124929-29-9Relevant academic research and scientific papers
Enzymatic enantioselective aldol reactions of isatin derivatives with cyclic ketones under solvent-free conditions
Liu, Zhi-Qiang,Xiang, Zi-Wei,Shen, Zhou,Wu, Qi,Lin, Xian-Fu
, p. 156 - 160 (2014)
Nuclease p1 from Penicillium citrinum was observed to directly catalyze the asymmetric aldol reactions between isatin derivatives and cyclic ketones with high isolated yields (up to 95%) and moderate to good stereoselectivity (dr up to >99/1, ee up to 82%
(R)- and (S)-Proline-Derived Chiral Phosphoramides as Organo catalysts for the Enantiodivergent Aldol Reaction of Isatins with Cyclohexanone in the Presence of Water
Cruz-Hernández, Carlos,Hernández-González, Perla E.,Juaristi, Eusebio
supporting information, p. 1827 - 1840 (2018/02/14)
Novel organocatalysts derived from (R)- and (S)-proline and incorporating a chiral phosphoramide fragment were rationally designed and subsequently synthesized. These chiral compounds catalyze the enantioselective aldol addition reaction of cyclohexanone
In situ formed bifunctional primary amine-imine catalyst: Application to the construction of chiral tertiary alcohols through asymmetric aldol-type reaction
Mao, Zhijie,Zhu, Xi,Lin, Aijun,Li, Weipeng,Shi, Yan,Mao, Haibin,Zhu, Chengjian,Cheng, Yixiang
supporting information, p. 2029 - 2036 (2013/08/23)
An in situ formation method to obtain chiral bifunctional primary amine-imine catalysts from the C2-symmetric chiral diimines has been developed. The efficiency of this method in the construction of chiral tertiary alcohols which are valuable p
