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Issue 4, 2017
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Biomimetic total synthesis of (±)-berkeleyamide D

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Abstract

We describe the total synthesis of (±)-berkeleyamide D using a biosynthetically inspired strategy. The spirocyclic core of berkeleyamide D was constructed via sequential epoxidations and a late-stage base-mediated cyclization of a biosynthetically relevant precursor. Our synthetic solution might be applicable to access other fungal natural products of this family.

Graphical abstract: Biomimetic total synthesis of (±)-berkeleyamide D

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Publication details

The article was received on 14 Dec 2016, accepted on 13 Jan 2017 and first published on 13 Jan 2017


Article type: Research Article
DOI: 10.1039/C6QO00812G
Citation: Org. Chem. Front., 2017,4, 506-509
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    Biomimetic total synthesis of (±)-berkeleyamide D

    D. Jo and S. Han, Org. Chem. Front., 2017, 4, 506
    DOI: 10.1039/C6QO00812G

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