期刊
NATURE CHEMISTRY
卷 1, 期 3, 页码 225-228出版社
NATURE PUBLISHING GROUP
DOI: 10.1038/NCHEM.215
关键词
-
资金
- Alexander von Humboldt Foundation
- Max Planck Society
- Deutsche Forschungsgemeinschaft
- Fonds der Chemischen Industrie
Cascade reactions enable the rapid build-up of molecular complexity from relatively simple starting materials. Both rapid construction and the ability to prepare related structures are crucial to the study of biological activities. Here, we report an efficient, highly enantioselective and diastereoselective total synthesis of ricciocarpin A. The key feature of the synthesis is a one-pot, three-step, organocatalytic reductive Michael-Tishchenko cascade. The conciseness and flexibility of this approach not only resulted in the synthesis of the natural product, but also of its antipode and four other structural analogues. A preliminary biological evaluation of these compounds identified an analogue with significantly improved molluscicidal activity.
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