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dc.contributor.authorCobb, J.en
dc.contributor.authorDemetropoulos, I. N.en
dc.contributor.authorKorakas, D.en
dc.contributor.authorSkoulika, S.en
dc.contributor.authorVarvounis, G.en
dc.date.accessioned2015-11-24T16:49:05Z-
dc.date.available2015-11-24T16:49:05Z-
dc.identifier.issn0040-4020-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/9425-
dc.rightsDefault Licence-
dc.titleSynthesis and reactions of 1-aryl-2-nitropyrroles. Structural and conformational study of ethyl N-[2'-[1'-(2-nitropyrrolyl)]phenyl]-N-toluene-4-sulfonamide glycinateen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.primaryDoi 10.1016/0040-4020(96)00096-8-
heal.identifier.secondary<Go to ISI>://A1996UA51000029-
heal.identifier.secondaryhttp://ac.els-cdn.com/0040402096000968/1-s2.0-0040402096000968-main.pdf?_tid=ab16a622-34ac-11e3-abf0-00000aab0f01&acdnat=1381740376_c14e9a89c38ed8aab5e3c921ffd8b210-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.publicationDate1996-
heal.abstractNitration of 1-aryl(or 1-benzyl)pyrroles 1, 2 and 7 has provided the corresponding 2- and 3-nitropyrroles 3 and 5, 4 and 6, and 8 and 9 in a 1:2 ratio. Reductive cyclisation of 3 and 8, gave pyrrolo[1,2-a]quinazolines 11 and 12. and pyrrolo[1,2-b][2,4]benzodiazepine 13. respectively. A conformational study of 5 in the solid and Liquid state using X-ray diffraction analysis. molecular dynamics calculations and NMR spectroscopy is described.en
heal.publisherElsevieren
heal.journalNameTetrahedronen
heal.journalTypepeer reviewed-
heal.fullTextAvailabilityTRUE-
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά). ΧΗΜ

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