Home > Papers

 
 
Enantioselective Michael addition of 2,4-pentanedione To nitroalkenes catalyzed by dehydroabietylamine-cinchonine-squaramide
PENG Xueke,ZHENG Jie,DONG Chune *
School of Pharmaceutical Science, Wuhan University
*Correspondence author
#Submitted by
Subject:
Funding: none
Opened online:18 April 2018
Accepted by: none
Citation: PENG Xueke,ZHENG Jie,DONG Chune.Enantioselective Michael addition of 2,4-pentanedione To nitroalkenes catalyzed by dehydroabietylamine-cinchonine-squaramide[OL]. [18 April 2018] http://en.paper.edu.cn/en_releasepaper/content/4744456
 
 
In this paper, on the basis of the special activity of natural rosin derivatives and the good asymmetric induction activity of squaramide organic catalysts, a novel dehydroabietylamine-cinchonine-squaramide catalyst has been developed for asymmetric Michael addition of 2,4-pentanedione to nitroalkenes. It found that with using 5 mol% dehydroabietylamine-cinchonine-squaramide catalyst , the reaction of 2,4-pentanedione to nitroalkenes could act effectively, and a series of nitroalkene derivatives possessing optical activity were afforded with high reaction yields and excellent enantioselectivities (up to 99% yield, 89% ee).
Keywords:Organic chemistry; Dehydroabietylamine-cinchonine-squaramide; Michael addition; Nitroalkenes
 
 
 

For this paper

  • PDF (0B)
  • ● Revision 0   
  • ● Print this paper
  • ● Recommend this paper to a friend
  • ● Add to my favorite list

    Saved Papers

    Please enter a name for this paper to be shown in your personalized Saved Papers list

Tags

Add yours

Related Papers

Statistics

PDF Downloaded 44
Bookmarked 0
Recommend 0
Comments Array
Submit your papers