Abstract
Abstract Lithium diisopropylamide, reacts with trifluoromethylketones either as a base in polar solvents or as a hydride donor in hexane. In the presence of tert -Butyldimethylsilyl chloride, Lithium diisopropylamide allows the transformation of trifluoromethylketones into silyl enol ethers or silyl carbinols using an appropriate solvent.
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