期刊
ORGANIC & BIOMOLECULAR CHEMISTRY
卷 15, 期 28, 页码 5908-5911出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c7ob00950j
关键词
-
资金
- Indian Institute of Technology Madras, Chennai
- CSIR-INDIA [02(0209)/14/EMR-II]
- IIT Madras, Chennai
An efficient and mild synthetic strategy for the total synthesis of selaginpulvilin D has been reported. A highly chemoselective enyne-alkyne dehydro Diels-Alder reaction has been employed for the construction of the tricyclic fluorene framework present in the natural product selaginpulvilin D. An improved overall yield (10.5%) has been achieved for selaginpulvilin D, starting from commercially available m-anisaldehyde in 9 linear, operationally simple synthetic transformations.
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