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Photochemical synthesis of chrysenols

dc.contributor.authorJørgensen, Kåre B.
dc.contributor.authorJoensen, Majbritt
dc.date.accessioned2009-10-27T12:29:08Z
dc.date.issued2008-08
dc.identifier.issn1563-5333
dc.identifier.issn1040-6638
dc.identifier.urihttp://hdl.handle.net/11250/182359
dc.description.abstractChrysenols are formed together with other metabolites when chrysene is metabolized in living organisms. The principal metabolites are needed as pure compounds for reference materials and standards to study various aspects of this metabolism. In this study the 1-, 2-, 3-, and 4-chrysenols have been made in pure form by photochemical ring closure of [(methoxyphenyl)vinyl]naphthalene to the methoxychrysenes followed by deprotection, and purification of the chrysenols. The method may be applied to make the single pure compounds in high yields.en
dc.format.extent57833 bytes
dc.format.mimetypeapplication/pdf
dc.language.isoengen
dc.publisherTaylor & Francisen
dc.rightsNavngivelse-Ikkekommersiell 4.0 Internasjonal
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/deed.no
dc.subjectPhotocyclizationen
dc.subjecthydroxychryseneen
dc.subjectchrysenolen
dc.subjectsynthesisen
dc.subjectmetabolitesen
dc.titlePhotochemical synthesis of chrysenolsen
dc.typePeer revieweden
dc.typeJournal articleen
dc.subject.nsiVDP::Mathematics and natural science: 400::Basic biosciences: 470::Biochemistry: 476en
dc.source.pagenumber362 - 372en
dc.source.volumeVol. 28en
dc.source.journalPolycyclic Aromatic Compoundsen
dc.source.issue4 & 5en
dc.identifier.doi10.1080/10406630802374580


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Navngivelse-Ikkekommersiell 4.0 Internasjonal
Except where otherwise noted, this item's license is described as Navngivelse-Ikkekommersiell 4.0 Internasjonal