Treatment of N-allylamides 1a–c and lactams 1d–f with molecular oxygen in the presence of [PdCl2(MeCN)2]–CuCl catalyst in anhydrous 1,2-dichloroethane containing hexamethylphosphoric triamide gives the corresponding aldehydes 2 regioselectively, while methyl ketones 3 become the major products in the presence of water.
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Hosokawa et al. (1991) studied this question.
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