Please use this identifier to cite or link to this item:
https://hdl.handle.net/2440/17944
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Full metadata record
DC Field | Value | Language |
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dc.contributor.author | Rozek, T. | - |
dc.contributor.author | Bowie, J. | - |
dc.contributor.author | Skelton, B. | - |
dc.contributor.author | White, A. | - |
dc.date.issued | 2003 | - |
dc.identifier.citation | Acta Crystallographica Section C: Crystal Structure Communications, 2003; 59(8):O431-O432 | - |
dc.identifier.issn | 0108-2701 | - |
dc.identifier.issn | 1600-5759 | - |
dc.identifier.uri | http://hdl.handle.net/2440/17944 | - |
dc.description | Copyright © International Union of Crystallography | - |
dc.description.abstract | The 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.statementofresponsibility | Tomas Rozek, John H. Bowie, Brian W. Skeltonb and Allan H. White | - |
dc.language.iso | en | - |
dc.publisher | Munksgaard Int Publ Ltd | - |
dc.source.uri | http://journals.iucr.org/c/issues/2003/08/00/ta1412/ta1412.pdf | - |
dc.title | 11-Hydroxy-3,3-dimethyl-7,12-dioxo-3,4,6,6a,7,12,12a,12b-octahydrobenz[a]anthracen-1-yl acetate | - |
dc.type | Journal article | - |
dc.identifier.doi | 10.1107/S0108270103013374 | - |
pubs.publication-status | Published | - |
Appears in Collections: | Aurora harvest 6 Chemistry publications |
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