1310339-16-2Relevant academic research and scientific papers
8-Amino-5,6,7,8-tetrahydroquinolines as ligands in iridium(III) catalysts for the reduction of aryl ketones by asymmetric transfer hydrogenation (ATH)
Zerla, Daniele,Facchetti, Giorgio,Fusè, Marco,Pellizzoni, Michela,Castellano, Carlo,Cesarotti, Edoardo,Gandolfi, Raffaella,Rimoldi, Isabella
, p. 1031 - 1037 (2014/08/18)
Aqua iridium(III) complexes with 8-amino-5,6,7,8-tetrahydroquinolines CAMPY L1 and its derivatives as chiral ligands proved to be very efficient catalysts for the reduction of a wide range of prochiral aryl ketones, revealing a variety of behaviours in te
Dynamic kinetic resolution of β′-keto-β-amino esters using Ru-DTBM-Sunphos catalyzed asymmetric hydrogenation
Li, Xiaoming,Tao, Xiaoming,Ma, Xin,Li, Wanfang,Zhao, Mengmeng,Xie, Xiaomin,Ayad, Tahar,Ratovelomanana-Vidal, Virginie,Zhang, Zhaoguo
, p. 7152 - 7156 (2013/07/26)
A convenient method for the enantioselective synthesis of β′-hydroxy-β-amino esters was developed through intensive investigations of the reaction conditions. Dichloromethane (DCM)/2,2,2- trifluoroethanol (TFE) and 1,2-dichloroethane (DCE)/TFE combination
3-(Hydroxy(phenyl)methyl)azetidin-2-ones obtained via catalytic asymmetric hydrogenation or by biotransformation
Rimoldi, Isabella,Cesarotti, Edoardo,Zerla, Daniele,Molinari, Francesco,Albanese, Domenico,Castellano, Carlo,Gandolfi, Raffaella
, p. 597 - 602 (2011/06/21)
The catalytic asymmetric reduction of ethyl-2-(benzamidomethyl)-3-oxo- phenylpropanoate was realized with high enantiomeric and diastereoisomeric excesses via biotransformation using whole cells of different yeasts and asymmetric hydrogenation with Ru(II)
