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BielawskiChristopher W

Bielawski, Christopher W.
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DC Field Value Language
dc.citation.endPage 5125 -
dc.citation.number 29 -
dc.citation.startPage 5123 -
dc.citation.title TETRAHEDRON LETTERS -
dc.citation.volume 47 -
dc.contributor.author Boydston, Andrew J. -
dc.contributor.author Khramov, Dimitri M. -
dc.contributor.author Bielawski, Christopher W. -
dc.date.accessioned 2023-12-22T09:44:33Z -
dc.date.available 2023-12-22T09:44:33Z -
dc.date.created 2020-07-13 -
dc.date.issued 2006-07 -
dc.description.abstract Cyclization of N-aryl and N-alkyl 2,5-diamino-1,4-benzoquinonediimines using paraformaldehyde under acidic conditions followed by oxidation with catalytic amounts of Pd(OAc)(2) afforded their respective benzobis(imidazolium) salts in yields of 48-98%. A comparative solid-state study between a 2,5-diamino-1,4-benzoquinonediimine and its corresponding benzobis(imidazolium) dichloride was also performed. -
dc.identifier.bibliographicCitation TETRAHEDRON LETTERS, v.47, no.29, pp.5123 - 5125 -
dc.identifier.doi 10.1016/j.tetlet.2006.05.076 -
dc.identifier.issn 0040-4039 -
dc.identifier.scopusid 2-s2.0-33744976128 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/33055 -
dc.identifier.url https://www.sciencedirect.com/science/article/pii/S0040403906010008?via%3Dihub -
dc.identifier.wosid 000238697600029 -
dc.language 영어 -
dc.publisher PERGAMON-ELSEVIER SCIENCE LTD -
dc.title An alternative synthesis of benzobis(imidazolium) salts via a 'one-pot' cyclization/oxidation reaction sequence -
dc.type Article -
dc.description.isOpenAccess FALSE -
dc.relation.journalWebOfScienceCategory Chemistry, Organic -
dc.relation.journalResearchArea Chemistry -
dc.type.docType Article -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.subject.keywordPlus CARBENE -
dc.subject.keywordPlus COMPLEXES -
dc.subject.keywordPlus DERIVATIVES -
dc.subject.keywordPlus AZOPHENINE -
dc.subject.keywordPlus POLYMERS -
dc.subject.keywordPlus QUINONE -

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