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Asymmetric Total Synthesis of (−)-Vinigrol

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NIAID Data Ecosystem2026-03-11 收录
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A new strategy was developed for the asymmetric total synthesis of (−)-vinigrol. The strategy involved a linear sequence of 15 steps from 3-methyl-butanal (14 steps from chloro-dihydrocarvone) and did not need protecting groups. The synthetically challenging 1,5-butano­decahydro­naphthalene core was constructed efficiently via a type II intra­molecular [5+2] cycloaddition, followed by a unique ring-contraction cascade.

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2019-09-23
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