11-Hydroxy-3,3-dimethyl-7,12-dioxo-3,4,6,6a,7,12,12a,12b-octahydrobenz[a]anthracen-1-yl acetate

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dc.contributor.authorRozek, T.
dc.contributor.authorBowie, J.
dc.contributor.authorSkelton, B.
dc.contributor.authorWhite, A.
dc.date.issued2003
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.identifier.citationActa Crystallographica Section C: Crystal Structure Communications, 2003; 59(8):O431-O432
dc.identifier.doi10.1107/S0108270103013374
dc.identifier.issn0108-2701
dc.identifier.issn1600-5759
dc.identifier.urihttp://hdl.handle.net/2440/17944
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
pubs.publication-statusPublished

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