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Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/85911
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dc.contributor.authorWarrener, R.N.-
dc.contributor.authorGee, P.S.-
dc.contributor.authorRussell, R.A.-
dc.date.issued1981-
dc.identifier.citationJournal of the Chemical Society, Chemical Communications, 1981; 1981(21):1100-1101-
dc.identifier.issn0022-4936-
dc.identifier.urihttp://hdl.handle.net/2440/85911-
dc.description.abstractThe (–)-(R)-dienone (13) was prepared in 10 steps from the known 8-hydroxy-5-methoxy-2, 3-dihydronaphthalen-1(4H)-one (2), and the chirality at C(7) in (13) corresponds to that found at C(9) in the naturally occurring anthracyclines related to daunomycin.-
dc.description.statementofresponsibilityRonald N. Warrener, Paul S. Gee and Richard A. Russell-
dc.language.isoen-
dc.publisherRoyal Society of Chemistry-
dc.rightsCopyright status unknown-
dc.source.urihttp://dx.doi.org/10.1039/c39810001100-
dc.titlePreparation of (–)-(7R)-7-acetyl-7-hydroxy-4,4-dimethoxy-5,6,7,8-tetrahydro-naphthalen-1(4H)-one, a chiral AB-synthon for anthracycline synthesis-
dc.typeJournal article-
dc.identifier.doi10.1039/c39810001100-
pubs.publication-statusPublished-
Appears in Collections:Aurora harvest 7
Chemistry publications

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