Enantioselective Construction of Tetrasubstituted Stereogenic Carbons through Brønsted Base Catalyzed Michael Reactions: α′-Hydroxy Enones as Key Enoate Equivalent

2014 ◽  
Vol 136 (51) ◽  
pp. 17869-17881 ◽  
Author(s):  
Eider Badiola ◽  
Béla Fiser ◽  
Enrique Gómez-Bengoa ◽  
Antonia Mielgo ◽  
Iurre Olaizola ◽  
...  
2007 ◽  
Vol 349 (16) ◽  
pp. 2454-2458 ◽  
Author(s):  
Weiping Ye ◽  
Zhiyong Jiang ◽  
Yujun Zhao ◽  
Serena Li Min Goh ◽  
Dasheng Leow ◽  
...  

2010 ◽  
Vol 352 (18) ◽  
pp. 3373-3379 ◽  
Author(s):  
Hongjun Liu ◽  
Wei Feng ◽  
Choon Wee Kee ◽  
Dasheng Leow ◽  
Wei-Tian Loh ◽  
...  

2018 ◽  
Vol 24 (28) ◽  
pp. 7217-7227 ◽  
Author(s):  
Joseba Izquierdo ◽  
Julen Etxabe ◽  
Eider Duñabeitia ◽  
Aitor Landa ◽  
Mikel Oiarbide ◽  
...  

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 Omega ◽  
2021 ◽  
Author(s):  
Kazuhiro Nagata ◽  
Chihiro Nakagawa ◽  
Wakana Yokoyama ◽  
Haruka Usui ◽  
Rikako Mochizuki ◽  
...  

2007 ◽  
Vol 269 (1-2) ◽  
pp. 214-217 ◽  
Author(s):  
Mihir K. Chaudhuri ◽  
Sahid Hussain

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