Kinetic Studies of the Asymmetric Transfer Hydrogenation of Imines with Formic Acid Catalyzed by Rh−Diamine Catalysts

2006 ◽  
Vol 10 (3) ◽  
pp. 457-463 ◽  
Author(s):  
Donna G. Blackmond ◽  
Melanie Ropic ◽  
Marijan Stefinovic
2019 ◽  
Vol 55 (65) ◽  
pp. 9633-9636 ◽  
Author(s):  
Wan Wang ◽  
Xinzheng Yang

Density functional theory calculations reveal a proton-coupled hydride transfer mechanism with the participation of formic acid for asymmetric transfer hydrogenation of pyruvic acid catalyzed by chiral Os complexes.


2020 ◽  
Vol 7 (8) ◽  
pp. 975-979 ◽  
Author(s):  
Bin He ◽  
Phannarath Phansavath ◽  
Virginie Ratovelomanana-Vidal

4-Quinolone derivatives were conveniently reduced to 1,2,3,4-tetrahydroquinoline-4-ols with excellent enantioselectivities through asymmetric transfer hydrogenation using a tethered rhodium complex and formic acid/triethylamine as the hydride source.


ChemInform ◽  
2005 ◽  
Vol 36 (37) ◽  
Author(s):  
Ikuo Kawasaki ◽  
Kazuya Tsunoda ◽  
Tomoko Tsuji ◽  
Tomoko Yamaguchi ◽  
Hiroki Shibuta ◽  
...  

2018 ◽  
Vol 5 (8) ◽  
pp. 1280-1283 ◽  
Author(s):  
Yangshan Li ◽  
Miao Wan ◽  
Shutao Sun ◽  
Zhongjun Fu ◽  
Haofei Huang ◽  
...  

A highly enantioselective method to chiral α-substituted 6H-benzo[c]chromenes through chiral imidodiphosphoric acid-catalyzed asymmetric transfer hydrogenation of ketals has been established.


2016 ◽  
Vol 14 (29) ◽  
pp. 6937-6941 ◽  
Author(s):  
Ji Zhou ◽  
Qian-Fan Zhang ◽  
Wei-Hao Zhao ◽  
Guo-Fang Jiang

A chiral phosphoric acid-catalyzed asymmetric transfer hydrogenation of 3-trifluoromethylthioquinolines was developed, providing chiral 2,3-disubstituted 1,2,3,4-tetrahydroquinoline derivatives containing a stereogenic trifluoromethylthio group with up to 99% enantioselectivity.


2015 ◽  
Vol 51 (60) ◽  
pp. 12115-12117 ◽  
Author(s):  
Siyu Guo ◽  
Peng Yang ◽  
Jianrong (Steve) Zhou

A nickel catalyst is used for asymmetric hydrogenation of electron-deficient olefins using formic acid as hydrogen source.


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