An economical and versatile synthesis of 5,8-dialkoxy-2-acetyl-3,4-dihydronaphthalenes: key precursors for the synthesis of chiral anthracyclines

Simple item page
dc.contributor.authorRussell, R.A.
dc.contributor.authorCollin, G.J.
dc.contributor.authorGee, P.S.
dc.contributor.authorWarrener, R.N.
dc.date.issued1983
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.identifier.citationJournal of the Chemical Society, Chemical Communications, 1983; 1983(18):994-995
dc.identifier.doi10.1039/c39830000994
dc.identifier.issn0022-4936
dc.identifier.urihttp://hdl.handle.net/2440/86029
dc.language.isoen
dc.publisherRoyal Society of Chemistry
dc.rightsCopyright status unknown
dc.source.urihttps://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
pubs.publication-statusPublished

Files

Collections

Chemistry publications