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Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/47583
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dc.contributor.authorMacreadie, I.-
dc.contributor.authorAvery, T.-
dc.contributor.authorRobinson, A.-
dc.contributor.authorMacreadie, P.-
dc.contributor.authorBarraclough, M.-
dc.contributor.authorTaylor, D.-
dc.contributor.authorTiekink, E.-
dc.date.issued2008-
dc.identifier.citationTetrahedron: the international journal for the rapid publication of full original research papers and critical reviews in organic chemistr, 2008; 64(7):1225-1232-
dc.identifier.issn0040-4020-
dc.identifier.urihttp://hdl.handle.net/2440/47583-
dc.descriptionCopyright © 2007 Elsevier Ltd All rights reserved.-
dc.description.abstractIn an ongoing effort to rationally design new antimicrobials, 47 new 1,2-dioxines have been synthesised. Broad antifungal structure–activity relationships governing aromatically substituted epoxy-1,2-dioxines 2 and 3 and their parent 1,2-dioxines 1 were assessed primarily against the pathogenic yeast, Candida albicans, with haemolytic activity of selected examples also reported.-
dc.description.urihttp://www.elsevier.com/wps/find/journaldescription.cws_home/942/description#description-
dc.language.isoen-
dc.publisherPergamon-Elsevier Science Ltd-
dc.source.urihttp://dx.doi.org/10.1016/j.tet.2007.11.071-
dc.titleDesign of 1,2-dioxines with anti-Candida activity: aromatic substituted 1,2-dioxines-
dc.typeJournal article-
dc.identifier.doi10.1016/j.tet.2007.11.071-
pubs.publication-statusPublished-
dc.identifier.orcidAvery, T. [0000-0001-6882-5461]-
dc.identifier.orcidTaylor, D. [0000-0002-3302-4610] [0000-0002-4274-3983] [0000-0003-0633-7424]-
Appears in Collections:Aurora harvest
Chemistry publications

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