4.4 Article

Enantioselective synthesis of martinelline chiral core and its diastereomer using asymmetric tandem Michael-aldol reaction

期刊

TETRAHEDRON
卷 64, 期 51, 页码 11568-11579

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tet.2008.10.032

关键词

Martinelline; Martinellic acid; Tandem Michael-aldol reaction; Organocatalyst; Asymmetric synthesis

资金

  1. Ministry of Education, Culture, Sports, Science and Technology, Japan

向作者/读者索取更多资源

The martinelline chiral core 3 and its disastereomer were synthesized by using the asymmetric tandem Michael-aldol reaction as the key step from 4-methyoxycarbonylanthranilaldehyde and the alpha,beta-unsatuarated aldehyde (C) 2008 Published by Elsevier Ltd.

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