期刊
ORGANIC LETTERS
卷 5, 期 18, 页码 3169-3171出版社
AMER CHEMICAL SOC
DOI: 10.1021/ol034407v
关键词
-
资金
- NIGMS NIH HHS [GM28553] Funding Source: Medline
[GRAPHICS] A highly stereoselective intramolecular cycloaddition of an indole tethered to an aza-ortho-xylylene intermediate effects the rapid construction of a substantial portion of the ring system of the cytotoxic natural product communesin B. An analogous cycloaddition involving an orthoquinone methide intermediate provides an adduct that clearly revealed that the structural assignment for nomofungin was in error.
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