Please use this identifier to cite or link to this item: http://dspace2020.uniten.edu.my:8080/handle/123456789/3508
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dc.contributor.authorWateh, A.N.-
dc.contributor.authorThy, C.K.-
dc.contributor.authorChee, C.F.-
dc.contributor.authorRahman, N.A.-
dc.date.accessioned2017-10-27T06:14:30Z-
dc.date.available2017-10-27T06:14:30Z-
dc.date.issued2015-
dc.identifier.urihttp://dspace.uniten.edu.my:80/jspui/handle/123456789/3508-
dc.description.abstractAn efficient synthesis of (±)-cycloillicinone was accomplished in five steps from sesamol. The title compound was obtained via a biomimetic Diels-Alder cycloaddition between illicinone A and β-trans-ocimene as the key step. © 2015 Taylor and Francis Group, LLC.-
dc.language.isoen-
dc.relation.ispartofSynthetic Communications Volume 45, Issue 16, 18 August 2015, Pages 1920-1927-
dc.titleAn efficient synthesis of (±)-cycloillicinone-
dc.typeArticle-
dc.identifier.doi10.1080/00397911.2015.1022833-
item.cerifentitytypePublications-
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.openairetypeArticle-
crisitem.author.deptUniversiti Tenaga Nasional-
Appears in Collections:COE Scholarly Publication
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