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首页> 外文期刊>RSC Advances >Palladium-catalyzed ligand-free and efficient Suzuki-Miyaura reaction of heteroaryl halides with MIDA boronates in water
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Palladium-catalyzed ligand-free and efficient Suzuki-Miyaura reaction of heteroaryl halides with MIDA boronates in water

机译:杂芳基卤化物与MIDA硼酸盐在水中的无钯催化高效无配体Suzuki-Miyaura反应

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摘要

A simple and environment-friendly protocol for the palladium-catalyzed ligand-free Suzuki-Miyaura reaction of heteroaryl halides with N-methyliminodiacetic acid (MIDA) boronates is developed. The reaction is performed in water as the sole medium and allows the preparation of a variety of heterobiaryls in excellent yields.
机译:开发了一种简单,环保的方案,用于杂芳基卤化物与N-甲基亚氨基二乙酸(MIDA)硼酸盐的钯催化的无配体Suzuki-Miyaura反应。该反应在作为唯一介质的水中进行,并允许以优异的产率制备各种杂联二芳基。

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