252377-13-2Relevant articles and documents
(Thiolan-2-yl)diphenylmethyl benzyl ether/N,N′-diarylurea cocatalyzed asymmetric aziridination of cinnamyl bromide and aryl aldimine
Wang, Shang-Hua,Chein, Rong-Jie
, p. 2607 - 2615 (2016)
A dual catalyst system using THT-based chiral sulfide 2a and H-bond donor 10a was developed for the asymmetric imino Corey-Chaykovsky reaction. Under the optimum reaction conditions, cinnamyl bromide reacted with a wide scope of N-diphenylphosphinic aldim
Enantioselective synthesis of diaryl aziridines using tetrahydrothiophene- based chiral sulfides as organocatalysts
Huang, Meng-Ting,Wu, Hsin-Yi,Chein, Rong-Jie
supporting information, p. 1101 - 1103 (2014/01/17)
This work describes catalytic and asymmetric aziridinations (15 examples, 95-98% ee) of benzyl bromide and imines via the imino Corey-Chaykovsky reaction using (thiolan-2-yl)diarylmethanol benzyl ether as an organocatalyst. The catalyst and analogues thereof were prepared through an expeditious and efficient synthetic route featuring a double nucleophilic substitution and Shi epoxidation as key steps.
Stereoselective synthesis of α-silylamines by the direct addition of silyl anions to activated imines
Ballweg, David M.,Miller, Rebecca C.,Gray, Danielle L.,Scheidt, Karl A.
, p. 1403 - 1406 (2007/10/03)
(Chemical Equation Presented) A highly efficient stereoselective synthesis of unusual α-silylamines via a direct silyl anion addition reaction is reported. This approach is convergent and avoids any problematic aza-Brook shifts of the anionic intermediate