An imidazolinium salt as ionic liquid for medium and strong bases
- 13 October 2005
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Green Chemistry
- Vol. 7 (12), 844-848
- https://doi.org/10.1039/b511062a
Abstract
An imidazolinium salt incorporating a phenyl ring at the C-2 position has been found to be an ionic liquid suitable as a solvent for reactions involving medium and strong bases like quinuclidine and Grignard reagents.Keywords
This publication has 25 references indexed in Scilit:
- Low-melting sugar–urea–salt mixtures as solvents for Diels–Alder reactionsChemical Communications, 2005
- Phosphonium ionic liquids as reaction media for strong basesChemical Communications, 2005
- Imidazolinium salts as catalysts for the aza-Diels–Alder reactionOrganic & Biomolecular Chemistry, 2004
- On the Noninnocent Nature of 1,3‐Dialkylimidazolium Ionic LiquidsAngewandte Chemie-International Edition, 2004
- Aromatic nitrations in ionic liquids: the importance of cation choiceChemical Communications, 2003
- Steric Factors Direct Baylis−Hillman and Aldol Reactions in Titanium Tetrachloride Mediated Coupling between α-Keto Esters and Cyclohex-2-enone DerivativesThe Journal of Organic Chemistry, 2003
- In Situ Formation of Mixed Phosphine−Imidazolylidene Palladium Complexes in Room-Temperature Ionic LiquidsOrganometallics, 2001
- Stereoselective generation and facile dimerization of (E)-2-methylene-3-alkenoic acid estersThe Journal of Organic Chemistry, 1988
- Acid-catalyzed ring-chain tautomerism in 1,3-diazolidinesThe Journal of Organic Chemistry, 1987
- LIX.—The action of aldehydes on the Grignard reagent. Part IIJournal of the Chemical Society, Transactions, 1915