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dc.contributor.authorMaha Saleh Mahdi, Abdullah Hussein Kshash-
dc.date.accessioned2022-10-25T10:51:46Z-
dc.date.available2022-10-25T10:51:46Z-
dc.date.issued2020-
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/6495-
dc.description.abstractNew derivatives of 1,3-oxazepine(1b–7b)(1c–7c) were synthesized by the reaction of Schiff bases (1a–7a) with Succinicand Maleic anhydrideusing dry benzene as a solvent. Schiff bases (1a–7a)were prepared by condensation of 4,4'- Diaminodiphenylmethanewith methoxy and halobenzaldehydeusing absolute ethanol as a solvent in the presence of glacial acetic acid as a catalyst. All synthesized compounds were monitored by TLC and characterized using spectroscopy techniques such as (FT-IR), (1H-NMR) and (13C-NMR), they revealed that all synthesized compounds were conformity of the proposed structures.en_US
dc.publisherBiochem. Cell. Archen_US
dc.subjectSchiff basesen_US
dc.subjectoxazepineen_US
dc.subjectsuccinic anhydrideen_US
dc.subjectmaleic anhydrideen_US
dc.titleSYNTHESIS AND CHARACTERIZATION OF TWO MOIETIES OF-1,3- OXAZEPINE-1,5-DIONE COMPOUNDS VIA 4,4'- DIAMINODIPHENYLMETHANE IMINES AS PRECURSORSen_US
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