40610-41-1Relevant academic research and scientific papers
Enantioselective C-H Olefination of α-Hydroxy and α-Amino Phenylacetic Acids by Kinetic Resolution
Xiao, Kai-Jiong,Chu, Ling,Yu, Jin-Quan
supporting information, p. 2856 - 2860 (2016/02/27)
Significant progress has been made in the past decade regarding the development of enantioselective C-H activation reactions by desymmetrization. However, the requirement for the presence of two chemically identical prochiral C-H bonds represents an inherent limitation in scope. Reported is the first example of kinetic resolution by a palladium(II)-catalyzed enantioselective C-H activation and C-C bond formation, thus significantly expanding the scope of enantioselective C-H activation reactions.
Synthesis and enantiomeric recognition studies of a novel 5,5-dioxophenothiazine-1,9 bis(thiourea) containing glucopyranosyl groups
Kormos, Attila,Móczár, Ildikó,Pál, Dávid,Baranyai, Péter,Kupai, József,Tóth, Klára,Huszthy, Péter
, p. 62 - 65 (2013/02/25)
A novel optically active 5,5-dioxophenothiazine-1,9 bis(thiourea) containing glucopyranosyl groups was synthesized and its enantiomeric recognition properties were examined towards the enantiomers of tetrabutylammonium salts of chiral α-hydroxy and N-protected α-amino acids using UV-vis spectroscopy.
