102535-92-2Relevant academic research and scientific papers
Nucleophilic ring opening of aziridines with amines under catalyst- and solvent-free conditions
Huang, Yi-Yong,Lv, Zong-Chao,Yang, Xing,Wang, Zhao-Lei,Zou, Xiao-Xue,Zhao, Zhen-Ni,Chen, Fei
, p. 924 - 927 (2017)
The aza-addition of aziridines to obtain vicinal-diamines was achieved under catalyst- and solvent-free conditions for the first time. Various aryl, alkyl and meso-bicyclic aziridines with a Ts-protecting group were tolerated, and aromatic amine-nucleophi
Reactions with Aziridines, 38. On the Regioselectivity of the Nucleophilic Ring Opening of Activated 2-Phenylaziridines
Onistschenko, Andreas,Buchholz, Berthold,Stamm, Helmut
, p. 2678 - 2680 (2007/10/02)
The ring of 1-mesyl (1c) and 1-(phenylcarbamoyl)-2-phenylaziridine (1d) is opened between N and C-2 (benzylic effect) by some nucleophiles in high yields.
