Chiralyst® Rh640
Chiralyst® Rh640
Applications & references
Description
Asymmetric reduction of α-sulfonyloxy acetophenone compound yielding an optically active 2-sulfonyloxy-1-phenylethanol derivative with high enantiomer excess.
Reference: WO2008 054155
Transfer hydrogenation of aromatic ß-ketoester for the synthesis of secondary aminoalcohols.
Reference: WO2005 028437
Asymmetric transfer hydrogenation of N-sulfonyl ketimine derivatives.
Reference: Tetrah. Asym. 2010, 21, 800 (DOI: 10.1016/j.tetasy.2010.04.047)
Asymmetric transfer hydrogenation of 2-tosyloxy-1-(4-hydroxyphenyl)ethanones derivatives leading to an efficient synthetic route of ß-adrenergic agonists.
Reference: Tetrah. Asym. 2007, 18, 2662 (DOI: 10.1016/j.tetasy.2007.10.046)