Please use this identifier to cite or link to this item: https://olympias.lib.uoi.gr/jspui/handle/123456789/13911
Full metadata record
DC FieldValueLanguage
dc.contributor.authorParker, K. A.en
dc.contributor.authorFokas, D.en
dc.date.accessioned2015-11-24T17:33:55Z-
dc.date.available2015-11-24T17:33:55Z-
dc.identifier.issn0022-3263-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/13911-
dc.rightsDefault Licence-
dc.subjectlithium aluminum-hydrideen
dc.subjectasymmetric reductionen
dc.subjectradical cyclizationsen
dc.subjectkinetic resolutionen
dc.subjectformamidinesulfinic aciden
dc.subjectenantiomeric purityen
dc.subjectmorphine alkaloidsen
dc.subject5-exo cyclizationsen
dc.subjectaminyl radicalsen
dc.subjectcyclic-ketonesen
dc.titleEnantioselective synthesis of (-)-dihydrocodeinone: A short formal synthesis of (-)-morphineen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.primaryDoi 10.1021/Jo0513008-
heal.identifier.secondary<Go to ISI>://000234837500001-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Μηχανικών Επιστήμης Υλικώνel
heal.publicationDate2006-
heal.abstractThe radical cyclization approach to the morphine alkaloids has been applied in an asymmetric synthesis of (-)-dihydrocodeinone. A chiral cyclohexenol (R-32), from the CBS reduction of the enone, is the source of chirality. The first key step, tandem closure in which stereochemistry is controlled by geometric constraints, (-)-15b -> (+)-16, was followed by an unprecedented reductive hydroamination, completing the synthesis of (-)-dihydroisocodeine ((-)-17) in 13 steps from commercially available materials.en
heal.publisherAmerican Chemical Societyen
heal.journalNameJournal of Organic Chemistryen
heal.journalTypepeer reviewed-
heal.fullTextAvailabilityTRUE-
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά)

Files in This Item:
File Description SizeFormat 
Fokas-2006-Ena.pdf330.96 kBAdobe PDFView/Open    Request a copy


This item is licensed under a Creative Commons License Creative Commons