Dimethyldioxirane Epoxidation of 6,6-Disubstituted Fulvenes

dc.contributor.authorAdam, W.en
dc.contributor.authorHadjiarapoglou, L.en
dc.contributor.authorMeffert, A.en
dc.date.accessioned2015-11-24T16:56:17Z
dc.date.available2015-11-24T16:56:17Z
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/10411
dc.rightsDefault Licence-
dc.titleDimethyldioxirane Epoxidation of 6,6-Disubstituted Fulvenesen
heal.abstractThe endocyclic bis-epoxides of various pentafulvenes were readily prepared by epoxidation with excess dimethyldioxirane; stoichiometric epoxidation yielded mixtures of the bis-epoxides and the labile mono-epoxides, but no exocyclic epoxides were observed.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.secondaryhttp://www.sciencedirect.com/science/article/pii/S0040403900935780-
heal.journalNameTetrahedron Letten
heal.journalTypepeer reviewed-
heal.languageen-
heal.publicationDate1991-
heal.publisherElsevieren
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

Αρχεία

Φάκελος/Πακέτο αδειών

Προβολή: 1 - 1 of 1
Φόρτωση...
Μικρογραφία εικόνας
Ονομα:
license.txt
Μέγεθος:
1.74 KB
Μορφότυπο:
Item-specific license agreed upon to submission
Περιγραφή: