Please use this identifier to cite or link to this item: http://dspace.uniten.edu.my/jspui/handle/123456789/3513
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dc.contributor.authorAlhadi, A.A.en_US
dc.contributor.authorOthman, R.en_US
dc.contributor.authorYehye, W.A.en_US
dc.contributor.authorRahman, N.A.en_US
dc.date.accessioned2017-10-27T06:55:17Z-
dc.date.available2017-10-27T06:55:17Z-
dc.date.issued2015-
dc.description.abstractA new series of 1,3,4-oxadiazolines and 1,3,4-oxadiazepines are prepared in a one-step reaction through cyclization of various N-benzylidene-2-hydroxybenzohydrazides. Cyclization in acetic anhydride yielded 1,3,4-oxadiazolines, while the reaction carried out in acetic anhydride-acetic acid gave 1,3,4-oxadiazepines, in some cases. © 2014 Elsevier Ltd. All rights reserved.en_US
dc.language.isoenen_US
dc.relation.ispartofTetrahedron Letters Volume 56, Issue 4, 21 January 2015, Pages 573-576en_US
dc.titleFormation of 1,3,4-oxadiazolines and 1,3,4-oxadiazepines through acetylation of salicylic hydrazonesen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.tetlet.2014.12.037-
item.fulltextWith Fulltext-
item.grantfulltextopen-
crisitem.author.deptUniversiti Tenaga Nasional-
Appears in Collections:COE Scholarly Publication
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