## Abstract The total synthesis of (+)β9β__epi__βdictyostatin (**1b**), a diastereomer of the antimitotic marineβspongeβderived macrolide (β)βdictyostatin (**1a**), was achieved by creating 11 stereogenic centers and 4 stereogenic double bonds with a high level of stereocontrol. The yield for the 2
Total synthesis of verrucarol: a stereoselective synthesis of 13,14-dinor-15-hydroxytrichothec-9-ene
β Scribed by Roush, William R.; D'Ambra, Thomas E.
- Book ID
- 126402275
- Publisher
- American Chemical Society
- Year
- 1980
- Tongue
- English
- Weight
- 417 KB
- Volume
- 45
- Category
- Article
- ISSN
- 0022-3263
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π SIMILAR VOLUMES
A rather facile stereoselective total synthesis of (9S)-9-dihydroerythronolide A starting from D-glucose was achieved via coupling of Cl-C6 and C7-Cl5 segments and subsequent macrolactonizotion. The well known macrolide antibiotic erythromycin A (1) has been an attractive synthetic target for moder
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v