On the absolute configuration of the synthetic macrolide patulolide C
β Scribed by Gezina Beurskens; J. M. M. Smits; Paul T. Beurskens; L. Thijs; D. M. Egenberger; B. Zwanenburg
- Publisher
- Springer
- Year
- 1989
- Tongue
- English
- Weight
- 239 KB
- Volume
- 19
- Category
- Article
- ISSN
- 1572-8854
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π SIMILAR VOLUMES
As a result of the x-ray single crystal analysis of N-iodoacetylamphotericin B the chemical and stereochemical absolute structure ia presented (I). A similar etructure and stereochemistry wae extended to the parent compound itself, amphotericin B, a heptaene macrolide antifungal antibiotic possessin
Tetrahedron Letters No. 41. pp. 3601-3604 (1970) p. 3529 W. Sprenger was omitted from the "Contributors to this issue" W. MECHLINSKI, C. P. SCHAFFNER, P. GANIS and G. AVITABILE: Structure and absolute configuration of the polyene macrolide antibiotic amphotericin B.
The absolute stereochemistry of the secondary alcohol of the 1,2-dihydroxybutenyl substituent of ciguatoxin (1) was shown to be S by comparing the split CD curve of ciguatoxin tetra-p-bromobenzoate (2) with those of di-and tri-p-bromobenzoates of AB ring fragments that were synthesized enantioselect