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dc.contributor.authorAsouti, A.en
dc.contributor.authorHadjiarapoglou, L. P.en
dc.date.accessioned2015-11-24T16:45:44Z-
dc.date.available2015-11-24T16:45:44Z-
dc.identifier.issn0040-4039-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/8976-
dc.rightsDefault Licence-
dc.subjectiodonium ylideen
dc.subject[3+2]-cycloadditionen
dc.subjectdihydrofuranen
dc.subjectiodonium ylidesen
dc.subjectdipolar cycloadditionen
dc.subjectcarbenoid reactionsen
dc.subjectorganic-synthesisen
dc.subjectdecompositionen
dc.subjectdiazocarbonylen
dc.subjectcyclizationen
dc.title[3+2]-cycloaddition reactions of 2-phenyliodonio-1,3-dioxacyclohexanemethylide: Facile synthesis of fused dihydrofuran derivativesen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.secondary<Go to ISI>://000077080000040-
heal.identifier.secondaryhttp://ac.els-cdn.com/S0040403998019972/1-s2.0-S0040403998019972-main.pdf?_tid=ba7b47bf00b6bebf635c7b841bf5c51d&acdnat=1333030005_fbab2254174ad83bd456b828f267c9f6-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.publicationDate1998-
heal.abstractIodonium ylide 2, derived from 1,3-cyclohexadione, undergoes thermal [3+2]-cycloaddition with acetonirile, carbon disulfide and p, P'- dimethoxythiobenzophenone with Cu(acac)(2) catalysis to form the corresponding 5-membered heterocycles and alkene respectively. Photochemically 2 reacts with various alkenes and dienes to form dihydrofuran derivatives, key intermediates for paniculide A, B and pentalene synthesis. (C) 1998 Elsevier Science Ltd. All rights reserved.en
heal.journalNameTetrahedron Letten
heal.journalTypepeer reviewed-
heal.fullTextAvailabilityTRUE-
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά). ΧΗΜ

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