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Total syntheses of polyketide-derived bioactive natural products

机译:聚酮化合物衍生的生物活性天然产物的总合成

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Recent progress of total syntheses in our laboratory has been described along with our background and methodologies. The target bioactive polyketides are classified into three categories according to their structures: (i) lactone-fused polycyclic compounds [(+)-cochleamycin A, (+)tubelactomicin A, and (-)-tetrodecamycin], (ii) aromatic compounds [H-tetracycline, H-BE-54238B, lymphostin, and (-)-laguna-mycin], and (iii) acyclic polyketides [xanthocillin X dimethylether, (+)-trichostatin D, and (+)-actinopyrone A]. Features of the total syntheses are described. Original methodologies have been developed and applied to construct the inherent structures of the target molecules. Most syntheses cited herein are the first total syntheses, and the absolute structures of the target molecules have been determined. (c) 2006 The Japan Chemical Journal Forum and Wiley Periodicals, Inc.
机译:已经描述了我们实验室中总合成的最新进展以及我们的背景和方法。目标生物活性聚酮化合物根据其结构可分为三类:(i)内酯融合的多环化合物[(+)-球霉素A,(+)结核菌素A和(-)-四代卡霉素],(ii)芳香族化合物[ H-四环素,H-BE-54238B,淋巴抑制素和(-)-拉古那霉素],和(iii)无环聚酮化合物[xanthocillin X二甲醚,(+)-曲古抑菌素D和(+)-肌动吡喃酮A]。描述了总合成的特征。已经开发出原始方法并将其应用于构建靶分子的固有结构。本文引用的大多数合成是第一全部合成,并且已经确定了靶分子的绝对结构。 (c)2006年日本化学杂志论坛和Wiley期刊公司。

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