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首页> 外文期刊>Organic letters >Carbocyclization of aromatic iodides, bicyclic alkenes, and benzynes involving a palladium-catalyzed C-H bond activation as a key step
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Carbocyclization of aromatic iodides, bicyclic alkenes, and benzynes involving a palladium-catalyzed C-H bond activation as a key step

机译:芳族碘化物,双环烯烃和苯炔烃的碳环化是关键步骤,涉及钯催化的C-H键活化

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摘要

A facile palladium-catalyzed carbocyclization reaction of aromatic iodides, bicyclic alkenes (norbornadiene, norbornene and oxabenzonorbornadiene), and benzynes to furnish various annulated 9,10-dihydrophenanthrene derivatives is described. The carbocyclization products from oxabenzonorbornadiene were further converted to polyaromatic hydrocarbons via a Lewis acid mediated deoxyaromatization reaction.
机译:描述了芳族碘化物,双环烯烃(降冰片二烯,降冰片烯和氧杂苯并降冰片二烯)和苯炔的钯催化碳环化反应,可提供各种环状的9,10-二氢菲衍生物。来自氧杂苯并降冰片二烯的碳环化产物通过路易斯酸介导的脱氧芳构化反应进一步转化为多芳烃。

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