Ontology highlight
ABSTRACT:
SUBMITTER: He C
PROVIDER: S-EPMC9357209 | biostudies-literature | 2022 Aug
REPOSITORIES: biostudies-literature
Angewandte Chemie (International ed. in English) 20220706 32
A 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 act ...[more]