1365284-38-3Relevant academic research and scientific papers
Simple branched sulfur-olefins as chiral ligands for Rh-catalyzed asymmetric arylation of cyclic ketimines: Highly enantioselective construction of tetrasubstituted carbon stereocenters
Wang, Hui,Jiang, Tao,Xu, Ming-Hua
supporting information, p. 971 - 974 (2013/04/10)
New, simple, sulfinamide-based branched olefin ligands have been developed and successfully used in Rh-catalyzed asymmetric arylations of cyclic ketimines, providing efficient and highly enantioselective access to valuable benzosultams and benzosulfamidat
Asymmetric synthesis of (Triaryl)methylamines by rhodium-catalyzed addition of arylboroxines to cyclic N-sulfonyl ketimines
Nishimura, Takahiro,Noishiki, Akira,Chit Tsui, Gavin,Hayashi, Tamio
supporting information; experimental part, p. 5056 - 5059 (2012/05/05)
Asymmetric addition of arylboroxines to cyclic N-sulfonyl ketimines proceeded in the presence of a rhodium catalyst coordinated with a chiral diene ligand to give high yields of benzosultams, where a triaryl-substituted stereogenic carbon center was created with high enantioselectivity (93-99% ee). The chiral benzosultams were transformed into the chiral (triaryl)methylamines by breaking the cyclic structure.
