Acylation des β-énaminoesters: Regio et stéréoformation des β-énaminoesters N- ou C-acylés |
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Authors: | Pascal Brunerie Jean-Pierre Clrier Huguette Petit Grard Lhommet |
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Institution: | Pascal Brunerie,Jean-Pierre Célérier,Huguette Petit,Gérard Lhommet |
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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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