Substrate-induced diastereoselectivity in the dimethyldioxirane epoxidation of simple alkenes and dienes

dc.contributor.authorAsouti, A.en
dc.contributor.authorHadjiarapoglou, L. P.en
dc.date.accessioned2015-11-24T16:48:45Z
dc.date.available2015-11-24T16:48:45Z
dc.identifier.issn0936-5214-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/9360
dc.rightsDefault Licence-
dc.subjectdimethyldioxiraneen
dc.subjectepoxidationen
dc.subjectdiasteroselectivityen
dc.subjectregioselectivityen
dc.subjecthydrogen-peroxideen
dc.subjecttransition-stateen
dc.subjectnatural producten
dc.subjectoxygen-transferen
dc.subjectdioxiranesen
dc.subjectoxidationen
dc.subjectchemistryen
dc.subjectethersen
dc.subjectmethyl(trifluoromethyl)dioxiraneen
dc.subject(+)-pramanicinen
dc.titleSubstrate-induced diastereoselectivity in the dimethyldioxirane epoxidation of simple alkenes and dienesen
heal.abstractVarious alkenes and dienes, such as (R)- or (S)-limonene 2, 2-carene 6, 3-carene 8, (R)-alpha -pinene 10, (S)-alpha -pinene 12, and endo-dicyclopentadiene 14 were transformed into the corresponding mono- and bis-epoxides by epoxidation with dimethyldioxirane (as an acetone solution). The selectivity observed in these epoxidations is explained by the assumption of hydrogen bonding between bridge protons and the dioxirane.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.secondary<Go to ISI>://000172596400006-
heal.identifier.secondaryhttps://docs.google.com/file/d/0BxfLht5wJUEIMzIyZDQ0ZWItNmYxOS00ZTkwLThlZTktZmMzNDk5ZDNmOWYy/edit?pli=1&hl=en-
heal.journalNameSynletten
heal.journalTypepeer reviewed-
heal.languageen-
heal.publicationDate2001-
heal.publisherGeorg Thieme Verlagen
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

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