Hydrated forms of N-[(3R)-3-(4-methyl-3,5-dioxo-1,2,4-triazolidin-1-yl)-2-methylene-butanoyl]-(1S,2R)-bornane-10,2-sultam and its enantiomer

dc.contributor.authorElemes, Y.en
dc.contributor.authorMuir, K. W.en
dc.date.accessioned2015-11-24T16:39:11Z
dc.date.available2015-11-24T16:39:11Z
dc.identifier.issn0108-2701-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/8127
dc.rightsDefault Licence-
dc.subjecttriazolinedione ene reactionsen
dc.subjectsinglet oxygenen
dc.subjectstereochemistryen
dc.subjectnitrosoareneen
dc.subjectderivativesen
dc.subjectaciden
dc.titleHydrated forms of N-[(3R)-3-(4-methyl-3,5-dioxo-1,2,4-triazolidin-1-yl)-2-methylene-butanoyl]-(1S,2R)-bornane-10,2-sultam and its enantiomeren
heal.abstractTriazolidinediones react with each enantiomeric bornanesultam derivative of tiglic acid to produce the appropriate ene adduct in high yield and with excellent regioselectivity and diastereoselectivity. The optically pure products, viz. N-[(3R)-3-(4methyl-3,5-dioxo-1,2,4-triazolidin-1-yl)-2-methylenebutanoyl](1S,2R)-bornane-10,2-sultam 0.15-hydrate, C(18)H(26)N(4)O(5)S(.)0.35H(2)O, and its enantiomer N-[(3S)-3-(4-methyl-3,5-dioxo1,2,4-triazolidin-1-yl)-2-methylenebutanoyl]-(1R,2S)-bornane10,2-sultam0.35-hydrate, C(18)H(26)N(4)O(5)S(.)0.35H(2)O, have been characterized by spectroscopy and single- crystal X- ray analysis. Their structures are the result of C ss-re attack of the enophile on the double bond of the alkene.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.primaryDoi 10.1107/S0108270106019524-
heal.identifier.secondary<Go to ISI>://000239485400024-
heal.identifier.secondaryhttp://journals.iucr.org/c/issues/2006/08/00/dn3017/dn3017.pdf-
heal.journalNameActa Crystallographica Section C-Crystal Structure Communicationsen
heal.journalTypepeer reviewed-
heal.languageen-
heal.publicationDate2006-
heal.publisherInternational Union of Crystallographyen
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

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