Organocatalytic Asymmetric Domino Michael/Acyl Transfer Reaction Between α -Nitroketones and in situ- Generated ortho -Quinone Methides: Route to 2-(1-Arylethyl)phenols

2018 ◽  
Vol 360 (23) ◽  
pp. 4502-4508 ◽  
Author(s):  
Chandan Gharui ◽  
Debasmita Behera ◽  
Subhas Chandra Pan
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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