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Exploration of 1,2-phenylenediboronic esters as potential bidentate catalysts for organic synthesis

机译:1,2-苯二硼酸酯作为有机合成潜在的双齿催化剂的探索

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摘要

Recently, we described the first inverse electron demand Diels-Alder reaction of 1,2-diazene catalyzed by a bidentate Lewis acid. Herein we investigate 1,2-phenylenediboronic esters as potential catalysts for this transformation offering higher stability and easier handling than the currently used boranthracene derivatives. Different 1,2-phenylenediboronic esters were prepared and their ability to form bidentate coordination complexes with phthalazine was analyzed. Although a 1:1 complex was observed, X-ray analysis revealed binding only in a monodentate fashion.
机译:最近,我们描述了由双齿路易斯酸催化的1,2-二氮烯的第一个逆电子需量Diels-Alder反应。在本文中,我们研究了1,2-苯二硼酸酯作为该转化的潜在催化剂,与目前使用的硼蒽衍生物相比,具有更高的稳定性和更易于操作。制备了不同的1,2-苯二酸硼酸酯,并分析了它们与邻苯二甲酰胺形成二齿配位络合物的能力。尽管观察到1:1的复合物,但是X射线分析显示仅以单齿方式结合。

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