期刊
TETRAHEDRON LETTERS
卷 56, 期 1, 页码 146-149出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2014.11.045
关键词
Lycoricidine; Garner aldehyde; Aldol cyclization
资金
- CSIR network project, New Delhi, India [BSC 0120]
- CSIR
A highly efficient total synthesis of 3-epi-(+)-lycoricidine has been described for the first time from easily available (S)-Garner aldehyde with an overall yield of 7% in 20 steps. Stereoselective nucleophilic addition, Sharpless asymmetric dihydroxylation, Dess-Martin periodinane oxidation, intramolecular aldol cyclization, and Luche reduction are the salient features of this approach. (C) 2014 Elsevier Ltd. All rights reserved.
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