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A concise stereoselective synthesis of the tetracyclic naphthoquinone (-)-isagarin

机译:简明的立体选择性合成四环萘醌(-)-isagarin

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摘要

A concise stereoselective synthesis of the tetracyclic naphthoquinone natural product (-)-isagarin has been completed in seven steps from known alkyne 5 (obtained from D-mannitol) by using D?tz benzannulation and intramolecular stereospecific dioxabicyclic ketal formation as key steps.
机译:四环萘醌天然产物(-)-isagarin的精确立体选择性合成已通过使用D?tz苯并环和分子内立体特异性二恶双环缩酮的形成,从已知炔烃5(得自D-甘露糖醇)分七个步骤完成。

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