The structure of acumycin: A 16-membered ring macrolide antibiotic
β Scribed by Jon Clardy; Janet Finer-Moore; Larry Weiler; Don C. Wiley
- Publisher
- Elsevier Science
- Year
- 1981
- Tongue
- French
- Weight
- 534 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0040-4020
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π SIMILAR VOLUMES
## Recently we have reported a systematic 13 C NHR study on 16-membered q acrolide
Candidin,the heptaene macrolide antifungal antibiotic from Streptornvces viridoflavus';was recognised to be a mixture of three active principles all belonging to the %onarotnatic" subgroup of heptaenes 2,3 .The name candidin was retained for the main component of the antibiotic complex while the two
D-Glucose was converted to a backbone chain containing the appropriate functionalities an correc7 stereochemistry for the construction of the Cl-C9 fragment of the 16-membered ring macrolide antibiotics carknycin A and B and leuccqzin A3. Ieucctnycin AS and carkmycins A and B (magnamycins A and B) s