首页> 外文期刊>Organic letters >Nickel(0)/N-Heterocyclic Carbene-Catalyzed Asymmetric [2+2+2] Cycloaddition of Two Enones and an Alkyne: Access to Cyclohexenes with Four Contiguous Stereogenic Centers
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Nickel(0)/N-Heterocyclic Carbene-Catalyzed Asymmetric [2+2+2] Cycloaddition of Two Enones and an Alkyne: Access to Cyclohexenes with Four Contiguous Stereogenic Centers

机译:镍(0)/ N-杂环碳烯催化的两个烯酮和炔烃的不对称[2 + 2 + 2]环加成反应:获得具有四个连续立体中心的环己烯

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摘要

A nickel(0)/chiral N-heterocyclic carbene (NHC)-catalyzed fully intermolecular, enantioselective [2 + 2 + 2] cycloaddition of two enones and an alkyne has been developed to access enantioenriched cyclohexenes. A single diastereomer was obtained with a successive generation of four contiguous stereogenic centers. The absolute configuration of cyclohexene derivative 3aa was determined by X-ray diffraction and circular dichroism (CD) spectral studies.
机译:镍(0)/手性N-杂环卡宾(NHC)催化的两个烯酮的全分子间,对映选择性[2 + 2 + 2]环加成反应和炔烃已开发出来,可用于访问富含对映体的环己烯。获得了一个非对映异构体,连续生成了四个连续的立体异构中心。通过X射线衍射和圆二色性(CD)光谱研究确定了环己烯衍生物3aa的绝对构型。

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