Absolute and Relative Configuration of Erythroskyrin
โ Scribed by Beutler, John A.; Hilton, Bruce D.; Clark, Patrick; Tempesta, Michael S.; Corley, David G.
- Book ID
- 126295239
- Publisher
- American Chemical Society
- Year
- 1988
- Tongue
- English
- Weight
- 318 KB
- Volume
- 51
- Category
- Article
- ISSN
- 0163-3864
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
Three novel cyclopropanoid guaianolides axivalin, ivaxillarin, and anhydroivaxillarin have been isolated from Iva axillaris Pursh. ssp. robustior, and were assigned gross structures I, II, and III, respectively.' To confirm the
The relative stability in solution of diastereomeric pseudopeptidic sulfoxides initially designed as FKBP inhibitors is used to assign the absolute conยฎguration at the sulfur atom. Decomposition is shown to occur via b-elimination of the corresponding sulfenic acid and alkene. Complementary studies