Asymmetric transfer hydrogenation reactions of N-sulfonylimines by using alcohols as hydrogen sources

2018 ◽  
Vol 54 (39) ◽  
pp. 4963-4966 ◽  
Author(s):  
Fan Yang ◽  
Jingchao Chen ◽  
Guoli Shen ◽  
Xuexin Zhang ◽  
Baomin Fan

A palladium/zinc co-catalytic system was established and successfully utilized in the asymmetric transfer hydrogenation reactions of N-sulfonylimines with alcohols as hydrogen sources.

2011 ◽  
Vol 9 (1) ◽  
pp. 175-179 ◽  
Author(s):  
Zhongqiang Zhou ◽  
Yong Sun ◽  
Aiqing Zhang

AbstractChiral aminosulfonamides containing imidazolium group were used as ligands for the ruthenium(II)-catalyzed asymmetric transfer hydrogenation of prochiral ketones in ionic liquid, affording good to excellent conversions and enantiomeric excesses. The catalytic system could be easily recovered and reused several times.


2019 ◽  
Vol 55 (90) ◽  
pp. 13578-13581 ◽  
Author(s):  
Zhongrui Zhao ◽  
Fengwei Chang ◽  
Tao Wang ◽  
Lijian Wang ◽  
Lingbo Zhao ◽  
...  

A magnetically recyclable bifunctional catalyst enables synergistic Suzuki cross-coupling/asymmetric transfer hydrogenation and successive reduction/asymmetric transfer hydrogenation reactions for the preparation of chiral aromatic alcohols.


2007 ◽  
Vol 692 (10) ◽  
pp. 1875-1891 ◽  
Author(s):  
Thengarai S. Venkatakrishnan ◽  
Swadhin K. Mandal ◽  
Raghuraman Kannan ◽  
Setharampattu S. Krishnamurthy ◽  
Munirathinam Nethaji

2016 ◽  
Vol 45 (20) ◽  
pp. 8513-8531 ◽  
Author(s):  
Pau Clavero ◽  
Arnald Grabulosa ◽  
Mercè Rocamora ◽  
Guillermo Muller ◽  
Mercè Font-Bardia

Optically pure P-stereogenic monophosphorus ligands containing a heterocyclic substituent have been prepared. They have been coordinated to Ru-η6-arene moieties in which the ligands act as mono- or bidentate. The complexes catalyse asymmetric transfer hydrogenation reactions with up to 70% ee.


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