Copper‐Catalyzed Enantioselective Reductive Aldol Reaction of α,β‐Unsaturated Carboxylic Acids to Ketones: Silanes as Activator and Transient Protecting Group

Author(s):  
Hirotsugu Suzuki ◽  
Kenji Yoneoka ◽  
Sora Kondo ◽  
Takanori Matsuda
1980 ◽  
Vol 45 (6) ◽  
pp. 1655-1661 ◽  
Author(s):  
Robert Ponec

Various quantum chemical approaches to the problem of transmission of the substituent effect were compared. It was shown that inclusion of the electronic repulsion (field effect) was necessary to give a true picture of differences in ρ constants for reactions of the cis and trans isomers of substituted unsaturated carboxylic acids; the same holds for an adequate description of transmission of the substituent effect from the meta position on a given skeleton.


2020 ◽  
Vol 11 (21) ◽  
pp. 5572-5576 ◽  
Author(s):  
Noboru Hayama ◽  
Yusuke Kobayashi ◽  
Eriko Sekimoto ◽  
Anna Miyazaki ◽  
Kiyofumi Inamoto ◽  
...  

An asymmetric thia-Michael addition of arylthiols to α,β-unsaturated carboxylic acids using a thiourea catalyst that bears arylboronic acid and tertiary amine moieties is reported.


ChemInform ◽  
2009 ◽  
Vol 40 (12) ◽  
Author(s):  
Arun K. Ghosh ◽  
Jorden Kass ◽  
David D. Anderson ◽  
Xiaoming Xu ◽  
Christine Marian

ChemInform ◽  
2009 ◽  
Vol 40 (39) ◽  
Author(s):  
Minoru Kato ◽  
Hiroshi Oki ◽  
Kenichi Ogata ◽  
Shin-ichi Fukuzawa

2016 ◽  
Vol 55 (10) ◽  
pp. 3491-3495 ◽  
Author(s):  
Gang Li ◽  
Tao Wang ◽  
Fan Fei ◽  
Yi-Ming Su ◽  
Yan Li ◽  
...  

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