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首页> 外文期刊>Organic & biomolecular chemistry >Metal-free enantioselective addition of nucleophilic silicon to aromatic aldehydes catalyzed by a [2.2]paracyclophane-based N-heterocyclic carbene catalyst
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Metal-free enantioselective addition of nucleophilic silicon to aromatic aldehydes catalyzed by a [2.2]paracyclophane-based N-heterocyclic carbene catalyst

机译:[2.2]基于对环环烷的N-杂环卡宾催化剂催化的无金属对苯二酚对苯二酚的对映选择性

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摘要

The first example of transition metal-free enantioselective 1,2-sily-lation of aromatic aldehydes is reported. This protocol enables an easy access to chiral α-hydroxysilanes from readily available aromatic aldehydes.
机译:报道了芳族醛的无过渡金属的对映选择性1,2-甲硅烷基化的第一个例子。该方案使得容易从容易获得的芳族醛中获得手性α-羟基硅烷。

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  • 来源
    《Organic & biomolecular chemistry》 |2017年第15期|3202-3206|共5页
  • 作者单位

    School of Pharmaceutical Sciences, Shandong University, West Wenhua Road No. 44, Jinan 250012, P. R. China;

    Department of Chemistry, Shandong University, Shanda South Road No. 27, Jinan 250100, P. R. China;

    School of Chemistry and Chemical Engineering, Hebei Normal University For Nationalities, Higher Education Park, Chengde 0670000, P. R. China;

    School of Pharmaceutical Sciences, Shandong University, West Wenhua Road No. 44, Jinan 250012, P. R. China;

    Department of Chemistry, Shandong University, Shanda South Road No. 27, Jinan 250100, P. R. China;

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