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http://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/2929Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Kumar, Anil | - |
| dc.date.accessioned | 2021-10-27T04:10:19Z | - |
| dc.date.available | 2021-10-27T04:10:19Z | - |
| dc.date.issued | 2011-10-12 | - |
| dc.identifier.uri | https://www.sciencedirect.com/science/article/pii/S0040403911013323?via%3Dihub | - |
| dc.identifier.uri | http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2929 | - |
| dc.description.abstract | A 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.iso | en | en_US |
| dc.publisher | Elsiever | en_US |
| dc.subject | Chemistry | en_US |
| dc.subject | Ionic liquid | en_US |
| dc.subject | Task-specific ionic liquid | en_US |
| dc.subject | β-Ketosulfones | en_US |
| dc.subject | Nucleophilic substitution | en_US |
| dc.subject | Phenacyl bromides | en_US |
| dc.title | 1-Butyl-3-methylimidazolium p-toluenesulfinate: a novel reagent for synthesis of sulfones and β-ketosulfones in ionic liquid | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | Department of Chemistry | |
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