Please use this identifier to cite or link to this item: https://repository.cihe.edu.hk/jspui/handle/cihe/1517
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dc.contributor.authorBligh, Annie Sim Wanen_US
dc.contributor.otherMachakanur, S. S.-
dc.contributor.otherPatil, B. R.-
dc.contributor.otherBadiger, D. S.-
dc.contributor.otherPathan, A. H.-
dc.contributor.otherGudasi, K. B.-
dc.date.accessioned2021-10-15T11:23:15Z-
dc.date.available2021-10-15T11:23:15Z-
dc.date.issued2012-
dc.identifier.urihttps://repository.cihe.edu.hk/jspui/handle/cihe/1517-
dc.description.abstractA series of novel symmetric triazine hydrazones [N<sub>3</sub>C<sub>3</sub>(-OC<sub>6</sub>H<sub>4</sub>-p-C(CH<sub>3</sub>)=N-NH-C(O)-C<sub>6</sub>H<sub>4</sub>-p-X)<sub>3</sub>] (X = H, Br, Cl, F, OH, OCH<sub>3</sub>, CH<sub>3</sub>, NO<sub>2</sub>, NH<sub>2</sub>) were prepared in excellent yields by a three-fold condensation reaction of 2,4,6- tris(4-acetylphenoxy)-1,3,5-triazine with p-substituted benzoic acid hydrazides [NH<sub>2</sub>-NH-C(O)-C<sub>6</sub>H<sub>4</sub>-p-X]. The structures were confirmed by FT-IR, <sup>1</sup>H, <sup>13</sup>C, 2D-HMQC NMR and mass spectrometry (MALDI-TOF).en_US
dc.language.isoenen_US
dc.publisherBentham Scienceen_US
dc.relation.ispartofLetters in Organic Chemistryen_US
dc.titleSynthesis of novel tri-arm star shaped 1,3,5-triazine hydrazones from 2,4,6-tris(4-acetylphenoxy)-1,3,5-triazine coreen_US
dc.typejournal articleen_US
dc.identifier.doi10.2174/157017812799304051-
dc.contributor.affiliationSchool of Health Sciencesen_US
dc.relation.issn1875-6255en_US
dc.description.volume9en_US
dc.description.issue1en_US
dc.description.startpage29en_US
dc.description.endpage34en_US
dc.cihe.affiliatedNo-
item.fulltextWith Fulltext-
item.grantfulltextopen-
item.openairecristypehttp://purl.org/coar/resource_type/c_6501-
item.cerifentitytypePublications-
item.openairetypejournal article-
item.languageiso639-1en-
crisitem.author.deptS.K. Yee School of Health Sciences-
crisitem.author.orcid0000-0002-4757-2159-
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