期刊
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
卷 2013, 期 28, 页码 6317-6324出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejoc.201300623
关键词
Natural products; Spiro compounds; Cyclization; Total synthesis
资金
- Council of Scientific and Industrial Research (CSIR)
- University Grants Commission (UGC), New Delhi, India
A highly stereoselective total synthesis of attenols A and B is described. The salient features of this synthesis are the utilization of a reductive radical cyclization strategy for methyl center creation, a Prins cyclization/reductive opening cascade for anti-1,3-diol motif generation, and a double alkylation tosylmethyl isocyanide (TosMIC) strategy to construct the spiro acetal segment.
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
分享论文
