首页> 外文期刊>The Journal of Organic Chemistry >Synthesis of Chromones via Palladium-Catalyzed Ligand-Free Cyclocarbonylation of o-lodophenols with Terminal Acetylenes in Phosphonium Salt Ionic Liquids
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Synthesis of Chromones via Palladium-Catalyzed Ligand-Free Cyclocarbonylation of o-lodophenols with Terminal Acetylenes in Phosphonium Salt Ionic Liquids

机译:在Pal盐离子液体中通过钯催化邻位苯酚与末端乙炔的邻位苯酚的无配体环羰基化反应合成色酮

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摘要

The highly efficient and selective palladium-catalyzed ligand-free cyclocarbonylation reaction of o-iodophenols with terminal acetylenes and CO in the phosphonium salt ionic liquid, C141-129(C6I113)3F+ Br-, affords diversified chromones in good to excellent yields under atmospheric CO pressure. The ionic liquid, as the reaction medium, enhances the efficiency of the cyclocarbonylation reaction.
机译:141盐离子液体C141-129(C6I113)3F + Br-中的邻位碘苯酚与末端乙炔和CO的高效,选择性钯催化的无配体无配体环羰基化反应,在常压CO下可提供良好至优异收率的多种色酮压力。离子液体作为反应介质,提高了环羰基化反应的效率。

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