Abstract
Cerium(IV) ammonium nitrate-mediated oxidative radical reactions are carried out in the presence of ionic liquids, including 1-butyl-3-methylimidazolium tetrafluoroborate, for the first time. The presence of the ionic liquid not only increases the rate and yield of reactions in dichloromethane but also extends the range of 1,3-dicarbonyl precursors, which can be utilized in these carbon-carbon bond-forming reactions.
Original language | English |
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Pages (from-to) | 213-222 |
Number of pages | 10 |
Journal | SYNTHETIC COMMUNICATIONS |
Volume | 33 |
Issue number | 2 |
DOIs | |
Publication status | Published - 2003 |
Keywords
- radical reactions
- ionic liquids
- CERIUM(IV) AMMONIUM-NITRATE
- MANGANESE(III) ACETATE
- 1,3-DICARBONYL COMPOUNDS
- QUINOLINE ALKALOIDS
- EFFICIENT SYNTHESIS
- ALKENES
- CYCLIZATION
- DIHYDROFUROQUINOLINONES
- FUROQUINOLINONES
- CYCLOADDITION