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dc.contributor.authorParker, K. A.en
dc.contributor.authorFokas, D.en
dc.date.accessioned2015-11-24T17:38:32Z-
dc.date.available2015-11-24T17:38:32Z-
dc.identifier.issn0022-3263-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/14508-
dc.rightsDefault Licence-
dc.subjectmodified curtius reactionen
dc.subjectconvenient reagenten
dc.subjectorganic-synthesisen
dc.subjectreducing agenten
dc.subjecttris(trimethylsilyl)silaneen
dc.subject(-)-morphineen
dc.subjectreductionen
dc.subjectalkenesen
dc.subjectketonesen
dc.subjectestersen
dc.titleStereochemistry of Radical Cyclizations to Side-Chain Olefinic Bonds - an Approach to Control of the C-9 Center of Morphineen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.primaryDoi 10.1021/Jo00093a026-
heal.identifier.secondary<Go to ISI>://A1994NX38400026-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Μηχανικών Επιστήμης Υλικώνel
heal.publicationDate1994-
heal.abstractStyrenes of general structure 5 undergo tandem radical cyclization to cis,cis-hydrophenanthrofurans 9, products which contain the carbocyclic skeleton of the morphine alkaloids. Vinylurethane 5E-NHCO(2)Et cyclizes to 9 alpha via the intermediate radical 7E-NHCO(2)Et in the chair-chair conformation. Cyclization of 5Z-NHCO(2)Et also gives predominantly 9 alpha instead of the expected 9 beta. This anomaly is attributed to the isomerization of 5Z to 5E at a rate competitive with that of cyclization.en
heal.publisherAmerican Chemical Societyen
heal.journalNameJournal of Organic Chemistryen
heal.journalTypepeer reviewed-
heal.fullTextAvailabilityTRUE-
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά)

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