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Trimethylsilylethynyl ketones as surrogates for ethynyl ketones in the double Michael reaction
Authors:Holeman Derrick S  Rasne Ravindra M  Grossman Robert B
Institution:Department of Chemistry, University of Kentucky, Lexington, Kentucky 40506-0055, USA.
Abstract:Trimethylsilylethynyl ketones can be desilylated in the presence of a tethered carbon diacid and induced to undergo a double Michael reaction in situ. The trimethylsilylethynyl ketones can serve as surrogates of ethynyl ketones that are difficult to prepare or isolate.
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