γ-Substituted butyrolactones from acrolein and carbonyl compounds
Abstract
The lithiation of 3-chloropropanal diethyl acetal (easily prepared from acrolein) at –78 °C with lithium naphthalenide followed by reaction with various carbonyl compounds, and final oxidation with m-chloroperbenzoic acid leads to γ-substituted butyrolactones.
 
                



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