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Acylation des β-énaminoesters: Regio et stéréoformation des β-énaminoesters N- ou C-acylés
Authors:Pascal Brunerie  Jean-Pierre Clrier  Huguette Petit  Grard Lhommet
Institution:Pascal Brunerie,Jean-Pierre Célérier,Huguette Petit,Gérard Lhommet
Abstract:The reaction of acyl chlorides with cyclic five-membered β-enaminoesters gave exclusively N-acylated products while reaction of acyl chlorides with cyclic seven-membered β-enaminoesters gave only C-acylated products. In the case of cyclic six-membered β-enaminoesters, the reaction of acyl chlorides gave a mixture of N-acylated and C-acylated products.
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