ChemInform Abstract: Broensted Acid Enhanced Rhodium-Catalyzed Conjugate Addition of Aryl C-H Bonds to α,β-Unsaturated Ketones under Mild Conditions.

ChemInform ◽  
2013 ◽  
Vol 44 (1) ◽  
pp. no-no
Author(s):  
Lei Yang ◽  
Bo Qian ◽  
Hanmin Huang
2011 ◽  
Vol 233-235 ◽  
pp. 977-984
Author(s):  
Bin Wang ◽  
Chen Jiang Liu

Brønsted acidic ionic liquids based on benzimidazolium cation was synthesized and employed as an efficient catalysts for the Michael addition reaction of indoles to α,β-unsaturated ketones under mild conditions to afford the corresponding conjugate addition products in high yields (90%-98%). The catalyst 1-butyl-3-(3-sulfopropyl)benzimidazolium p-toluenesulfonate ([PSbbim][p-CH3PhSO3]) could be reused at least three times without a noticeably decrease in its activity.


1980 ◽  
Vol 45 (15) ◽  
pp. 3053-3061 ◽  
Author(s):  
Jeffrey Schwartz ◽  
Denise B. Carr ◽  
Robert T. Hansen ◽  
Fabian M. Dayrit

2017 ◽  
Vol 15 (19) ◽  
pp. 4191-4198 ◽  
Author(s):  
Haojiang Wang ◽  
Yifeng Wang ◽  
Cheng Zhang ◽  
Yidong Jiang ◽  
Mingming Chu ◽  
...  

A highly enantioselective conjugate addition of 2-substituted benzofuran-3(2H)-ones to α,β-unsaturated ketones promoted by chiral copper complexes has been developed.


2018 ◽  
Vol 150 (2) ◽  
pp. 295-302
Author(s):  
Bernard Mravec ◽  
Kristína Plevová ◽  
Radovan Šebesta

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