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dc.contributor.authorShaikh, A. K.en
dc.contributor.authorCobb, A. J. A.en
dc.contributor.authorVarvounis, G.en
dc.date.accessioned2015-11-24T16:41:52Z-
dc.date.available2015-11-24T16:41:52Z-
dc.identifier.issn1523-7060-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/8482-
dc.rightsDefault Licence-
dc.subjecto-quinone methidesen
dc.subjectdiels-alder reactionsen
dc.subjectaqueous-solutionen
dc.subjectbiomimetic synthesisen
dc.subjectefficient methoden
dc.subjectcross-linkingen
dc.subjectderivativesen
dc.subjecttautomerizationen
dc.subjectphotogenerationen
dc.subject(+/-)-alboatrinen
dc.titleMild and Rapid Method for the Generation of ortho-(Naphtho)quinone Methide Intermediatesen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.primaryDoi 10.1021/Ol203196n-
heal.identifier.secondary<Go to ISI>://000299238600041-
heal.identifier.secondaryhttp://pubs.acs.org/doi/pdfplus/10.1021/ol203196n-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.publicationDate2012-
heal.abstractA new mild method has been devised for generating o-(naphtho)quinone methides via fluoride-induced desilylation of silyl derivatives of o-hydroxybenzyl(or 1-naphthylmethyl) nitrate. The reactive o-(naphtho)quinone methide intermediates were trapped by C, O, N, and S nucleophiles and underwent "inverse electron-demand" hetero-Diels-Alder reaction with dienophiles to give stable adducts. The method has useful potential application in natural product synthesis and drug research.en
heal.publisherAmerican Chemical Societyen
heal.journalNameOrg Letten
heal.journalTypepeer reviewed-
heal.fullTextAvailabilityTRUE-
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά). ΧΗΜ

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