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Palladium-Catalyzed Decarboxylativeortho-Acylation of Anilineswith Carbamate as a Removable Directing Group

机译:钯催化脱羧苯胺邻位酰化氨基甲酸酯作为可移动指导小组

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摘要

An efficient palladium-catalyzed decarboxylative ortho-acylation of anilines with α-oxocarboxylic acids has been realized by using carbamate as a directing group (DG). The reaction proceeds smoothly with high regioselectivity to afford diverse acylation products of aniline derivatives in moderate to good yields under mild conditions. This transformation exhibits broad substrate scope and highly functional group tolerance. In addition, the employed DG can be easily removed to give the corresponding 2-amino aromatic ketones. Importantly, several transformations of the synthesized ortho-acylated anilines into several synthetically valuable products have been demonstrated for their utilities.
机译:通过使用氨基甲酸酯作为导向基团(DG),已经实现了苯胺与α-氧代羧酸的高效钯催化的脱羧邻酰化。反应在高区域选择性的条件下平稳进行,从而在温和条件下以中等至良好的收率得到各种苯胺衍生物的酰化产物。这种转变表现出广泛的底物范围和高度官能团的耐受性。另外,可以容易地除去所用的DG,得到相应的2-氨基芳族酮。重要的是,已经证明了将合成的邻位酰化苯胺转化为几种具有合成价值的产品的实用性。

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