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Copper-catalyzed aerobic oxidative coupling: From ketone and diamine to pyrazine

机译:铜催化的好氧氧化偶合:从酮和二胺到吡嗪

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摘要

Copper-catalyzed aerobic oxidative C–H/N–H coupling between simple ketones and diamines was developed toward the synthesis of a variety of pyrazines. Various substituted ketones were compatible for this transformation. Preliminary mechanistic investigations indicated that radical species were involved. X-ray absorption fine structure experiments elucidated that the Cu(II) species 5 coordinated by two N atoms at a distance of 2.04 Å and two O atoms at a shorter distance of 1.98 Å was a reactive one for this aerobic oxidative coupling reaction. Density functional theory calculations suggested that the intramolecular coupling of cationic radicals was favorable in this transformation.
机译:简单的酮和二胺之间的铜催化好氧氧化C–H / N–H偶联是为合成各种吡嗪而开发的。各种取代的酮与该转化相容。初步的机械研究表明,涉及自由基。 X射线吸收精细结构实验表明,由两个N原子在2.04Å的距离和两个O原子在1.98Å的较短距离配位的Cu(II)物种5是该好氧氧化偶联反应的反应性之一。密度泛函理论计算表明,阳离子自由基的分子内偶联在该转变中是有利的。

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