SYNTHETIC EXPLOITATION OF HALOGENATED ALKENES CONTAINING ELECTRON-WITHDRAWING GROUP (EWG): ACCESS TO VALUABLE 2,4-DINITROTHIOPHENES VIA RING-CLOSING AND RING-OPENING/RING-CLOSING PROTOCOLS

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dc.contributor.authorTuyun, Amac Fatih
dc.date.accessioned2024-03-13T10:33:17Z
dc.date.available2024-03-13T10:33:17Z
dc.date.issued2013
dc.departmentİstanbul Beykent Üniversitesien_US
dc.description.abstractWith the goal of their exploitation for the synthesis of highly functionalized 2,4-dinitrothiophenes, 2-(2,3-dichloro-1,3-dinitroallylidene)-1,3-dithiolane (2), derived from the initial ring-closing of polyhalogenated nitrobutadienic building blocks with 1,2-ethanedithiol, were reacted with secondary amines. After protic work up, highly functionalized 2,4-dinitrothiophenes have been accomplished via ring-opening/ring-closing protocols.en_US
dc.identifier.doi10.3987/COM-13-12860
dc.identifier.endpage2598en_US
dc.identifier.issn0385-5414
dc.identifier.issn1881-0942
dc.identifier.issue12en_US
dc.identifier.scopus2-s2.0-84889249005en_US
dc.identifier.scopusqualityQ4en_US
dc.identifier.startpage2589en_US
dc.identifier.urihttps://doi.org/10.3987/COM-13-12860
dc.identifier.urihttps://hdl.handle.net/20.500.12662/3869
dc.identifier.volume87en_US
dc.identifier.wosWOS:000330487600009en_US
dc.identifier.wosqualityQ3en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.language.isoenen_US
dc.publisherPergamon-Elsevier Science Ltden_US
dc.relation.ispartofHeterocyclesen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectThiopheneen_US
dc.subjectNitrothiopheneen_US
dc.subjectDithiolaneen_US
dc.subjectButa-1,3-dieneen_US
dc.subjectNitrobutadienyl Blocken_US
dc.titleSYNTHETIC EXPLOITATION OF HALOGENATED ALKENES CONTAINING ELECTRON-WITHDRAWING GROUP (EWG): ACCESS TO VALUABLE 2,4-DINITROTHIOPHENES VIA RING-CLOSING AND RING-OPENING/RING-CLOSING PROTOCOLSen_US
dc.typeArticleen_US

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