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首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >A one-pot synthesis of 3-substituted-5-carbonylmethyl-1,2,4-oxadiazoles from beta-keto esters and amidoximes under solvent-free conditions
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A one-pot synthesis of 3-substituted-5-carbonylmethyl-1,2,4-oxadiazoles from beta-keto esters and amidoximes under solvent-free conditions

机译:在无溶剂条件下由β-酮酯和a肟一锅法合成3-取代的5-羰基甲基-1,2,4-恶二唑

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摘要

Herein we report a high yielding one-pot 'green' synthesis of 3-substituted-5-carbonylmethyl-l,2,4-oxadiazoles from readily available beta-keto esters and amidoximes under simple and convenient solvent-free conditions.No additional base is needed.The reaction likely goes through an acyl ketene intermediate.
机译:本文中我们报道了在简单,方便的无溶剂条件下,从容易获得的β-酮酯和a胺肟中高产率地一锅式``绿色''合成3-取代的5-羰基甲基-1,2,4-恶二唑的过程。该反应可能会通过酰基乙烯酮中间体进行。

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