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Arylation with Unsymmetrical Diaryliodonium Salts: A Chemoselectivity Study

机译:非对称二芳基碘鎓盐的丙烯酸化反应:化学选择性研究

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摘要

Phenols, anilines, and malonates have been arylated under metal-free conditions with twelve aryl(phenyl)iodonium salts in a systematic chemoselectivity study. A new “anti-ortho effect” has been identified in the arylation of malonates. Several “dummy groups” have been found that give complete chemoselectivity in the transfer of the phenyl moiety, irrespective of the nucleophile. An aryl exchange in the diaryliodonium salts has been observed under certain arylation conditions. DFT calculations have been performed to investigate the reaction mechanism and to elucidate the origins of the observed selectivities. These results are expected to facilitate the design of chiral diaryliodonium salts and the development of catalytic arylation reactions that are based on these sustainable and metal-free reagents.
机译:在系统的化学选择性研究中,苯酚,苯胺和丙二酸酯已在无金属条件下与十二种芳基(苯基)碘鎓盐进行芳基化。在丙二酸酯的芳基化反应中发现了新的“反邻位效应”。已经发现了几个“虚拟基团”,它们在苯基部分的转移中具有完全的化学选择性,而与亲核试剂无关。在某些芳基化条件下已观察到二芳基碘鎓盐中的芳基交换。已进行DFT计算以研究反应机理并阐明观察到的选择性的起源。预期这些结果将促进基于这些可持续且无金属的试剂的手性二芳基碘鎓盐的设计和催化芳基化反应的发展。

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