Electrophilically activated nitroalkanes in the synthesis of 6,7-dihydro-1H-cyclopenta[g]perimidines

Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/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:	http://hdl.handle.net/20.500.12258/2962
Appears in Collections:	Статьи, проиндексированные в SCOPUS, WOS

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