Abstract
A fast, highly efficient and green protocol for the Michael addition of active methylene compounds to styrylisoxazoles at room temperature has been investigated using task-specific basic ionic liquid, 3-butyl-1-methyl imidazolium hydroxide, [bmIm]OH, as a catalyst and green reaction medium. The reactions proceeded with excellent yields in short reaction times. The strategy is quite general and works with a variety of active methylene compounds. The ionic liquid can be recycled for subsequent reactions with consistent activity. Keyword s: Active methylene compounds, styrylisoxazole, nitroisoxazole, Michael addition, task-specific basic ionic liquid [bmIm]OH
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