Squaramide‐catalysed asymmetric cascade Michael addition/acyl transfer reaction between unsaturated benzothiophenones and α-nitroketones

Author(s):  
Cheng Niu ◽  
Da-Ming Du

An efficient and practical organocatalytic asymmetric strategy was developed using unsaturated benzothiophenones and α‐nitroketones catalysed by bifunctional squaramide via Michael addition and acyl transfer steps. A broad range of chiral...

2019 ◽  
Vol 17 (7) ◽  
pp. 1718-1721 ◽  
Author(s):  
Nimisha Bania ◽  
Subhas Chandra Pan

An organocatalytic asymmetric cascade Michael/hemiketalization/acyl transfer reaction between (E)-2-(2-nitrovinyl)phenols and 1,3-propanediones is disclosed to generate products having keto, ester and nitro functionalities.


2012 ◽  
Vol 48 (65) ◽  
pp. 8084 ◽  
Author(s):  
Jochem P. A. Rutters ◽  
Yvette Verdonk ◽  
Remko de Vries ◽  
Steen Ingemann ◽  
Henk Hiemstra ◽  
...  

2011 ◽  
Vol 76 (15) ◽  
pp. 6230-6239 ◽  
Author(s):  
Rui-jiong Lu ◽  
Yun-yun Yan ◽  
Jin-jia Wang ◽  
Quan-sheng Du ◽  
Shao-zhen Nie ◽  
...  

2021 ◽  
Author(s):  
Chandrakanta Parida ◽  
Subhas C Pan

An organocatalytic asymmetric Michael/acyl transfer reaction between α-nitroketones and 4-arylidene-pyrrolidine-2,3-diones was reported. Bifunctional thiourea catalyst was found to be effective for this reaction. With 10 mol% of the catalyst, good results were attained for a variety of 1,5-dihydro-2H-pyrrol-2-ones under mild reaction conditions.


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