1298086-41-5Relevant academic research and scientific papers
Enantioselective oxidation of 1,2-diols with quinine-derived urea organocatalyst
Rong, Zi-Qiang,Pan, Hui-Jie,Yan, Hai-Long,Zhao, Yu
, p. 208 - 211 (2014/01/23)
Quinine-derived urea has been identified as a highly efficient organocatalyst for the enantioselective oxidation of 1,2-diols using bromination reagents as the oxidant. This simple procedure utilizes readily available reagents and operates at ambient temperature to yield a wide range of α-hydroxy ketones in good yield (up to 94%) and excellent enantioselectivity (up to 95% ee).
Benzaldehyde lyase catalyzed enantioselective self and cross condensation reactions of acetaldehyde derivatives
Ayhan, Peruze,Imek, Ilke,Ifi, Bure,Demir, Ayhan S.
supporting information; experimental part, p. 2602 - 2605 (2011/05/13)
Flexible protected 1,3,4-trihydroxy-2-butanone is synthesized in high enantiomeric excesses by using asymmetric homo- and cross- acyloin coupling of aliphatic aldehydes catalyzed by benzaldehyde lyase.
