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reactions with various carbon nucleo-philes to afford in highly fnctionalized 5,5-disubstitutedisoindolones, spirocyclization compound. We also foundthat β-diketone as carbon nucleophile can be used asprecursors for a π-nucleophilic attack onto allylated hydroxylactams, giving 1,2-addition products. So, allylated hydroxylactams have proven a useful

Zinc Mediated Barbier Type Allylation of Cyclic Imides and Subsequent Coupling Reactions with Carbon Nucleophiles