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H2O2-mediated oxidative formation of amides from aromatic amines and 1,3-diketones as acylation agents via C-C bond cleavage at room temperature in water under metal-free conditions

机译:H2O2介导的芳香族胺和1,3-二酮作为酰化剂在室温下于水中在无金属条件下通过C-C键裂解形成酰胺氧化反应

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摘要

1,3-Diketones, as novel acylation agents, reacted with aromatic amines promoted by commercially available H2O2 (30% aq.) as the sole oxidant at room temperature under metal-free conditions in water, leading to a novel and rapid amide bond formation strategy. The reported method is high-yielding, simple and mild, and is the first example of the use of 1,3-diketones as acylation agents via C-C bond cleavage.
机译:1,3-二酮作为新型的酰化剂,在室温下于水中在无金属的条件下,与市售的H2O2(30%水溶液)作为唯一的氧化剂促进的芳族胺反应,从而导致新型且快速的酰胺键形成战略。报道的方法是高产率,简单且温和的,并且是通过C-C键裂解使用1,3-二酮作为酰化剂的第一个例子。

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