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https://dspace.ncfu.ru/handle/20.500.12258/2962
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DC Field | Value | Language |
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dc.contributor.author | Aksenov, A. V. | - |
dc.contributor.author | Аксенов, А. В. | - |
dc.contributor.author | Aksenov, N. A. | - |
dc.contributor.author | Аксенов, Н. А. | - |
dc.contributor.author | Ovcharov, D. S. | - |
dc.contributor.author | Овчаров, Д. С. | - |
dc.contributor.author | Shcherbakov, S. V. | - |
dc.contributor.author | Щербаков, С. В. | - |
dc.contributor.author | Smirnova, A. N. | - |
dc.contributor.author | Смирнова, А. Н. | - |
dc.contributor.author | Aksenova, I. V. | - |
dc.contributor.author | Аксенова, И. В. | - |
dc.contributor.author | Goncharov, V. I. | - |
dc.contributor.author | Гончаров, В. И. | - |
dc.contributor.author | Rubin, M. A. | - |
dc.contributor.author | Рубин, М. А. | - |
dc.date.accessioned | 2018-09-13T09:47:16Z | - |
dc.date.available | 2018-09-13T09:47:16Z | - |
dc.date.issued | 2017 | - |
dc.identifier.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 | ru |
dc.identifier.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= | - |
dc.identifier.uri | http://hdl.handle.net/20.500.12258/2962 | - |
dc.description.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 | ru |
dc.language.iso | en | ru |
dc.publisher | Maik Nauka Publishing / Springer SBM | ru |
dc.relation.ispartofseries | Russian Journal of Organic Chemistry | - |
dc.subject | Thin-film transistors | ru |
dc.subject | Channel organic semiconductors | ru |
dc.subject | Perylene bisimides | ru |
dc.subject | Acenes | ru |
dc.subject | Photovoltaics | ru |
dc.subject | Acetamination | ru |
dc.subject | Performance | ru |
dc.subject | Derivatives | ru |
dc.subject | Electronics | ru |
dc.subject | Perimidines | ru |
dc.title | Electrophilically activated nitroalkanes in the synthesis of 6,7-dihydro-1H-cyclopenta[g]perimidines | ru |
dc.type | Статья | ru |
vkr.amount | Pages 1081-1084 | ru |
vkr.inst | Институт математики и естественных наук | - |
Appears in Collections: | Статьи, проиндексированные в SCOPUS, WOS |
Files in This Item:
File | Description | Size | Format | |
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scopusresults 254 .pdf Restricted Access | 62.23 kB | Adobe PDF | View/Open | |
WoS 135 .pdf Restricted Access | 243.84 kB | Adobe PDF | View/Open |
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