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Cycloaddition reactions of some tricyclic imides

dc.contributor.authorKulu I.
dc.contributor.authorGul M.
dc.contributor.authorGunkara O.T.
dc.contributor.authorOcal N.
dc.date.accessioned2019-09-01T12:50:17Z
dc.date.available2019-09-01T12:50:17Z
dc.date.issued2013
dc.identifier.issn1570193X
dc.identifier.urihttps://dx.doi.org/10.2174/1570193X113106660017
dc.identifier.urihttps://hdl.handle.net/20.500.12450/646
dc.description.abstractOur research group has published numerous papers over the last three years on the reaction of nitrile oxides and azomethine ylide with unsaturated tricyclic N-substituted dicarboximides selected according to the importance of possible biological activities. These reactions cover full range of mechanistic pathways and timings of bond-forming processes to give five-membered ring closure by 1,3-dipolar cycloaddition. © 2013 Bentham Science Publishers.en_US
dc.language.isoengen_US
dc.relation.isversionof10.2174/1570193X113106660017en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subject1,3-dipolar cycloadditionen_US
dc.subjectAzomethine ylideen_US
dc.subjectBiological active moleculesen_US
dc.subjectHydrazonesen_US
dc.subjectIsoxazolinesen_US
dc.subjectNitrile oxidesen_US
dc.subjectTricyclic imidesen_US
dc.titleCycloaddition reactions of some tricyclic imidesen_US
dc.typearticleen_US
dc.relation.journalMini-Reviews in Organic Chemistryen_US
dc.identifier.volume10en_US
dc.identifier.issue4en_US
dc.identifier.startpage409en_US
dc.identifier.endpage418en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.contributor.department-tempKulu, I., Yildiz Technical University, Davutpasa Campus, 34220 Istanbul, Turkey -- Gul, M., University of Amasya, 05100, Amasya, Turkey -- Gunkara, O.T., Yildiz Technical University, Davutpasa Campus, 34220 Istanbul, Turkey -- Ocal, N., Yildiz Technical University, Davutpasa Campus, 34220 Istanbul, Turkeyen_US


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