Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12258/10138
Title: Electrophilically activated nitroalkanes in reaction with aliphatic diamines en route to imidazolines
Authors: Aksenov, A. V.
Аксенов, А. В.
Aksenov, N. A.
Аксенов, Н. А.
Arutiunov, N. A.
Арутюнов, Н. А.
Malyuga, V. V.
Малюга, В. В.
Ovcharov, S. N.
Овчаров, С. Н.
Rubin, M. A.
Рубин, М. А.
Keywords: Amines;Aliphatic diamines;Aromatic amines;Benzimidazoles;En-route;Imidazolines;Nitroalkanes;Phosphorous acid;Synthetic methodology;Paraffins
Issue Date: 2019
Publisher: Royal Society of Chemistry
Citation: Aksenov, A.V., Aksenov, N.A., Arutiunov, N.A., Malyuga, V.V., Ovcharov, S.N., Rubin, M. Electrophilically activated nitroalkanes in reaction with aliphatic diamines en route to imidazolines // RSC Advances. - 2019. - Volume 9. - Issue 67. - Pages 39458-39465
Series/Report no.: RSC Advances
Abstract: A novel synthetic methodology for the assembly of imidazolines via an unusual reaction between nitroalkanes and aliphatic 1,2-diamines in the presence of phosphorous acid is described. In contrast to the related highly efficient preparation of benzimidazoles from aromatic amines, this process represents a major synthetic challenge and for a long time was elusive. Analysis of the method limitations is provided
URI: https://www.scopus.com/record/display.uri?eid=2-s2.0-85076163416&origin=resultslist&sort=plf-f&src=s&st1=Electrophilically+activated+nitroalkanes+in+reaction+with+aliphatic+diamines+en+route+to+imidazolines&st2=&sid=d26f2c404dd20f2650d6d115a369a105&sot=b&sdt=b&sl=116&s=TITLE-ABS-KEY%28Electrophilically+activated+nitroalkanes+in+reaction+with+aliphatic+diamines+en+route+to+imidazolines%29&relpos=0&citeCnt=0&searchTerm=
http://hdl.handle.net/20.500.12258/10138
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