0
FWCI
9.91
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Diels–Alder reactions in ionic liquids. https://app.cochat.ai/papers/10.1039/a808052f
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Earle, M. J., McCormac, P. B., & Seddon, K. R. (1999). Diels–Alder reactions in ionic liquids. Green Chemistry. https://doi.org/10.1039/a808052f

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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