1059698-75-7Relevant academic research and scientific papers
A novel chiral surfactant-type metallomicellar catalyst for asymmetric Michael addition in water
Liang, Xinping,Gui, Yang,Li, Kuiliang,Li, Jindong,Zha, Zhenggen,Shi, Lei,Wang, Zhiyong
supporting information, p. 11118 - 11121 (2020/10/05)
A series of Schiff-based ligands consisting of both tertiary amines and lipophilic groups were designed and synthesized. Using these ligands, a new chiral surfactant-type metallomicellar catalyst was developed in water, and this was identified by SEM/TEM analyses. These metallomicelles can be empolyed in asymmetric Michael addition reactions in water, delivering the corresponding adducts with excellent yields and enantioselectivities.
Highly enantioselective Friedel-Crafts reaction of indoles with 2-enoylpyridine 1-oxides catalyzed by chiral pyridine 2,6-bis(5′,5′- diphenyloxazoline)-Cu(II) complexes
Singh, Pradeep K.,Singh, Vinod K.
supporting information; experimental part, p. 4121 - 4124 (2009/05/27)
(Chemical Equation Presented) The catalytic enantioselective Friedel-Crafts reaction of indoles with 2-enoylpyridine 1-oxides has been studied in the presence of chiral pyridine 2,6-bis(5′,5′-diphenyloxazoline)-Cu(II) complexes. The reaction furnished alk
