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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/2929
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dc.contributor.authorKumar, Anil-
dc.date.accessioned2021-10-27T04:10:19Z-
dc.date.available2021-10-27T04:10:19Z-
dc.date.issued2011-10-12-
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0040403911013323?via%3Dihub-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2929-
dc.description.abstractA novel task-specific ionic liquid, 1-butyl-3-methylimidazolium p-toluenesulfinate, [bmim][p-TolSO2] has been synthesized and used as a nucleophile for the reaction with alkyl bromides and phenacyl bromides to prepare sulfones and β-ketosulfones in excellent yields (80–93%) in [bmim][BF4] ionic liquid. The isolated yields of sulfones and β-ketosulfones were higher in [bmim][BF4] than other organic solvents at room temperature.en_US
dc.language.isoenen_US
dc.publisherElsieveren_US
dc.subjectChemistryen_US
dc.subjectIonic liquiden_US
dc.subjectTask-specific ionic liquiden_US
dc.subjectβ-Ketosulfonesen_US
dc.subjectNucleophilic substitutionen_US
dc.subjectPhenacyl bromidesen_US
dc.title1-Butyl-3-methylimidazolium p-toluenesulfinate: a novel reagent for synthesis of sulfones and β-ketosulfones in ionic liquiden_US
dc.typeArticleen_US
Appears in Collections:Department of Chemistry

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