Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/17944
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dc.contributor.authorRozek, T.-
dc.contributor.authorBowie, J.-
dc.contributor.authorSkelton, B.-
dc.contributor.authorWhite, A.-
dc.date.issued2003-
dc.identifier.citationActa Crystallographica Section C: Crystal Structure Communications, 2003; 59(8):O431-O432-
dc.identifier.issn0108-2701-
dc.identifier.issn1600-5759-
dc.identifier.urihttp://hdl.handle.net/2440/17944-
dc.descriptionCopyright © International Union of Crystallography-
dc.description.abstractThe Diels-Alder reaction between 5-hydroxy-1,4-naphthoquinone and 5,5-dimethyl-3-vinyl-1,2-cyclohexadienyl acetate by endo addition gives the title compound, C(22)H(22)O(5), in 68% yield. This racemic diastereoisomer has the opposite regiochemistry to ochromycinone analogues produced previously and may allow access to a new type of anticancer-active saquayamycin analogue.-
dc.description.statementofresponsibilityTomas Rozek, John H. Bowie, Brian W. Skeltonb and Allan H. White-
dc.language.isoen-
dc.publisherMunksgaard Int Publ Ltd-
dc.source.urihttp://journals.iucr.org/c/issues/2003/08/00/ta1412/ta1412.pdf-
dc.title11-Hydroxy-3,3-dimethyl-7,12-dioxo-3,4,6,6a,7,12,12a,12b-octahydrobenz[a]anthracen-1-yl acetate-
dc.typeJournal article-
dc.identifier.doi10.1107/S0108270103013374-
pubs.publication-statusPublished-
Appears in Collections:Aurora harvest 6
Chemistry publications

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