scholarly journals Titelbild: Catalyst-Enabled Site-Divergent Stereoselective Michael Reactions: Overriding Intrinsic Reactivity of Enynyl Carbonyl Acceptors (Angew. Chem. 17/2018)

2018 ◽  
Vol 130 (17) ◽  
pp. 4519-4519
Author(s):  
Daisuke Uraguchi ◽  
Ryo Shibazaki ◽  
Naoya Tanaka ◽  
Kohei Yamada ◽  
Ken Yoshioka ◽  
...  
2018 ◽  
Vol 57 (17) ◽  
pp. 4431-4431
Author(s):  
Daisuke Uraguchi ◽  
Ryo Shibazaki ◽  
Naoya Tanaka ◽  
Kohei Yamada ◽  
Ken Yoshioka ◽  
...  

2018 ◽  
Vol 57 (17) ◽  
pp. 4732-4736 ◽  
Author(s):  
Daisuke Uraguchi ◽  
Ryo Shibazaki ◽  
Naoya Tanaka ◽  
Kohei Yamada ◽  
Ken Yoshioka ◽  
...  

2018 ◽  
Vol 130 (17) ◽  
pp. 4822-4826 ◽  
Author(s):  
Daisuke Uraguchi ◽  
Ryo Shibazaki ◽  
Naoya Tanaka ◽  
Kohei Yamada ◽  
Ken Yoshioka ◽  
...  

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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