1. Açık Erişim@BUU
  2. İndeksli Yayınlar
  3. Web of Science
Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/33491
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dc.contributor.authorErdem, İhsan-
dc.contributor.authorGronert, Scott-
dc.contributor.authorCabrera, Gabriel-
dc.contributor.authorTapken, Marco-
dc.date.accessioned2023-08-15T06:54:37Z-
dc.date.available2023-08-15T06:54:37Z-
dc.date.issued2017-05-26-
dc.identifier.citationErden, İ. vd. (2017). ''Diverse Modes of Reactivity of 6-(Chloromethyl)-6-methylfulvene''. European Journal of Organic Chemistry, 20(2017), 2925-2931.en_US
dc.identifier.issn1434-193X-
dc.identifier.issn1099-0690-
dc.identifier.urihttps://doi.org/10.1002/ejoc.201700442-
dc.identifier.urihttps://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/ejoc.201700442-
dc.identifier.urihttp://hdl.handle.net/11452/33491-
dc.description.abstractThe title compound exhibits a number of modes of reactivity toward nucleophiles/bases owing to the presence of several electrophilic and potentially nucleophilic sites in the molecule. We explored the reactions of 6-(chloromethyl)-6-methylfulvene with oxygen and nitrogen nucleophiles and bases as well as a carbon-based nucleophile (an enamine) and realized all possible reactivity modes predicted on the basis of electrophilic and nucleophilic positions in this compound.en_US
dc.description.sponsorshipUnited States Department of Health & Human Services National Institutes of Health (NIH) - USA - SC1 GM082340en_US
dc.description.sponsorshipNational Science Foundation (NSF) - CHE-1565852 - CHE-1228656en_US
dc.description.sponsorshipUnited States Department of Health & Human Services National Institutes of Health (NIH) - USA - R25-GM059298 Appeared in source as:NIH MBRS-RISE scholarshipen_US
dc.description.sponsorshipNIH-MS-PhD Bridge scholarship - R-25-GM048972en_US
dc.description.sponsorshipNational Science Foundation (NSF) NSF - Directorate for Mathematical & Physical Sciences (MPS) - 1565852en_US
dc.language.isoenen_US
dc.publisherWiley-V C Hen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectChemistryen_US
dc.subjectFulvenesen_US
dc.subjectNucleophilic additionen_US
dc.subjectCycloadditionen_US
dc.subject1,2-Dihydropentaleneen_US
dc.subjectReaction mechanismsen_US
dc.subjectSubstituted fulvenesen_US
dc.subjectCyclopentadieneen_US
dc.subjectDimethylfulveneen_US
dc.subjectCycloadditionen_US
dc.subject6,6-dimethylfulveneen_US
dc.subjectEliminationen_US
dc.subjectPrecursorsen_US
dc.subjectProductsen_US
dc.subjectAcetoneen_US
dc.subjectSystemen_US
dc.titleDiverse Modes of Reactivity of 6-(Chloromethyl)-6-methylfulveneen_US
dc.typeArticleen_US
dc.identifier.wos000403678500007tr_TR
dc.identifier.scopus2-s2.0-85020045276tr_TR
dc.relation.tubitakBIDEP-2219tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Fen-Edebiyat Fakültesi/Kimya Bölümü.tr_TR
dc.identifier.startpage29525tr_TR
dc.identifier.endpage2931tr_TR
dc.identifier.volume20tr_TR
dc.identifier.issue2017tr_TR
dc.relation.journalEuropean Journal of Organic Chemistryen_US
dc.contributor.buuauthorCoşkun, Necdet-
dc.contributor.researcheridB-1200-2012tr_TR
dc.relation.collaborationYurt dışıtr_TR
dc.identifier.pubmed29200937tr_TR
dc.subject.wosChemistry, organicen_US
dc.indexed.wosSCIEen_US
dc.indexed.wosICen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubMeden_US
dc.wos.quartileQ2en_US
dc.contributor.scopusid7004177880tr_TR
dc.subject.scopusFulvene; Isomers; Cyclopropenoneen_US
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