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首页> 外文期刊>Tetrahedron >Intramolecular biaryl coupling reaction of benzyl benzoate and phenyl benzoate derivatives, and its application to the formal synthesis of (-)-steganone
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Intramolecular biaryl coupling reaction of benzyl benzoate and phenyl benzoate derivatives, and its application to the formal synthesis of (-)-steganone

机译:苯甲酸苄酯与苯甲酸苯酯衍生物的分子内联芳基偶联反应及其在(-)-steganone形式合成中的应用

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摘要

Construction of the biaryl moiety of stegane and related compounds through an intramolecular biaryl coupling reaction is described. Undesired products were obtained by the intramolecular coupling reaction of benzyl benzoates (8, 13, and 14) because of their steric and electrostatic properties, and only that of phenyl benzoates (26b and 26c) afforded the desired biaryl lactones in good yields. An asymmetric formal synthesis of the title compound has been achieved using an enantioselective lactone-opening reaction followed by a four-step conversion to the known compound. (c) 2006 Elsevier Ltd. All rights reserved.
机译:描述了通过分子内联芳基偶联反应来构造硬脂烷和相关化合物的联芳基部分。由于苯甲酸酯苄酯(8、13和14)的空间和静电性质,通过分子内偶联反应获得了不希望的产物,仅苯甲酸苯酯(26b和26c)的产物以良好的收率提供了所需的联芳基内酯。使用对映选择性内酯开放反应,然后四步转化为已知化合物,已经实现了标题化合物的不对称形式合成。 (c)2006 Elsevier Ltd.保留所有权利。

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