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首页> 外文期刊>Synthesis: International Journal of Methods in Synthetic Organic Chemistry >Synthesis of selectively substituted ortho-vinylbiphenyls by palladium-catalysed reaction of ortho-substituted aryl iodides with olefins
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Synthesis of selectively substituted ortho-vinylbiphenyls by palladium-catalysed reaction of ortho-substituted aryl iodides with olefins

机译:通过钯催化的邻位取代的芳基碘化物与烯烃的反应合成选择性取代的邻位乙烯基联苯

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摘要

In the presence of Pd(OAc)(2) and norbornene as catalysts, ortho-substituted aryl iodides and terminal olefins react to afford selectively substituted ortho-vinylbiphenyl derivatives in good yields. The reaction proceeds through a series of steps including norbornene insertion and C-H activation with formation of palladacycles able to promote arylation of their aromatic part. Norbornene deinsertion then leads to the selective formation of a palladium-bonded biphenylyl group able to react with terminal olefins. [References: 46]
机译:在Pd(OAc)(2)和降冰片烯作为催化剂的存在下,邻位取代的芳基碘化物和末端烯烃发生反应,以高收率提供了选择性取代的邻位乙烯基联苯衍生物。该反应通过一系列步骤进行,包括降冰片烯插入和C-H活化以及形成能够促进其芳族部分芳基化的Palladacycles。然后降冰片烯的去插入导致能够与末端烯烃反应的钯键合联苯苯基的选择性形成。 [参考:46]

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