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Stereoselective Total Synthesis and Structural Elucidation of (-)-Indoxamycins A-F

机译:(-)-吲哚霉素A-F的立体选择性全合成和结构解析

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摘要

In this study, a concise and stereoselective approach for the divergent total synthesis of (-)-indoxamycins A-F is described. The key steps of the strategy include an Ireland-Claisen rearrangement, an enantioselective 1,6-enyne reductive cyclization, and a tandem 1,2-addition/oxa-Michael/methylenation reaction. The relative and absolute configuration of these natural products has been unambiguously elucidated, and their cytotoxic activities against HT-29 and A-549 tumor cell lines are also reported.
机译:在这项研究中,简明和立体选择性的方法描述了(-)-茚虫霉素A-F的不同总合成。该策略的关键步骤包括爱尔兰-克莱森重排,对映选择性1,6-烯炔还原环化和串联1,2-加成/氧杂-迈克尔/甲基化反应。已经明确阐明了这些天然产物的相对和绝对构型,并且还报道了它们对HT-29和A-549肿瘤细胞系的细胞毒活性。

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