A concise total synthesis of (±)-cipadonoid B from synthetic azedaralide†
Abstract
The tetranortriterpene cipadonoid B was efficiently constructed from synthetic azedaralide in a one-pot cascade, via the underutilised ketal-Claisen rearrangement.
* Corresponding authors
a
School of Chemistry and Molecular Biosciences, University of Queensland, Brisbane, Queensland, Australia
E-mail:
c.williams3@uq.edu.au
The tetranortriterpene cipadonoid B was efficiently constructed from synthetic azedaralide in a one-pot cascade, via the underutilised ketal-Claisen rearrangement.
J. M. Faber and C. M. Williams, Chem. Commun., 2011, 47, 2258 DOI: 10.1039/C0CC04698A
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