Curcuminoid–BF2 complexes: Synthesis, fluorescence and optimization of BF2 group cleavage

dc.bibliographicCitation.firstPage2264eng
dc.bibliographicCitation.journalTitleBeilstein Journal of Organic Chemistryeng
dc.bibliographicCitation.volume13eng
dc.contributor.authorWeiß, Henning
dc.contributor.authorReichel, Jeannine
dc.contributor.authorGörls, Helmar
dc.contributor.authorSchneider, Kilian R.A.
dc.contributor.authorMicheel, Mathias
dc.contributor.authorPröhl, Michael
dc.contributor.authorGottschaldt, Michael
dc.contributor.authorDietzek, Benjamin
dc.contributor.authorWeigand, Wolfgang
dc.date.accessioned2019-12-19T10:53:39Z
dc.date.available2019-12-19T10:53:39Z
dc.date.issued2017
dc.description.abstractEight difluoroboron complexes of curcumin derivatives carrying alkyne groups containing substituents have been synthesized following an optimised reaction pathway. The complexes were received in yields up to 98% and high purities. Their properties as fluorescent dyes have been investigated. Furthermore, a strategy for the hydrolysis of the BF2 group has been established using aqueous methanol and sodium hydroxide or triethylamine.eng
dc.description.versionpublishedVersioneng
dc.identifier.urihttps://doi.org/10.34657/5127
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/4711
dc.language.isoengeng
dc.publisherFrankfurt a.M. : Beilstein-Instituteng
dc.relation.doihttps://doi.org/10.3762/bjoc.13.223
dc.rights.licenseCC BY 4.0 Unportedeng
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/eng
dc.subject.ddc540eng
dc.subject.ddc620eng
dc.subject.otherBF2 complexeng
dc.subject.othercurcumineng
dc.subject.otherdyeseng
dc.subject.otherfluorescenceeng
dc.subject.otherhydrolysiseng
dc.subject.otherspectroscopyeng
dc.titleCurcuminoid–BF2 complexes: Synthesis, fluorescence and optimization of BF2 group cleavageeng
dc.typeArticleeng
dc.typeTexteng
tib.accessRightsopenAccesseng
wgl.contributorIPHTeng
wgl.subjectIngenieurwissenschafteneng
wgl.typeZeitschriftenartikeleng
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