Protecting-Group-Free Total Synthesis of Aplykurodinone-1
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文摘
A concise, stereoselective, and protecting-group-free total synthesis of aplykurodinone-1 from Hajos鈥揚arrish ketone was described. The synthetic approach features a sequence of aerobic allylic oxidation and elimination of alcohol 9. The key intermediate for this synthesis was formed by a stereoselective intramolecular radical cyclization.

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