An expeditious chiral route to analogs of mevinolin and compactin
โ Scribed by Ta-Jyh Lee
- Publisher
- Elsevier Science
- Year
- 1985
- Tongue
- French
- Weight
- 135 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
The transformation of partially protected aldofuranoses into dienes by Wittig olefination of the anomeric center followed by either allylation or oxopalladation of alkoxy-l,2-propadienes is described. Ring-closing metathesis of the linear dienes gives rise to a variety of highly functionalized and c
An Expeditious Route to the Synthesis of Highly Functionalized Chiral Oxepins from Monosaccharides. -A novel and versatile route to highly functionalized chiral oxepins [cf. (VI) and (IX)] derived from partially protected aldofuranoses such as (I) is reported. The transformation proceeds via Wittig
## Abstract For Abstract see ChemInform Abstract in Full Text.