首页> 外文期刊>Der Pharma Chemica: journal for medicinal chemistry, pharmaceutical chemistry and computational chemistry >Mild and efficient method for oxidation of alcohol to carboxylic acid followed by synthesis of amide analogues of Coreya??s lactone
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Mild and efficient method for oxidation of alcohol to carboxylic acid followed by synthesis of amide analogues of Coreya??s lactone

机译:温和有效的方法,将醇氧化为羧酸,然后合成Coreya的内酯酰胺类似物

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摘要

A mild, safe and efficient method for the oxidation of Corey’s lactone to carboxylic acid under modified Anelli’s oxidation condition has been developed. The oxidation reaction proceeded at room temperature under biphasic reaction in DCM/water with high yield. Further, treatment of carboxylic acid with various amines was studied for the first time, resulting in the formation of amides in good to excellent yields.
机译:开发了一种温和,安全,有效的方法,用于在改良的Anelli氧化条件下将Corey的内酯氧化为羧酸。氧化反应在室温下在DCM /水中的双相反应下以高收率进行。此外,首次研究了用各种胺处理羧酸的方法,从而形成了产率高至优异的酰胺。

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