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- W2070546871 endingPage "12833" @default.
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- W2070546871 abstract "A straightforward access to polyhydroxylated terpenoids based on two key titanocene(III)-mediated reactions is presented: the “head-to-tail” Barbier-type addition of prenyl chlorides to α,β-unsaturated aldehydes, which allows the introduction of hydroxy groups at desirable positions of the acyclic precursor, and the subsequent bioinspired radical cyclisation. This methodology has been also used in the first total synthesis of pentacyclic sesterstatin 1 and a model compound of the C–D rings of aspergilloxide." @default.
- W2070546871 created "2016-06-24" @default.
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- W2070546871 creator A5062545081 @default.
- W2070546871 creator A5076282994 @default.
- W2070546871 date "2012-08-24" @default.
- W2070546871 modified "2023-10-17" @default.
- W2070546871 title "Combining the Power of Ti<sup>III</sup>-Mediated Processes for Easy Access to Hydroxylated Polycyclic Terpenoids: Synthesis of Sesterstatin 1 and C-D Rings of Aspergilloxide" @default.
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