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The Total Synthesis of (−)-Scabrolide A

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NIAID Data Ecosystem2026-03-11 收录
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https://figshare.com/articles/dataset/The_Total_Synthesis_of_-Scabrolide_A/12221291
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The first total synthesis of the norcembranoid diterpenoid scabrolide A is disclosed. The route begins with the synthesis of two chiral pool-derived fragments, which undergo a convergent coupling to expediently introduce all 19 carbon atoms of the natural product. An intramolecular Diels–Alder reaction and an enone–olefin cycloaddition/fragmentation sequence are then employed to construct the fused [5–6–7] linear carbocyclic core of the molecule and complete the total synthesis.
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2020-03-30
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