Please use this identifier to cite or link to this item: https://dspace.ctu.edu.vn/jspui/handle/123456789/109439
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dc.contributor.authorRevayat, Sattar-
dc.contributor.authorMehranpour, Abdolmohammad-
dc.date.accessioned2024-12-21T13:47:13Z-
dc.date.available2024-12-21T13:47:13Z-
dc.date.issued2024-
dc.identifier.issn2525-2321-
dc.identifier.urihttps://dspace.ctu.edu.vn/jspui/handle/123456789/109439-
dc.description.abstractIn this article, four different stable benzaminium salts were synthesized from the one-pot reaction of oxyacetic acid with aminothiophenol or aminophenol derivatives under Vilsmeier- Haack conditions in the presence of triethylamine in acetonitrile at reflux. The structure of the new compounds was confirmed based on their spectral data from ¹H NMR and ¹³C NMR and elemental analysis.vi_VN
dc.language.isoenvi_VN
dc.relation.ispartofseriesVietnam journal of Chemitry;Vol.62, Iss.05 .- P.634-637-
dc.subjectBenzenaminium saltsvi_VN
dc.subjectCyanine dyesvi_VN
dc.subjectOxyacetic acidvi_VN
dc.subjectOxytrimethinium saltsvi_VN
dc.subjectSynthesisvi_VN
dc.titleSynthesis of new stable benzenaminium salts using oxyacetic acid derivatives via oxytrimethinium salts as intermediatesvi_VN
dc.typeArticlevi_VN
Appears in Collections:Vietnam Journal of Chemistry

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