A new efficient chiral iridium catalyst for asymmetric transfer hydrogenation of ketones

2004 ◽  
Vol 218 (2) ◽  
pp. 153-156 ◽  
Author(s):  
Yan-Yun Li ◽  
Hui Zhang ◽  
Jian-Shan Chen ◽  
Xin-Li Liao ◽  
Zhen-Rong Dong ◽  
...  
2009 ◽  
Vol 307 (1-2) ◽  
pp. 149-153 ◽  
Author(s):  
Xue-Qin Zhang ◽  
Yan-Yun Li ◽  
Zhen-Rong Dong ◽  
Wei-Yi Shen ◽  
Zhi-Bo Cheng ◽  
...  

ChemInform ◽  
2005 ◽  
Vol 36 (33) ◽  
Author(s):  
Zhen-Rong Dong ◽  
Yan-Yun Li ◽  
Jian-Shan Chen ◽  
Bao-Zhu Li ◽  
Yan Xing ◽  
...  

2005 ◽  
Vol 7 (6) ◽  
pp. 1043-1045 ◽  
Author(s):  
Zhen-Rong Dong ◽  
Yan-Yun Li ◽  
Jian-Shan Chen ◽  
Bao-Zhu Li ◽  
Yan Xing ◽  
...  

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

Synlett ◽  
2006 ◽  
Vol 2006 (08) ◽  
pp. 1155-1160 ◽  
Author(s):  
Jianliang Xiao ◽  
Xiaohong Li ◽  
John Blacker ◽  
Ian Houson ◽  
Xiaofeng Wu

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