Please use this identifier to cite or link to this item: https://olympias.lib.uoi.gr/jspui/handle/123456789/9052
Full metadata record
DC FieldValueLanguage
dc.contributor.authorAsouti, A.en
dc.contributor.authorHadjiarapoglou, L. P.en
dc.date.accessioned2015-11-24T16:46:16Z-
dc.date.available2015-11-24T16:46:16Z-
dc.identifier.issn0040-4039-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/9052-
dc.rightsDefault Licence-
dc.subjectdimethyldioxiraneen
dc.subjectepoxidationen
dc.subjectdiastereoselectivityen
dc.subjectregioselectivityen
dc.subjectsubstituted norbornenesen
dc.subjectcatalytic asymmetric epoxidationen
dc.subjectketone catalystsen
dc.subjectdioxiranesen
dc.subjectchemistryen
dc.subjectoxidationen
dc.subjectolefinsen
dc.subjectdesignen
dc.titleRegioselective and diastereoselective dimethyldioxirane epoxidation of substituted norbornenes and hexamethyl Dewar benzeneen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.secondary<Go to ISI>://000084947700024-
heal.identifier.secondaryhttps://docs.google.com/file/d/0BxfLht5wJUEIM2ZjMmRhNjAtY2EzZi00ODdjLWIyZWEtYzRiMzY1NzNjZTY2/edit?hl=en-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.publicationDate2000-
heal.abstractVarious substituted norbornenes, such as endo-dicyclopentadiene 1, exo-dicyclopentadiene 5, 5-methylenebicyclo[2.2.1]hept-2-ene 8 and hexamethyl Dewar benzene 10 were transformed into the corresponding mono- and bis-epoxides by epoxidation with dimethyldioxirane (as an acetone solution). (C) 2000 Elsevier Science Ltd. All rights reserved.en
heal.publisherPergamon-Elsevieren
heal.journalNameTetrahedron Letten
heal.journalTypepeer reviewed-
heal.fullTextAvailabilityTRUE-
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά). ΧΗΜ

Files in This Item:
File Description SizeFormat 
Hadjiarapoglou-2000-Regioselective and diastereoselective.pdf115.6 kBAdobe PDFView/Open    Request a copy


This item is licensed under a Creative Commons License Creative Commons