1374142-50-3Relevant 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
supporting information, p. 924 - 927 (2017/08/18)
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
Efficient and regioselective ring-opening of arylaziridines with alcohols, thiols, amines and N-heteroaromatic compounds using sulphated zirconia
Llaveria, Josep,Espinoza, Araceli,Negrón, Guillermo,Isabel Matheu,Castillón, Sergio
supporting information; experimental part, p. 2525 - 2529 (2012/06/18)
Sulphated zirconia is an efficient catalyst for the regioselective ring-opening of aryl-substituted aziridines. This heterogeneous catalyst can be used several times without loss of activity and is compatible with a variety of acid sensitive and slightly basic nucleophiles.
