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A short and efficient total synthesis of the bromotyrosine-derived alkaloid psammaplysene A

机译:溴酪氨酸衍生的生物碱苯丙氨酸A的短而有效的全合成

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摘要

Psammaplysene A, an inhibitor of FOXO1a-mediated nuclear export, has been synthesized by a concise and improved route from tyrosine-derived acid and amine fragments which were easily constructed using commercially available p -hydroxybenzaldehyde and tyramine as starting material, respectively. The strategy provides an efficient access of psammaplysene analogues that can be explored for potential pharmaceutical or biological activities.
机译:通过简化和改进的途径,由酪氨酸衍生的酸和胺片段合成了FOXO1a介导的核出口抑制剂,即邻苯二甲酚A,它们分别使用可商购的对羟基苯甲醛和酪胺作为起始原料容易地构建。该策略提供了可用于潜在的药物或生物活性的对苯二酚类似物的有效利用。

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