Please use this identifier to cite or link to this item: http://148.72.244.84/xmlui/handle/xmlui/5113
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dc.contributor.authorReem.S.Najem-
dc.date.accessioned2023-10-19T09:57:27Z-
dc.date.available2023-10-19T09:57:27Z-
dc.date.issued2015-
dc.identifier.issn2222-8373-
dc.identifier.urihttp://148.72.244.84:8080/xmlui/handle/xmlui/5113-
dc.description.abstractThe thiosemicarbazid was reacted with carbon disulfide .the result of their reaction was 5- amino 1,3,4 thiadiazol [1] .then the resulted compound was retreated with acetic anhydride to optain 5- mercapto 1,3,4 thiadiazol-2-yl acetamaied [2] to synthese 5 amino 1,3.4 thiadiazole-2- thiol [3]. This compound was allowed to react with aromatic aldehyde in precense of sodium hydroxide the resulted of the reaction -5- (2- amino-4-methyl thio1,3,4 thiadiazol (2H) yl -6- (1,3) oxazine 1,3 thiazine(4-6)(7-12)through reaction with urea and thio urea .the chemical structures of the products were characterized by (FT-IR) and (1H-NMR) (10,11) and melting points apparatus.en_US
dc.description.sponsorshiphttps://djps.uodiyala.edu.iq/en_US
dc.language.isoenen_US
dc.publisherUniversity of Diyalaen_US
dc.subject5-2amino -4- 5- methyl thio 1,3,4 thaidiazol -3- (2H) yl 1,3 thiazine 1,3 oxazine , Antibacterial .)en_US
dc.titleSynthesis and biological activity evalution of some new 1,3 – oxazine and 1,3 –thiazinederivedfrom (5-amino-1,3,4-thiadiazole- 2-thiol).en_US
dc.typeArticleen_US
Appears in Collections:مجلة ديالى للعلوم الاكاديمية / Academic Science Journal (Acad. Sci. J.)

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