Regioselective and diastereoselective dimethyldioxirane epoxidation of substituted norbornenes and hexamethyl Dewar benzene

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.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.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.secondary<Go to ISI>://000084947700024-
heal.identifier.secondaryhttps://docs.google.com/file/d/0BxfLht5wJUEIM2ZjMmRhNjAtY2EzZi00ODdjLWIyZWEtYzRiMzY1NzNjZTY2/edit?hl=en-
heal.journalNameTetrahedron Letten
heal.journalTypepeer reviewed-
heal.languageen-
heal.publicationDate2000-
heal.publisherPergamon-Elsevieren
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

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