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dc.contributor.authorTuyun, AMAÇ FATİH
dc.date.accessioned2021-03-03T07:35:23Z
dc.date.available2021-03-03T07:35:23Z
dc.date.issued2014
dc.identifier.citationTuyun A. F. , "Synthetic exploitation of halogenated alkenes containing an electron-withdrawing group: synthesis of alpha-chlorohydrazones and ketene aminals by regiospecific reactions of in situ generated imide chlorides", TETRAHEDRON LETTERS, cilt.55, sa.13, ss.2085-2089, 2014
dc.identifier.issn0040-4039
dc.identifier.otherav_12bf906c-c750-4297-9a84-93fcac816562
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/18054
dc.identifier.urihttps://doi.org/10.1016/j.tetlet.2014.02.038
dc.description.abstractA concise approach for the construction of ketene aminals and alpha-chlorohydrazones has been developed. It involves reactions of the regiodefined gem-dihalo nitrovinyl compound of in situ generated imide chlorides in different media with primary arylamines being dependent on the aryl groups. A range of ketene aminals and alpha-chlorohydrazones are obtained in good to high yields. In addition, alpha-aminohydrazones are prepared by using alpha-chlorohydrazones as the precursors. (C) 2014 Elsevier Ltd. All rights reserved.
dc.language.isoeng
dc.subjectTemel Bilimler (SCI)
dc.subjectBiyoinorganik Kimya
dc.subjectKİMYA, ORGANİK
dc.subjectKimya
dc.subjectBiyokimya
dc.subjectTemel Bilimler
dc.titleSynthetic exploitation of halogenated alkenes containing an electron-withdrawing group: synthesis of alpha-chlorohydrazones and ketene aminals by regiospecific reactions of in situ generated imide chlorides
dc.typeMakale
dc.relation.journalTETRAHEDRON LETTERS
dc.contributor.departmentBeykent Üniversitesi , Mühendislik-Mimarlık Fakültesi , Kimya Mühendisliği
dc.identifier.volume55
dc.identifier.issue13
dc.identifier.startpage2085
dc.identifier.endpage2089
dc.contributor.firstauthorID718528


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