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Synthesis of Rocaglamide Natural Products Via Photochemical Generation of Oxidopyrylium Species

机译:通过光化学产生氧化吡啶鎓物种合成Rocaglamide天然产物

摘要

The present invention provides new strategies for the synthesis of compounds of the rocaglamide family and related natural products. In particular, the new biomimetic synthetic approach involves photochemical generation of an oxidopyrylium species from a 3-hydroxychromone derivative followed by 1,3-dipolar cycloaddition of the oxidopyrylium species to a dipolarophile. This approach can be used for the formation of adducts containing an aglain core structure. Methods for the conversion of aglain core structures to aglain, rocaglamide and forbaglin ring systems are also provided. The present invention also relates to the use of rocaglamide/aglain/forbaglin derivatives for the manufacture of medicaments for use in the treatment of cancer or cancerous conditions, disorders associated with cellular hyperproliferation, or NF-κB-dependent conditions.
机译:本发明提供了罗格列酰胺家族化合物和相关天然产物的合成的新策略。特别地,新的仿生合成方法涉及从3-羟基色酮衍生物光化学生成氧化吡咯类物质,然后将氧化吡咯类物质进行1,3-偶极环加成成双极性亲核体。该方法可用于形成包含琼脂糖蛋白核心结构的加合物。还提供了将琼脂素核心结构转化为琼脂素,罗格列酰胺和forbag​​lin环系统的方法。本发明还涉及罗格列酰胺/琼脂糖蛋白/福尔巴林衍生物在制备用于治疗癌症或癌性疾病,与细胞过度增殖相关的疾病或NF-κB依赖性疾病的药物中的用途。

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