N. M. Nepomnyaschaya, E. A. Tsvetkova, Yu. A. Strelenko, “Oligoaziridines: ring opening with hydrobromic acid”, Mendeleev Commun., 14:2 (2004), 78

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Mendeleev Communications, 2004, Volume 14, Issue 2, Pages 78–79
DOI: https://doi.org/10.1070/MC2004v014n02ABEH001871 (Mi mendc3815)

Oligoaziridines: ring opening with hydrobromic acid

N. M. Nepomnyaschaya, E. A. Tsvetkova, Yu. A. Strelenko

N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation

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DOI: https://doi.org/10.1070/MC2004v014n02ABEH001871

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.

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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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https://www.mathnet.ru/eng/mendc/v14/i2/p78

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