4.7 Article

Stable and Reusable Palladium Nanoparticles-Catalyzed Conjugate Addition of Aryl Iodides to Enones: Route to Reductive Heck Products

期刊

ADVANCED SYNTHESIS & CATALYSIS
卷 359, 期 21, 页码 3741-3751

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adsc.201700823

关键词

conjugate addition; palladium nanocatalyst; reductive Heck reaction; reusable catalysts; beta-substituted carbonyl compounds

资金

  1. IIT Madras for Exploratory Research Project [CHY/16-17/846/RFER/GSEK]
  2. UGC, New Delhi
  3. IIT Madras

向作者/读者索取更多资源

An efficient, binaphthyl-backbone-stabilized palladium nanoparticles (Pd-BNP) catalyst for the 1,4-addition of aryl halides to enones has been developed. The scope of the reaction has been studied with various substituted and sterically hindered aryl halides and enones to afford the conjugate addition products in good to excellent yields. The catalyst has been recovered and reused up to five times without any appreciable change in particle size or reactivity.

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

4.7
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