Chiral Induction Effects in Ruthenium(II) Amino Alcohol Catalysed Asymmetric Transfer Hydrogenation of Ketones: An Experimental and Theoretical Approach

Author(s):  
Daniëlle G. I. Petra ◽  
Joost N. H. Reek ◽  
Jan-Willem Handgraaf ◽  
Evert Jan Meijer ◽  
Peter Dierkes ◽  
...  
ChemInform ◽  
2010 ◽  
Vol 31 (11) ◽  
pp. no-no
Author(s):  
Danielle G. I. Petra ◽  
Paul C. J. Kamer ◽  
Piet W. N. M. van Leeuwen ◽  
Kees Goubitz ◽  
Arjen M. Van Loon ◽  
...  

ChemInform ◽  
2011 ◽  
Vol 42 (29) ◽  
pp. no-no
Author(s):  
Mei-Ling Han ◽  
Xiang-Ping Hu ◽  
Jia-Di Huang ◽  
Li-Gong Chen ◽  
Zhuo Zheng

ChemInform ◽  
2010 ◽  
Vol 27 (22) ◽  
pp. no-no
Author(s):  
J. TAKEHARA ◽  
S. HASHIGUCHI ◽  
A. FUJII ◽  
S. INOUE ◽  
T. IKARIYA ◽  
...  

Proceedings ◽  
2019 ◽  
Vol 41 (1) ◽  
pp. 63
Author(s):  
Anna Kmieciak ◽  
Marek P. Krzemiński

Monoterpenes are optically active compounds which occur in nature. This fact makes them interesting precursors for the synthesis of optically active ligands, which can be applied in various asymmetric reactions. In this work, we present the synthesis of optically pure 2-amino-apopinan-3-ol from (−)-α-pinene. The obtained amino alcohol was used as a precursor of oxazaborolidine, which was used as catalyst in the asymmetric reduction of aryl-alkyl ketones with borane. In the second part, we transformed 2-amino-apopinan-3-ol into PHOX ligand in a three-step reaction. The complex of ruthenium precursor with PHOX ligand was used as a catalyst in the asymmetric transfer hydrogenation of aryl-alkyl ketones. Alcohols with enantiomeric excesses of up to 97% were isolated using both reduction methods.


1996 ◽  
pp. 233 ◽  
Author(s):  
Jun Takehara ◽  
Shohei Hashiguchi ◽  
Akio Fujii ◽  
Shin-ichi Inoue ◽  
Takao Ikariya ◽  
...  

Author(s):  
Daniëlle G. I. Petra ◽  
Paul C. J. Kamer ◽  
Piet W. N. M. van Leeuwen ◽  
Kees Goubitz ◽  
Arjen M. Van Loon ◽  
...  

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