Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/9280
Title: Preparation 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-dione
Authors: Abdul Kareem Hamad Ayfan, Rasim Farraj Muslim
Noor Sabah Noori
Keywords: 1H-NMR
13C-NMR
TLC
Schiff bases
oxazepine-tetra-one.
Issue Date: 2019
Publisher: A and V Publications / Research Journal of Pharmacy and Technology
Citation: 10
Abstract: This 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 propertie
URI: http://localhost:8080/xmlui/handle/123456789/9280
ISSN: 0974-3618
Appears in Collections:كلية الصيدلة



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