Please use this identifier to cite or link to this item: http://dspace.uniten.edu.my/jspui/handle/123456789/9744
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dc.contributor.authorAlhadi, A.A.
dc.contributor.authorOthman, R.
dc.contributor.authorYehye, W.A.
dc.contributor.authorRahman, N.A.
dc.date.accessioned2018-03-06T03:49:19Z-
dc.date.available2018-03-06T03:49:19Z-
dc.date.issued2015
dc.identifier.urihttp://dspace.uniten.edu.my/jspui/handle/123456789/9744-
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.
dc.titleFormation of 1,3,4-oxadiazolines and 1,3,4-oxadiazepines through acetylation of salicylic hydrazones
item.grantfulltextnone-
item.fulltextNo Fulltext-
crisitem.author.deptUniversiti Tenaga Nasional-
Appears in Collections:COE Scholarly Publication
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