期刊
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
卷 2010, 期 21, 页码 4075-4087出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejoc.201000331
关键词
Natural products; Synthetic methods; Ring closing metathesis; Aurisides; Macrolides
资金
- French Ministere de la Recherche et de l'Enseignement Superieur
- European Union (EU) [503467]
- Universite de Lyon 1
- Centre National de la Recherche Scientifique (CNRS)
Two approaches based on the ring-closing metathesis reaction have been explored for the synthesis of the core structure of the marine natural products, the aurisides. The second approach, accomplished in a stereocontrolled manner, used both a Brown's allylation and an Evans' aldolisation, and finally a transannular ketalization to deliver a highly functionalized auriside analogue.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据