4.4 Article

Chiral azabicyclo-N-oxyls mediated enantioselective electrooxidation of sec-alcohols

期刊

TETRAHEDRON LETTERS
卷 49, 期 36, 页码 5247-5251

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2008.06.112

关键词

chiral nitroxyl radical; enantioselective oxidation; optically active alcohol; electrooxidation

资金

  1. Ministry of Education, Science, Sports and Culture, Japan [19790017]
  2. Japan Society for the Promotion of Science [19550109]
  3. Konica Minolta Imaging Science Foundation, Japan.

向作者/读者索取更多资源

Enantiomerically pure azabicyclo-N-oxyls were prepared from L-hydroxyproline. They mediated enantioselective electrooxidation of racemic sec-alcohols to afford optically active sec-alcohols with moderate to high s value (up to 21) (C) 2008 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。

评论

主要评分

4.4
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据