Theoretical investigation on mechanism of asymmetric Michael addition of malononitrile to chalcones catalyzed by Cinchona alkaloid aluminium(iii) complex

2011 ◽  
Vol 9 (18) ◽  
pp. 6402 ◽  
Author(s):  
Zhishan Su ◽  
Hai Whang Lee ◽  
Chan Kyung Kim
2013 ◽  
Vol 54 (45) ◽  
pp. 6064-6066 ◽  
Author(s):  
Xin Huang ◽  
Wen-Bin Yi ◽  
Danash Ahad ◽  
Wei Zhang

Materials ◽  
2021 ◽  
Vol 14 (3) ◽  
pp. 600
Author(s):  
Mariola Zielińska-Błajet ◽  
Joanna Najdek

An efficient approach to the synthesis of chiral selenoureas consisting of Cinchona alkaloid scaffolds was described. The new selenoureas were assessed as bifunctional organocatalysts in the asymmetric Michael addition reactions under mild conditions. The best results were obtained for selenoureas bearing the 4-fluorophenyl group. These catalysts promoted the reactions with enantioselectivities of up to 96% ee. Additionally, the catalytic performance of the thiourea and selenourea counterpart was compared.


Author(s):  
Xiqiang Hou ◽  
Jiang-Bo Wen ◽  
Li Yan ◽  
Da-Ming Du

A highly efficient cinchona alkaloid‐derived squaramide catalysed asymmetric Michael/cyclization cascade reaction of 4‐ arylmethylidene‐2,3‐dioxopyrrolidines with 2‐isothiocyanato‐1‐indanones was successfully developed. This protocol provides an efficient and mild access to obtain indanone‐derived...


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