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A metal-free and mild approach to 1,3,4- oxadiazol-2(3H)-ones via oxidative C-C bond cleavage using molecular oxygen

机译:使用分子氧通过氧化性C-C键裂解,实现无金属,温和的1,3,4-恶二唑-2(3H)-酮的合成方法

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摘要

A mild metal-free approach to l,3,4-oxadiazol-2(3H)-ones via 1,3,4-oxadiazin-5(6H)-ones is described. This novel transformation, promoted by the electron-withdrawing p-substituents on the phenyl group at the α-carbonyl position, features a tandem reaction consisting of oxidative hydroxylation and C-C bond cleavage using molecular oxygen. The method utilizes K_2CO_3 in CH_3CN without any oxidants, transition metals, or additives, enabling the tunable synthesis of 1,3,4-oxadiazin-5(6H)-ones, 1,3,4-oxadiazol-2(3H)-ones, and α-ketoamides under mild aerobic conditions.
机译:描述了经由1,3,4-恶二嗪-5(6H)-酮的1,3,4-恶二唑-2(3H)-酮的温和无金属方法。由α-羰基位置上的苯基上的吸电子p-取代基促进的这种新的转变具有串联反应,该串联反应由氧化羟基化和使用分子氧进行的C-C键裂解组成。该方法利用CH_3CN中的K_2CO_3而没有任何氧化剂,过渡金属或添加剂,从而可调谐合成1,3,4-恶二嗪-5(6H)-one,1,3,4-恶二唑-2(3H)-one。和α-酮酰胺在温和的有氧条件下。

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  • 来源
    《Organic & biomolecular chemistry》 |2018年第12期|2105-2113|共9页
  • 作者单位

    College of Pharmacy, Research Institute of Pharmaceutical sciences, Seoul National University, 1 Gwanak-ro, Gwa-nak-gu, Seoul 08826, Korea;

    College of Pharmacy, Research Institute of Pharmaceutical sciences, Seoul National University, 1 Gwanak-ro, Gwa-nak-gu, Seoul 08826, Korea;

    College of Pharmacy, Research Institute of Pharmaceutical sciences, Seoul National University, 1 Gwanak-ro, Gwa-nak-gu, Seoul 08826, Korea;

    Department of Medicinal Bioscience, College of Interdisciplinary & Creative Studies, Konyang University, 121 Daehak-ro, Nonsan, Chungnam, Korea;

    College of Pharmacy, Research Institute of Pharmaceutical sciences, Seoul National University, 1 Gwanak-ro, Gwa-nak-gu, Seoul 08826, Korea;

    Department of Energy Science, Sungkyunkwan University, Suwon 16419, South Korea;

    College of Pharmacy, Research Institute of Pharmaceutical sciences, Seoul National University, 1 Gwanak-ro, Gwa-nak-gu, Seoul 08826, Korea;

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