4.0 Article

Acid-base organocatalysts for the aza-Morita-Baylis-Hillman reaction of nitroalkenes

期刊

TETRAHEDRON-ASYMMETRY
卷 21, 期 8, 页码 891-894

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetasy.2010.05.027

关键词

-

资金

  1. Ministry of Education, Culture, Sports, Science and Technology, Japan
  2. Takeda Science Foundation
  3. Grants-in-Aid for Scientific Research [22790010] Funding Source: KAKEN

向作者/读者索取更多资源

A new class of acid-base chiral organocatalysts 1a and 2 for aza-Morita-Baylis-Hillman (aza-MBH) reaction of conjugated nitroalkenes is described. The acidic phenolic hydroxy groups and basic imidazole unit cooperatively activate nitroalkenes to promote the aza-MBH reaction in good yields with moderate enantioselectivities. (C) 2010 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

4.0
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