Journal
CHEMICAL COMMUNICATIONS
Volume -, Issue 46, Pages 7113-7115Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/b912733j
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Funding
- Deutsche Forschungsgemeinschaft
- Fonds der Chemischen Industrie
- International Max Planck Research School Chemical Biology (IMPRS-CB)
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The natural product thiopeptide antibiotic thiostrepton is shown to undergo facile epimerization at its thiazoline residue in favor of the naturally observed D-configuration, suggesting that a classical epimerase enzyme may not be involved in its biosynthesis.
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