Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12258/3722
Title: Benzimidazoles and benzoxazoles via the nucleophilic addition of anilines to nitroalkanes
Authors: Aksenov, A. V.
Аксенов, А. В.
Smirnov, A. N.
Смирнов, А. Н.
Aksenov, N. A.
Аксенов, Н. А.
Bijieva, A. S.
Биджиева, А. С.
Aksenova, I. V.
Аксенова, И. В.
Rubin, M. A.
Рубин, М. А.
Keywords: Addition reaction;Aniline;Benzimidazole;Benzoxazoles;Cyclocondensation;Nitroalkanes;Nucleophilic addition;Umpolung
Issue Date: 2015
Publisher: Royal Society of Chemistry
Citation: Aksenov, A.V., Smirnov, A.N., Aksenov, N.A., Bijieva, A.S., Aksenova, I.V., Rubin, M. Benzimidazoles and benzoxazoles via the nucleophilic addition of anilines to nitroalkanes // Organic and Biomolecular Chemistry. - 2015. - Volume 13. - Issue 14. - Pages 4289-4295
Series/Report no.: Organic and Biomolecular Chemistry
Abstract: PPA-induced umpolung triggers efficient nucleophilic addition of unactivated anilines to nitroalkanes to produce N-hydroxyimidamides. The latter undergo sequential acid-promoted cyclocondensation with ortho-OH or ortho-NHR moieties to afford benzoxazoles and benzimidazoles, respectively
URI: https://www.scopus.com/record/display.uri?eid=2-s2.0-84925835134&origin=resultslist&sort=plf-f&src=s&nlo=1&nlr=20&nls=afprfnm-t&affilName=north+caucasus+federal+university&sid=fe656e0c7517dbc25228b3d577bd000c&sot=afnl&sdt=cl&cluster=scopubyr%2c%222015%22%2ct&sl=53&s=%28AF-ID%28%22North+Caucasus+Federal+University%22+60070541%29%29&relpos=35&citeCnt=19&searchTerm=
http://hdl.handle.net/20.500.12258/3722
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