Please use this identifier to cite or link to this item: http://37.48.73.109:8080/jspui/jspui/handle/123456789/1401
Full metadata record
DC FieldValueLanguage
dc.contributor.authorAHMED N. AYYASH-
dc.date.accessioned2020-01-09T17:50:45Z-
dc.date.available2020-01-09T17:50:45Z-
dc.date.issued2013-
dc.identifier.issn2319-4014-
dc.identifier.urihttp://37.48.73.109:8080/jspui/jspui/handle/123456789/1401-
dc.description.abstractThe one-step polar nucleophilic (2+5=7) polar cycloaddition reaction of phthalimide with Schiff bases derived from heterocyclic amines and heterocyclic aldehydes or ketones in dry tetrahydrofuran (THF) gave 1H-2,3-disubstituted- [1,2-e][1,3]-benzodiazepine-4,7-dionesin good yields. The products were identified by their melting points, UV, FT-IR and 1HNMR spectra.en_US
dc.publisherInternational Journal of Applieden_US
dc.subjectBenzodiazepine-4, 7-Dione, Phthalimide, Schiff Bases, Synthesisen_US
dc.titleSYNTHESIS AND CHARACTERIZATION OF NEW DERIVATIVES OF 1H-2, 3- DISUBSTITUTED-[1, 2-e] [1, 3]-BENZODIAZEPINE-4, 7-DIONEen_US
Appears in Collections:البحوث العلمية

Files in This Item:
File Description SizeFormat 
IASET 1.pdf436.69 kBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.