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dc.contributor.authorIrgashev, R. A.en
dc.contributor.authorKazin, N. A.en
dc.contributor.authorRusinov, G. L.en
dc.contributor.authorCharushin, V. N.en
dc.date.accessioned2019-07-22T06:43:48Z-
dc.date.available2019-07-22T06:43:48Z-
dc.date.issued2018-
dc.identifier.citationAn improved protocol for the preparation of 5, 11-dialkyl-6, 12-di(hetero)aryl-5, 11-dihydroindolo[3, 2-b]carbazoles and synthesis of their new 2, 8-dicyano-/2, 8-bis(benzo[d]thiazol-2-yl)-substituted derivatives / R. A. Irgashev, N. A. Kazin, G. L. Rusinov et al. // Arkivoc. — 2018. — Vol. 2018. — Iss. 5. — P. 203-220.en
dc.identifier.issn1551-7004-
dc.identifier.otherhttps://www.arkat-usa.org/get-file/63822/pdf
dc.identifier.other1good_DOI
dc.identifier.other6fa13088-e707-469b-874a-f1c856600aedpure_uuid
dc.identifier.otherhttp://www.scopus.com/inward/record.url?partnerID=8YFLogxK&scp=85052661508m
dc.identifier.urihttp://elar.urfu.ru/handle/10995/75071-
dc.description.abstractA number of 5, 11-dialkyl-6, 12-di(hetero)aryl-5, 11-dyhydroindolo[3, 2-b]carbazoles has been synthesized by modified method based on HBr catalyzed condensation of (hetero)aromatic aldehydes with indole in MeCN solution affording 5, 6, 11, 12-tetrahydroindolo[3, 2-b]carbazoles, that have been aromatized with I2 in DMF solution for 1 h at reflux, followed by alkylation of 5, 11-dihydro compounds. New 2, 8-dicyano-(10 examples) as well as 2, 8-bis(benzo[d]thiazol-2-yl)-substituted (5 examples) derivatives of these 5, 11-dyhydroindolo[3, 2-b]carbazoles have been obtained through their initial C2, 8-formylation, followed by treatment of dialdehydes with excess of hydroxylamine and dehydration of the formed aldoximes with acetic anhydride or by interaction with excess of 2-aminothiophenol in DMSO solution, respectively. © 2018 Arkat. All rights reserved.en
dc.description.sponsorshipThis research study was supported financially by the Russian Science Foundation (Project No. 16-13-10435).en
dc.format.mimetypeapplication/pdfen
dc.language.isoenen
dc.publisherArkaten
dc.relationinfo:eu-repo/grantAgreement/RSF//16-13-10435en
dc.rightsinfo:eu-repo/semantics/openAccessen
dc.sourceArkivocen
dc.subjectALDEHYDESen
dc.subjectBENZO[D]THIAZOLESen
dc.subjectINDOLEen
dc.subjectINDOLO[3,2-B]CARBAZOLEen
dc.subjectN-HETEROACENESen
dc.subjectNITRILESen
dc.titleAn improved protocol for the preparation of 5, 11-dialkyl-6, 12-di(hetero)aryl-5, 11-dihydroindolo[3, 2-b]carbazoles and synthesis of their new 2, 8-dicyano-/2, 8-bis(benzo[d]thiazol-2-yl)-substituted derivativesen
dc.typeArticleen
dc.typeinfo:eu-repo/semantics/articleen
dc.typeinfo:eu-repo/semantics/publishedVersionen
dc.identifier.rsi35773985-
dc.identifier.doi10.24820/ark.5550190.p010.557-
dc.identifier.scopus85052661508-
local.affiliationPostovsky Institute of Organic Synthesis, Ural Division of the Russian Academy of Sciences, Ekaterinburg, 620990, Russian Federationen
local.affiliationUral Federal University Named after the First President of Russia, B. N. Yeltsin, Ekaterinburg, 620002, Russian Federationen
local.contributor.employeeИргашев Роман Ахметовичru
local.contributor.employeeКазин Никита Андреевичru
local.contributor.employeeРусинов Геннадий Леонидовичru
local.contributor.employeeЧарушин Валерий Николаевичru
local.description.firstpage203-
local.description.lastpage220-
local.issue5-
local.volume2018-
dc.identifier.wos000456008800019-
local.identifier.pure7770887-
local.identifier.eid2-s2.0-85052661508-
local.fund.rsf16-13-10435-
local.identifier.wosWOS:000456008800019-
Располагается в коллекциях:Научные публикации ученых УрФУ, проиндексированные в SCOPUS и WoS CC

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