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首页> 外文期刊>RSC Advances >Chan–Lam coupling reaction of sulfamoyl azides with arylboronic acids for synthesis of unsymmetrical N-arylsulfamides
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Chan–Lam coupling reaction of sulfamoyl azides with arylboronic acids for synthesis of unsymmetrical N-arylsulfamides

机译:氨磺酰基叠氮化物与芳基硼酸的Chan–Lam偶联反应用于合成不对称的N-芳基磺酰胺

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An efficient method was developed for the synthesis of unsymmetrical N -arylsulfamides using sulfamoyl azides and arylboronic acids in the presence of 10 mol% of copper chloride as the catalyst. The reaction was facilitated in MeOH in an open flask at room temperature. Unlike the coupling of sulfamides and boronic acids, the use of sulfamoyl azides was found to be beneficial with respect to the yield and reaction time.
机译:已开发出一种有效的方法,用于在氨氮为10%(摩尔)的氯化铜存在下,使用氨磺酰基叠氮化物和芳基硼​​酸合成不对称的N-芳基磺酰胺。在室温下在开放烧瓶中的MeOH中促进反应。与氨磺酰胺和硼酸的偶联不同,氨磺酰叠氮化物的使用在产率和反应时间方面是有益的。

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