Enantiocontrolled Construction of Functionalized Tetrahydrofurans: Total Synthesis of (6S,7S,9R,10R)-6,9-Epoxynonadec-18-ene-7,10diol, a Marine Natural Product. -A new strategy for the construction of highly functionalized tetrahydrofurans via the key bis-C 3 building block (III) is developed and ap
Enantiocontrolled Construction of Functionalized Tetrahydrofurans: Total Synthesis of (6 S ,7 S ,9 R ,10 R )-6,9-Epoxynonadec-18-ene-7,10-diol, a Marine Natural Product
β Scribed by Wang, Zhi-Min; Shen, Ming
- Book ID
- 126245809
- Publisher
- American Chemical Society
- Year
- 1998
- Tongue
- English
- Weight
- 71 KB
- Volume
- 63
- Category
- Article
- ISSN
- 0022-3263
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
The stereocontrolled synthesis of (6S,7S,9R, 10R)-6,9-epoxynonadec-18-ene-7,10-diol, isolated from the brown alga, Notheia anomala, has been achieved. The key 2,3,5-trisubstituted tetrahydrofuran ring was constructed by alkylation of the sulfonyl-stabilized oxiranly anion followed by 5-endo cyclizat
## 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