4.8 Article

Enantioselective Synthesis of Dihydrospiro[indoline-3,4′-pyrano[2,3-c]pyrazole] Derivatives via Michael/Hemiketalization Reaction

期刊

ORGANIC LETTERS
卷 18, 期 6, 页码 1354-1357

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.6b00287

关键词

-

资金

  1. Indo-French Centre for Promotion of Advanced Research (IFCPAR), New Delhi [IFC/4803-4]
  2. Council of Scientific & Industrial Research (CSIR)

向作者/读者索取更多资源

A new bifunctional squaramide organocatalyst derived from L-proline mediated the first enantioselective synthesis of dihydrospiro[indoline-3,4'-pyrano [2,3-c]pyrazole] derivatives in excellent enantioselectivity by reacting pyrazolones with isatylidine beta,gamma-unsaturated alpha-ketoester. This new catalyst outperformed widely used thioureas and squaramides in inducing enantioselectivity.

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

4.8
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