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Co-complexes Derived from Alkene Insertion to Alkyne-dicobaltpentacarbonyl complexes: Insight into the Regioselectivity of Pauson-Khand Reactions of Cyclopropenes

机译:从烯烃插入到炔-二钴五羰基配合物的共配合物:环丙烯的Pauson-Khand反应的区域选择性的见解

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摘要

Described are the X-ray crystallographic and spectral properties of Co-complexes that were isolated from two Pauson-Khand reactions of chiral cyclopropenes. These are the first examples of isolated Co-complexes derived from the putative alkene-insertion intermediates of Pauson-Khand reactions. The binuclear Co-complexes are coordinated to μ-bonded, five-carbon “flyover” carbene ligands. It is proposed that the complexes result from cyclopropane fragmentation subsequent to alkene insertion. The observation of these metal complexes provides a rationale for the origin of regioselectivity in Pauson-Khand reactions of cyclopropenes.
机译:描述了从两个手性环丙烯的Pauson-Khand反应中分离出的Co-配合物的X射线晶体学和光谱性质。这些是衍生自Pauson-Khand反应的假定的烯烃插入中间体的分离的Co-配合物的第一个实例。双核共配合物与μ键合的五碳“跨线”卡宾配体配位。提出该络合物是由烯烃插入后的环丙烷裂解产生的。这些金属配合物的观察为环丙烯的Pauson-Khand反应中区域选择性的起源提供了理论依据。

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