Abstract:
Ring opening in aziridine tri- and tetramers with HBr leads to the stable hydrobromides of corresponding N1-(β-bromoethyl)-ethyleneamines; an initial mixture of linear and branched tetraethyleneimine isomers yielded only a linear bromo derivative.
Document Type:
Article
Language: English
Citation:
N. M. Nepomnyaschaya, E. A. Tsvetkova, Yu. A. Strelenko, “Oligoaziridines: ring opening with hydrobromic acid”, Mendeleev Commun., 14:2 (2004), 78–79
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