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首页> 外文期刊>Angewandte Chemie >Palladium-Catalyzed Direct Dialkenylation of Cage BH Bonds in o-Carboranes through Cross-Coupling Reactions
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Palladium-Catalyzed Direct Dialkenylation of Cage BH Bonds in o-Carboranes through Cross-Coupling Reactions

机译:通过交叉偶联反应,钯催化邻位碳硼烷中笼型BH键的直接二烯基化

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摘要

Palladium-catalyzed direct dialkenylation of cage B(4,5)H bonds in o-carboranes has been achieved with the help of a carboxylic acid directing group, leading to the preparation of a series of 4,5-[trans-(ArCHCH)](2)-ocarboranes in high yields with excellent regioselectivity. The traceless directing group, eliminated during the course of the reaction, is responsible for controlling regioselectivity and dialkenylation. A possible catalytic cycle is proposed, involving a tandem sequence of Pd-II-initiated cage BH activation, alkene insertion, -H elimination, reductive elimination, and decarboxylation.
机译:借助于羧酸导向基团,已实现了邻氨基甲酸酯中钯催化的笼状B(4,5)H键的直接二烯基化,从而制备了一系列4,5- [反式-(ArCHCH)高产率的](2)-碳碳烷酮,具有出色的区域选择性。在反应过程中消除的无痕导向基团负责控制区域选择性和二烯基化。提出了可能的催化循环,涉及Pd-II引发的笼状BH活化,烯烃插入,-H消除,还原消除和脱羧的串联序列。

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