Reactions of 4‐Nitrophenyl 5‐substituted Furan‐2‐carboxylates with R 2 NH / R 2 NH 2 + in 20 mol% DMSO (aq): Effect of Aryl Group on the Acyl‐Transfer Reaction

2021 ◽  
Author(s):  
Sang Yong Pyun ◽  
Kyu Cheol Paik ◽  
Man So Han ◽  
Bong Rae Cho
Keyword(s):  
Transfer Reaction ◽  
Acyl Transfer ◽  
Aryl Group ◽  
Acyl Transfer Reaction

Organocatalytic asymmetric Michael/hemiketalization/acyl transfer reaction of 1,3-propanediones with (E)-2-(2-nitrovinyl)phenols

2019 ◽  
Vol 17 (7) ◽  
pp. 1718-1721 ◽  
Author(s):  
Nimisha Bania ◽  
Subhas Chandra Pan
Keyword(s):  
Transfer Reaction ◽  
Acyl Transfer ◽  
Keto Ester ◽  
Acyl Transfer Reaction

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.

Synthesis of strained cyclic peptides via an aza-Michael–acyl-transfer reaction cascade

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

Organocatalytic Asymmetric Conjugate Addition and Cascade Acyl Transfer Reaction of α-Nitroketones

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

scholarly journals Organocatalytic Asymmetric Michael/Acyl Transfer Reaction between α-Nitroketones and 4-Arylidene- pyrrolidine-2,3-diones

2021 ◽  
Author(s):  
Chandrakanta Parida ◽  
Subhas C Pan
Keyword(s):  
Transfer Reaction ◽  
Acyl Transfer ◽  
Reaction Conditions ◽  
Acyl Transfer Reaction

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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