ChemInform Abstract: Enantioselective Bimetallic Catalysis of Michael Additions Forming Quaternary Stereocenters.

ChemInform ◽  
2009 ◽  
Vol 40 (11) ◽  
Author(s):  
Sascha Jautze ◽  
Rene Peters
2010 ◽  
Vol 352 (18) ◽  
pp. 3364-3372 ◽  
Author(s):  
Rubén Manzano ◽  
José M. Andrés ◽  
María D. Muruzábal ◽  
Rafael Pedrosa

2020 ◽  
Vol 24 (7) ◽  
pp. 746-773
Author(s):  
Péter Bakó ◽  
Tamás Nemcsok ◽  
Zsolt Rapi ◽  
György Keglevich

: Many catalysts were tested in asymmetric Michael additions in order to synthesize enantioenriched products. One of the most common reaction types among the Michael reactions is the conjugated addition of malonates to enones making it possible to investigate the structure–activity relationship of the catalysts. The most commonly used Michael acceptors are chalcone, substituted chalcones, chalcone derivatives, cyclic enones, while typical donors may be dimethyl, diethyl, dipropyl, diisopropyl, dibutyl, di-tert-butyl and dibenzyl malonates. This review summarizes the most important enantioselective catalysts applied in these types of reactions.


ACS Catalysis ◽  
2021 ◽  
pp. 858-864
Author(s):  
Rong-Hua Wang ◽  
Jiang-Fei Li ◽  
Yue Li ◽  
Shao-Long Qi ◽  
Tao Zhang ◽  
...  
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