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Preparation of adamantyl derivatives of 1,4-; 1,6- and 1,7- dihydroxynaphthalenes and assignment of their NMR data

机译:1,4-金刚烷衍生物的制备; 1,6-和1,7-二羟基萘及其NMR数据分配

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Adamantylation of dihydroxynaphthalenes with the hydroxyl groups on the same or different rings leads to compounds that are convenient starting materials in target-oriented organic synthesis. Here, we report the ~1H and ~(13)C NMR assignments of eight 1-adamantyl substituted derivatives of 1,4-; 1,6- and 1,7-dihydroxynaphthalenes. The data acquired and peculiarities of their molecular structure are useful for extrapolation for prompt characterization of compounds containing adamantane, dihydroxynaphthalenes or naphthoquinone units. Copyright ? 2013 John Wiley & Sons, Ltd. Adamantylation of dihydroxynaphthalenes with the hydroxyl groups on the same or different rings leads to compounds that are convenient starting materials in target-oriented organic synthesis. The synthesis of eight 1-adamantyl substituent derivatives of 1,4-; 1,6- and 1,7-dihydroxynaphthalenes and assignments of ~1H and ~(13)C NMR spectra are described.
机译:在相同或不同环上带有羟基的二羟基萘的金刚烷基化反应会生成化合物,这些化合物是目标定向有机合成中方便的起始原料。在这里,我们报告了8个1,4-的1-金刚烷基取代的衍生物的〜1H和〜(13)C NMR分配; 1,6-和1,7-二羟基萘。所获得的数据及其分子结构的特点可用于外推,以快速表征含有金刚烷,二羟基萘或萘醌单元的化合物。版权? 2013 John Wiley&Sons,Ltd.在相同或不同环上带有羟基的二羟基萘的金刚烷基化反应会生成化合物,该化合物可作为目标定向有机合成的便捷起始原料。八个1,4-金刚烷基取代基衍生物的合成描述了1,6-和1,7-二羟基萘以及〜1H和〜(13)C NMR光谱的归属。

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