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Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/86029
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dc.contributor.authorRussell, R.A.-
dc.contributor.authorCollin, G.J.-
dc.contributor.authorGee, P.S.-
dc.contributor.authorWarrener, R.N.-
dc.date.issued1983-
dc.identifier.citationJournal of the Chemical Society, Chemical Communications, 1983; 1983(18):994-995-
dc.identifier.issn0022-4936-
dc.identifier.urihttp://hdl.handle.net/2440/86029-
dc.description.abstract5,8-Diacetoxy-2-acetyl-3,4-dihydronaphthalene, prepared by a new route from the Diels–Alder adduct of buta-1,3-diene and p-benzoquinone, is selectively deacetylated (Cs2CO3 in tetrahydrofuran or K2CO3 in dimethyl sulphoxide) to intermediates suitable for use in chiral anthracycline synthesis.-
dc.description.statementofresponsibilityRichard A. Russell, Geoffrey J. Collin, Paul S. Gee and Ronald N. Warrener-
dc.language.isoen-
dc.publisherRoyal Society of Chemistry-
dc.rightsCopyright status unknown-
dc.source.urihttp://dx.doi.org/10.1039/c39830000994-
dc.titleAn economical and versatile synthesis of 5,8-dialkoxy-2-acetyl-3,4-dihydronaphthalenes: key precursors for the synthesis of chiral anthracyclines-
dc.typeJournal article-
dc.identifier.doi10.1039/c39830000994-
pubs.publication-statusPublished-
Appears in Collections:Aurora harvest 7
Chemistry publications

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