首页> 外文期刊>The Journal of Organic Chemistry >Synthesis of the Tetracyclic Cores of the Integrastatins, Epicoccolide A and Epicocconigrone A
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Synthesis of the Tetracyclic Cores of the Integrastatins, Epicoccolide A and Epicocconigrone A

机译:整体蛋白的四环芯,摘要A和Epicoconigrone的合成

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摘要

The integrastatins, epicoccolide A and epicoccongirone A, are natural products containing a unique [6.6.6.6]-tetracyclic core framework that exhibit a broad spectrum of biological activities. A synthesis of the common core of epicoccolide A and epicocconigrone A has been achieved using an umpolung alkylation-lactonization to assemble an isochromanone from which the bridged 1,3-dioxane was readily assembled. A different strategy was required to access the core on the integrastatins; an initial aryllithium addition to an aldehyde, followed by oxidation and treatment of the masked dihydroxyketone with acid gave the desired core structure.
机译:瘦蛋白质,表皮灰醇A和Epicoccongerone A,是含有独特的[6.6.6.6]的天然产物,其具有广泛的生物活性谱。 使用umpolung烷基化 - 内酰胺化进行了胶质晶体A和表情胶质通孔A的共同核的合成,以组装桥接1,3-二恶烷的等色素。 进入亚体塑壳上的核心需要不同的策略; 醛的初始芳基锂除了氧化和处理掩蔽二羟基酮与酸的氧化铝基锂,得到了所需的核心结构。

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