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Updated: Dec 17, 2025

From a Natural Product to Its Biosynthetic Gene Cluster: A Demonstration Using Polyketomycin from Streptomyces diastatochromogenes Tü6028
Published on: January 13, 2017
Asymmetric Total Synthesis of the Naturally Occurring Antibiotic Anthracimycin
Emma K Davison1,2,3, Jared L Freeman1,3, Wanli Zhang4
1School of Chemical Sciences, University of Auckland, 23 Symonds Street, Auckland, 1010, New Zealand.
Abstract:
The first total synthesis of the potent antibiotic anthracimycin was achieved in 20 steps. The synthesis features an intramolecular Diels-Alder reaction to forge the trans-decalin moiety, and an unprecedented aldol reaction using a complex β-ketoester to provide the tricarbonyl motif. A Stork-Zhao olefination and Grubbs ring closing metathesis delivered the E/Z-diene and forged the macrocycle. The C2 configuration was set with a base-mediated epimerization, providing access to (-)-anthracimycin.
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