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dc.contributor.authorAkulov, A. A.en
dc.contributor.authorVaraksin, M. V.en
dc.contributor.authorMampuys, P.en
dc.contributor.authorCharushin, V. N.en
dc.contributor.authorChupakhin, O. N.en
dc.contributor.authorMaes, B. U. W.en
dc.date.accessioned2021-08-31T15:07:48Z-
dc.date.available2021-08-31T15:07:48Z-
dc.date.issued2021-
dc.identifier.citationC(sp2)-H functionalization in non-aromatic azomethine-based heterocycles / A. A. Akulov, M. V. Varaksin, P. Mampuys, et al. — DOI 10.1039/d0ob01580f // Organic and Biomolecular Chemistry. — 2021. — Vol. 19. — Iss. 2. — P. 297-312.en
dc.identifier.issn14770520-
dc.identifier.otherFinal2
dc.identifier.otherAll Open Access, Hybrid Gold3
dc.identifier.otherhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85099739487&doi=10.1039%2fd0ob01580f&partnerID=40&md5=14c9881b953f7955444424fd46c8cffd
dc.identifier.otherhttps://pubs.rsc.org/en/content/articlepdf/2021/ob/d0ob01580fm
dc.identifier.urihttp://elar.urfu.ru/handle/10995/103143-
dc.description.abstractDirect C(sp2)-H functionalization of the endocyclic azomethine and aldonitrone moieties in non-aromatic azaheterocycles has established itself as a promising methodology over the last decade. Transition metal-catalyzed cross-coupling reactions, α-metalation-electrophile quenching protocols, and (metal-free) nucleophilic substitution of hydrogen reactions (SNH) are the major routes applied on cyclic imines and their derivatives. In this overview, we show the tangible progress made in this area during the period from 2008 to 2020. This journal is © The Royal Society of Chemistry.en
dc.description.sponsorshipThe research was financially supported by the Russian Science Foundation (Project No. 20-43-01004), a bilateral Russian Science Foundation (RSF) – Fund for Scientific Research Flanders (FWO) project, and the Francqui Foundation.en
dc.format.mimetypeapplication/pdfen
dc.language.isoenen
dc.publisherRoyal Society of Chemistryen
dc.relationinfo:eu-repo/grantAgreement/RSF//20-43-01004en
dc.rightsinfo:eu-repo/semantics/openAccessen
dc.sourceOrg. Biomol. Chem.2
dc.sourceOrganic and Biomolecular Chemistryen
dc.subjectTRANSITION METALSen
dc.subjectAZA-HETEROCYCLESen
dc.subjectCYCLIC IMINESen
dc.subjectELECTROPHILESen
dc.subjectFUNCTIONALIZATIONSen
dc.subjectHETEROCYCLESen
dc.subjectHYDROGEN REACTIONen
dc.subjectMETAL-CATALYZED CROSS-COUPLING REACTIONSen
dc.subjectNUCLEOPHILIC SUBSTITUTIONSen
dc.subjectCHEMICAL REACTIONSen
dc.subjectREVIEWen
dc.titleC(sp2)-H functionalization in non-aromatic azomethine-based heterocyclesen
dc.typeReviewen
dc.typeinfo:eu-repo/semantics/reviewen
dc.typeinfo:eu-repo/semantics/publishedVersionen
dc.identifier.rsi44991288-
dc.identifier.doi10.1039/d0ob01580f-
dc.identifier.scopus85099739487-
local.contributor.employeeAkulov, A.A., Department of Organic and Biomolecular Chemistry, Ural Federal University, 19 Mira Str., Ekaterinburg, 620002, Russian Federation
local.contributor.employeeVaraksin, M.V., Department of Organic and Biomolecular Chemistry, Ural Federal University, 19 Mira Str., Ekaterinburg, 620002, Russian Federation, Institute of Organic Synthesis, Ural Branch, Russian Academy of Sciences, 22 S. Kovalevskaya Str., Ekaterinburg, 620990, Russian Federation
local.contributor.employeeMampuys, P., Division of Organic Synthesis, Department of Chemistry, University of Antwerp, Groenenborgerlaan 171, Antwerp, B-2020, Belgium
local.contributor.employeeCharushin, V.N., Department of Organic and Biomolecular Chemistry, Ural Federal University, 19 Mira Str., Ekaterinburg, 620002, Russian Federation, Institute of Organic Synthesis, Ural Branch, Russian Academy of Sciences, 22 S. Kovalevskaya Str., Ekaterinburg, 620990, Russian Federation
local.contributor.employeeChupakhin, O.N., Department of Organic and Biomolecular Chemistry, Ural Federal University, 19 Mira Str., Ekaterinburg, 620002, Russian Federation, Institute of Organic Synthesis, Ural Branch, Russian Academy of Sciences, 22 S. Kovalevskaya Str., Ekaterinburg, 620990, Russian Federation
local.contributor.employeeMaes, B.U.W., Division of Organic Synthesis, Department of Chemistry, University of Antwerp, Groenenborgerlaan 171, Antwerp, B-2020, Belgium
local.description.firstpage297-
local.description.lastpage312-
local.issue2-
local.volume19-
dc.identifier.wos000609532200023-
local.contributor.departmentDepartment of Organic and Biomolecular Chemistry, Ural Federal University, 19 Mira Str., Ekaterinburg, 620002, Russian Federation
local.contributor.departmentInstitute of Organic Synthesis, Ural Branch, Russian Academy of Sciences, 22 S. Kovalevskaya Str., Ekaterinburg, 620990, Russian Federation
local.contributor.departmentDivision of Organic Synthesis, Department of Chemistry, University of Antwerp, Groenenborgerlaan 171, Antwerp, B-2020, Belgium
local.identifier.pure20893290-
local.identifier.pured7457d3c-445b-4e42-a856-cd03ef42620buuid
local.identifier.eid2-s2.0-85099739487-
local.fund.rsf20-43-01004-
local.identifier.wosWOS:000609532200023-
local.identifier.pmid33026389-
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