Ferrocene as a Leaving Group; Unexpected Rearrangement Reactions for the Synthesis of 2,3-Diarylnapthoquinones

dc.contributor.author Kivrak, Arif
dc.contributor.author Ertas, Nevroz Aslan
dc.date.accessioned 2025-05-10T17:17:06Z
dc.date.available 2025-05-10T17:17:06Z
dc.date.issued 2020
dc.department T.C. Van Yüzüncü Yıl Üniversitesi en_US
dc.department-temp Van Yüzüncü Yil Üni̇versi̇tesi̇,Van Yüzüncü Yil Üni̇versi̇tesi̇ en_US
dc.description.abstract In general, Suzuki-Miyaura coupling reaction between aryl bromide and arylboronic acids formthe new C-C bond in the presence of Pd-catalyst. In the present study, 2-bromo-3-ferrocenyl1,4-naphthoquinone 2 intermediate is synthesized by starting from 2,3-dibromo-1,4-naphthoquinone via Suzuki-Miyaura Coupling reaction. Then, it is investigated that the reactionbetween 2 and arylboronic acids give a new rearrangement reaction involving free radicals.Ferrocene structure displays critical roles for the formation of 2,3-diaryl-1,4-naphthoquinones.This reaction could be first example for the radical C-C bond cleavage reactions includingferrocene. en_US
dc.identifier.endpage 27 en_US
dc.identifier.issn 1694-7398
dc.identifier.issue 1 en_US
dc.identifier.scopusquality N/A
dc.identifier.startpage 22 en_US
dc.identifier.trdizinid 358605
dc.identifier.uri https://search.trdizin.gov.tr/en/yayin/detay/358605/ferrocene-as-a-leaving-group-unexpected-rearrangement-reactions-for-the-synthesis-of-23-diarylnapthoquinones
dc.identifier.uri https://hdl.handle.net/20.500.14720/9125
dc.identifier.volume 8 en_US
dc.identifier.wosquality N/A
dc.language.iso en en_US
dc.relation.ispartof Manas Journal of Engineering en_US
dc.relation.publicationcategory Makale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanı en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject Kimya en_US
dc.subject Organik en_US
dc.title Ferrocene as a Leaving Group; Unexpected Rearrangement Reactions for the Synthesis of 2,3-Diarylnapthoquinones en_US
dc.type Article en_US
dspace.entity.type Publication

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