Synthesis of xestobergsterol A from dehydroepiandrosterone
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摘要
Xestobergsterol A, a potent inhibitor of histamine release, has been synthesized from dehydroepiandrosterone in a route that used introduction of a novel 15-oxygen functionality, side-chain construction via the orthoester Claisen rearrangement and TBAF-promoted epimerization–aldol condensation.

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