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Gold-catalyzed tandem reactions of amide-aldehyde-alkyne coupling and cyclization-synthesis of 2,4,5-trisubstituted oxazoles

机译:金催化的酰胺-醛-炔偶联和2,4,5-三取代恶唑环化合成的串联反应

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摘要

We report the first cationic gold(I)-catalyzed one-pot reaction of amide, alkyne and aldehyde followed by cyclization, to successfully access highly substituted oxazoles derivatives in good yields. A single catalyst allows the occurring of this multi-step reaction atom- and step-economically, with water as the only theoretical side product.
机译:我们报告了第一个阳离子金(I)催化的酰胺,炔烃和醛的单锅反应,然后进行环化反应,以高收率成功获得高度取代的恶唑衍生物。单一的催化剂可以使水作为唯一的理论副产物,以原子方式和经济方式进行多步反应。

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