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dc.contributor.authorAbdul Kareem Hamad Ayfan, Rasim Farraj Muslim-
dc.contributor.authorNoor Sabah Noori-
dc.date.accessioned2023-01-15T12:18:02Z-
dc.date.available2023-01-15T12:18:02Z-
dc.date.issued2019-
dc.identifier.citation10en_US
dc.identifier.issn0974-3618-
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/9280-
dc.description.abstractThis research includes synthesis of new heterocyclic derivatives of novel disubstituted 1,3- oxazepine-tetra-onefrom Schiff bases reaction with 3-methylfuran-2,5-dione and 3-phenyldihydrofuran-2,5-dione. Schiff bases [A1-A5] were synthesized by the reaction of aromatic aldehydes with primary aromatic amines, in the presence ofglacial acetic acid as catalyst in absolute ethanol. The novel derivatives[A6-A10] were obtained from treatment ofSchiff bases with anhydrides. The synthesized compounds were identified by TLC and via spectral methods,their (FT-IR, 1H-NMR and 13C-NMR) and measurements of some of its physical propertieen_US
dc.language.isoen_USen_US
dc.publisherA and V Publications / Research Journal of Pharmacy and Technologyen_US
dc.subject1H-NMRen_US
dc.subject13C-NMRen_US
dc.subjectTLCen_US
dc.subjectSchiff basesen_US
dc.subjectoxazepine-tetra-one.en_US
dc.titlePreparation and characterization of novel disubstituted 1,3- oxazepine-tetra-one from schiff bases reaction with 3-methylfuran-2,5-dione and 3-phenyldihydrofuran-2,5-dioneen_US
dc.typeArticleen_US
Appears in Collections:كلية الصيدلة



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