Abstract
AbstractA modular total synthesis of kibdelomycin is disclosed that should enable structure–activity relationship (SAR) studies of this interesting class of antibiotics. The route uses simple building blocks and addresses lingering questions about its structural assignment and relationship to amycolamicin, a recently described natural product reported to have a similar structure. Initial antibacterial assays reveal that both C‐22 epimers (the N‐glycosidic linkage) of the natural product have similar activity while structurally truncated analogs lose activity.
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