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首页> 外文期刊>Organic letters >Selective Rhenium-Catalyzed Oxidation of Secondary Alcohols with Methyl Sulfoxide in the Presence of Ethylene Glycol, a Convenient One-Pot Synthesis of Ketals
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Selective Rhenium-Catalyzed Oxidation of Secondary Alcohols with Methyl Sulfoxide in the Presence of Ethylene Glycol, a Convenient One-Pot Synthesis of Ketals

机译:在乙二醇存在下便捷地一锅合成缩酮的选择性hen催化仲醇与甲基亚砜的氧化

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摘要

Secondary alcohols are oxidized preferentially by DMSO and the catalyst ReOCl_3(PPh_3)_2 in the presence of ethylene glycol and refluxing toluene, producing the corresponding ketals. The reactions are rapid, and proceed in very good to excellent yields. The byproducts of the reaction, methyl sulfide and water, are easily removed. No epoxidation or other common side reactions were observed. This direct oxidative transformation of alcohols to the protected ketal derivatives should have broad synthetic applicability.
机译:在乙二醇和回流的甲苯存在下,仲醇优先被DMSO和催化剂ReOC1-3(PPh_3)_2氧化,生成相应的缩酮。反应是快速的,并且以非常好的产率进行。反应的副产物甲基硫化物和水很容易除去。没有观察到环氧化或其他常见的副反应。醇向被保护的缩酮衍生物的这种直接氧化转化应具有广泛的合成适用性。

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