17879-98-0Relevant articles and documents
Regiodivergent and Stereospecific Aziridine Opening by Copper-Catalyzed Addition of Silicon Grignard Reagents
Yi, Hong,Oestreich, Martin
supporting information, p. 6505 - 6507 (2019/04/30)
A stereospecific ring opening of various 2-aryl-substituted aziridines with silicon Grignard reagents under copper catalysis is reported. The regiochemical outcome is governed by the steric demand of the silicon nucleophile. The LiCl introduced with the m
Alkene functionalization for the stereospecific synthesis of substituted aziridines by visible-light photoredox catalysis
Yu, Wan-Lei,Chen, Jian-Qiang,Wei, Yun-Long,Wang, Zhu-Yin,Xu, Peng-Fei
, p. 1948 - 1951 (2018/03/01)
A novel strategy involving visible-light-induced functionalization of alkenes for the synthesis of substituted aziridines was developed. The readily prepared N-protected 1-aminopyridinium salts were used for the generation of N-centered radicals. This approach allowed the synthesis of aziridines bearing various functional groups with excellent diastereoselectivity under mild conditions. Moreover, this protocol was successfully applied to prepare structurally diverse nitrogen-containing frameworks.
Grafting of copper(II) Schiff base complex on functionalized multi-wall carbon nanotubes: Synthesis, characterization and catalytic aziridination of olefins
Bazarganipour, Mehdi,Salavati-Niasari, Masoud
, p. 57 - 64 (2015/06/30)
In this study, hydroxyl functionalized copper(II) Schiff-base; [Cu((OH)2-salophen)], [(OH)2-salophen] = (N,N-bis(4-hydroxysalicylidene) phenylene-1,2-diamine); has been covalently anchored on modified multi-wall carbon nanotubes (MWN