## 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
ChemInform Abstract: A Rapid Formal Synthesis of the Macrolide (-)-A26771B.
β Scribed by Woo-Wha Lee; Hyun Jung Shin; Sukbok Chang
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 32 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
A Formal Total Synthesis of (Β±)-Homogynolide-B. -The key intermediate keto ketals (III) and (IV), derived from ester (I), are further converted in a separate way to the target spirolactone (XIII), the Greene's precursor of homogynolide-B. The 5-exo-dig radical cyclization of the bromo acetal (X) fo
## 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
A Formal Synthesis of (+)-Brefeldin A. -An advanced synthetic intermediate for (+)-brefeldin A (IX) is efficiently synthesized from Weinreb amide (I). The procedure involves the highly stereoselective construction of the hydroxycyclopentane moiety via an oxabicycloheptanone unit. -(SUH,