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dc.contributor.authorErfle, Silke-
dc.contributor.authorLanger, Peter-
dc.date.accessioned2021-03-10T08:30:37Z-
dc.date.available2021-03-10T08:30:37Z-
dc.date.issued2020-
dc.identifier.issn2525-2321-
dc.identifier.urihttps://dspace.ctu.edu.vn/jspui/handle/123456789/46271-
dc.description.abstractThe reaction of dimethyl 3,5-dioxopimelate, a readily available 1,3,5,7-tetracarbonyl compound, with benzyne resulted in formation of a highly functionalized naphthalene derivative which is formed by an unprecedentcd domino ‘insertion / aldol condensation’ reaction.vi_VN
dc.language.isovivi_VN
dc.relation.ispartofseriesVietnam Journal of Chemistry;No.06, Vol.58 .- P.841-843-
dc.subjectNaphthalenevi_VN
dc.subjectBenzynevi_VN
dc.subjectInsertionsvi_VN
dc.subject1,3-dicarbonyl compoundsvi_VN
dc.subjectDoinino reactionvi_VN
dc.titleDomino Reaction of Benzyne with Dimethyl 3,5-Dioxopimelatevi_VN
dc.typeArticlevi_VN
Appears in Collections:Vietnam Journal of Chemistry

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