1257767-66-0Relevant articles and documents
Asymmetric α-amination of 3-substituted oxindoles using chiral bifunctional phosphine catalysts
Jin, Qiao-Wen,Chai, Zhuo,Huang, You-Ming,Zou, Gang,Zhao, Gang
, p. 725 - 731 (2016)
A highly enantioselective α-amination of 3-substituted oxindoles with azodicarboxylates catalyzed by amino acids-derived chiral phosphine catalysts is reported. The corresponding products containing a tetrasubstituted carbon center attached to a nitrogen
Highly enantioselective organocatalytic -amination reactions of aryl oxindoles: Developing designer multifunctional alkaloid catalysts
Bui, Tommy,Hernandez-Torres, Gloria,Milite, Ciro,Barbas, Carlos F.
supporting information; experimental part, p. 5696 - 5699 (2011/03/18)
An enantioselective -amination of aryl oxindoles catalyzed by a dimeric quinidine has been developed. The reaction is general, broad in substrate scope, and affords the desired products in good yields with good to excellent enantioselectivities. This stud