Design of Reaction Media for Nucleophilic Substitution Reactions by Using a Catalytic Amount of an Amphiphilic Imidazolium Salt in Water
- 1 January 2010
- journal article
- Published by The Japan Institute of Heterocyclic Chemistry in HETEROCYCLES
- Vol. 80 (2), 989
- https://doi.org/10.3987/com-09-s(s)71
Abstract
No abstract availableKeywords
This publication has 42 references indexed in Scilit:
- Amphiphilic Organocatalyst for Schotten-Baumann-Type Tosylation of Alcohols under Organic Solvent Free ConditionOrganic Letters, 2009
- N-Alkylimidazole as Amphiphilic Organocatalyst: ‘Catalytic’ Morita-Baylis-Hillman Reaction on Water without Organic SolventSynlett, 2008
- Micelle formation of imidazolium ionic liquids in aqueous solutionColloids and Surfaces A: Physicochemical and Engineering Aspects, 2008
- Micelle formation of 1-alkyl-3-methylimidazolium bromide ionic liquids in aqueous solutionColloids and Surfaces A: Physicochemical and Engineering Aspects, 2007
- Significantly Enhanced Reactivities of the Nucleophilic Substitution Reactions in Ionic LiquidThe Journal of Organic Chemistry, 2003
- Ionic liquids in regioselective platinum-catalysed hydroformylationJournal of Molecular Catalysis A: Chemical, 2000
- Water-Promoted Organic ReactionsSynthesis, 1994
- Aqueous intermolecular Diels-Alder chemistry: reactions of diene carboxylates with dienophiles in water at ambient temperatureThe Journal of Organic Chemistry, 1983
- Hydrophobic acceleration of Diels-Alder reactionsJournal of the American Chemical Society, 1980
- Catalysis in molten salt mediaJournal of the American Chemical Society, 1972