Stork-Enamine Reaction || Mechanism || Acylation, Michael Addition, Enolate Chemistry | PYQ Solution

The Stork-enamine alkylation involves the nucleophilic addition of an enamine to an electrophile (alkylation reagent) or a Michael acceptor (e.g., an α,β -unsaturated carbonyl compound) to give an alkylated iminium product, which is hydrolyzed by dilute aqueous acid to give the alkylated ketone or aldehyde.
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