Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12258/2962
Title: Electrophilically activated nitroalkanes in the synthesis of 6,7-dihydro-1H-cyclopenta[g]perimidines
Authors: Aksenov, A. V.
Аксенов, А. В.
Aksenov, N. A.
Аксенов, Н. А.
Ovcharov, D. S.
Овчаров, Д. С.
Shcherbakov, S. V.
Щербаков, С. В.
Smirnova, A. N.
Смирнова, А. Н.
Aksenova, I. V.
Аксенова, И. В.
Goncharov, V. I.
Гончаров, В. И.
Rubin, M. A.
Рубин, М. А.
Keywords: Thin-film transistors;Channel organic semiconductors;Perylene bisimides;Acenes;Photovoltaics;Acetamination;Performance;Derivatives;Electronics;Perimidines
Issue Date: 2017
Publisher: Maik Nauka Publishing / Springer SBM
Citation: Aksenov, A.V., Aksenov, N.A., Ovcharov, D.S., Shcherbakov, S.V., Smirnova, A.N., Aksenova, I.V., Goncharov, V.I., Rubin, M.A. Electrophilically activated nitroalkanes in the synthesis of 6,7-dihydro-1H-cyclopenta[g]perimidines // Russian Journal of Organic Chemistry. - 2017. - Volume 53. - Issue 7. - Pages 1081-1084
Series/Report no.: Russian Journal of Organic Chemistry
Abstract: A highly efficient synthetic route to 6,7-dihydro-1H-cyclopenta[gh]perimidines has been proposed on the basis of a novel reaction of nitroalkanes with 4,5-diaminoacenaphthene in the presence of polyphosphoric acid. The reaction involves phosphorylation of the aci-nitro compound, followed by intramolecular cyclization
URI: https://www.scopus.com/record/display.uri?eid=2-s2.0-85028604314&origin=resultslist&sort=plf-f&src=s&nlo=1&nlr=20&nls=afprfnm-t&affilName=north+caucasus+federal+university&sid=0a0f0434fb9e513c7f0fb58254b47a91&sot=afnl&sdt=sisr&sl=53&s=%28AF-ID%28%22North+Caucasus+Federal+University%22+60070541%29%29&ref=%28Electrophilically+activated+nitroalkanes+in+the+synthesis+of+6%2c7-dihydro-1H-cyclopenta%5bg%5dperimidines%29&relpos=1&citeCnt=1&searchTerm=
http://hdl.handle.net/20.500.12258/2962
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