DBU-Mediated Dimerization: Facile Access to 9,9′-Bifluorenylidenes and Isoindigos

dc.contributor.authorPurahong N.
dc.contributor.authorHongthong S.
dc.contributor.authorChotsaeng N.
dc.contributor.authorKuhakarn C.
dc.contributor.authorMeesin J.
dc.contributor.otherMahidol University
dc.date.accessioned2023-09-15T18:01:18Z
dc.date.available2023-09-15T18:01:18Z
dc.date.issued2023-01-01
dc.description.abstractThe present work describes 1,8-diazabicyclo[5.4.0]-7-undecene (DBU)-promoted self-dimerization of 9-chlorofluorenes and 3-chlorooxindoles for the production of the respective 9,9′-bifluorenylidene and isoindigo derivatives in moderate to good yields (29-97% yield). The reaction readily proceeded under mild and metal-free conditions with short reaction time. A scale-up synthesis (5.0 mmol) of some selected 9,9′-bifluorenylidene derivatives in decent yields highlights the synthetic utility of the reported protocol.
dc.identifier.citationSynlett (2023)
dc.identifier.doi10.1055/a-2158-7980
dc.identifier.eissn14372096
dc.identifier.issn09365214
dc.identifier.scopus2-s2.0-85169894504
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/90014
dc.rights.holderSCOPUS
dc.subjectChemistry
dc.titleDBU-Mediated Dimerization: Facile Access to 9,9′-Bifluorenylidenes and Isoindigos
dc.typeArticle
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85169894504&origin=inward
oaire.citation.titleSynlett
oairecerif.author.affiliationRajabhat Rajanagarindra University
oairecerif.author.affiliationKing Mongkut's Institute of Technology Ladkrabang
oairecerif.author.affiliationMahidol University

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