Oxo-Tethered Ruthenium(II) Complex as a Bifunctional Catalyst for Asymmetric Transfer Hydrogenation and H2Hydrogenation

2011 ◽  
Vol 133 (38) ◽  
pp. 14960-14963 ◽  
Author(s):  
Taichiro Touge ◽  
Tomohiko Hakamata ◽  
Hideki Nara ◽  
Tohru Kobayashi ◽  
Noboru Sayo ◽  
...  
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.


2018 ◽  
Vol 54 (94) ◽  
pp. 13244-13247 ◽  
Author(s):  
Xiaomin Shu ◽  
Ronghua Jin ◽  
Zhongrui Zhao ◽  
Tanyu Cheng ◽  
Guohua Liu

A bifunctional catalyst assembled by dual species manipulation presents high efficiency in Suzuki coupling-asymmetric transfer hydrogenation tandem reactions.


ChemInform ◽  
2012 ◽  
Vol 43 (12) ◽  
pp. no-no
Author(s):  
Taichiro Touge ◽  
Tomohiko Hakamata ◽  
Hideki Nara ◽  
Tohru Kobayashi ◽  
Noboru Sayo ◽  
...  

2016 ◽  
Vol 52 (35) ◽  
pp. 6005-6008 ◽  
Author(s):  
Jianyou Xu ◽  
Tanyu Cheng ◽  
Kun Zhang ◽  
Ziyun Wang ◽  
Guohua Liu

An active site-isolated organoruthenium-/organopalladium-functionalized yolk–shell-structured mesoporous silica is developed and its application in the one-pot enantioselective tandem Sonogashira coupling–asymmetric transfer hydrogenation of haloacetophenones and arylacetylenes to various chiral conjugated alkynols is investigated.


Catalysts ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 671
Author(s):  
Chad M. Bernier ◽  
Joseph S. Merola

A series of chiral complexes of the form Ir(NHC)2(aa)(H)(X) (NHC = N-heterocyclic carbene, aa = chelated amino acid, X = halide) was synthesized by oxidative addition of -amino acids to iridium(I) bis-NHC compounds and screened for asymmetric transfer hydrogenation of ketones. Following optimization of the reaction conditions, NHC, and amino acid ligands, high enantioselectivity was achieved when employing the Ir(IMe)2(l-Pro)(H)(I) catalyst (IMe = 1,3-dimethylimidazol-2-ylidene), which asymmetrically reduces a range of acetophenone derivatives in up to 95% enantiomeric excess.


Author(s):  
Pavel A. Dub ◽  
Nikolay V. Tkachenko ◽  
Vijyesh K. Vyas ◽  
Martin Wills ◽  
Justin S. Smith ◽  
...  

2003 ◽  
Vol 14 (16) ◽  
pp. 2481-2485 ◽  
Author(s):  
Pei Nian Liu ◽  
Ying Chun Chen ◽  
Xue Qiang Li ◽  
Yong Qiang Tu ◽  
Jin Gen Deng

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