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Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/85866
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dc.contributor.authorRussell, R.A.-
dc.contributor.authorWarrener, R.N.-
dc.date.issued1981-
dc.identifier.citationJournal of the Chemical Society, Chemical Communications, 1981; 1981(3):108-110-
dc.identifier.issn0022-4936-
dc.identifier.urihttp://hdl.handle.net/2440/85866-
dc.description.abstractA direct, versatile, one-step synthesis of anthraquinones which exhibits total regioselectivity (>99%) and involves the reaction of the anion of 4- or 7-methoxy-3-phenylsulphonylphthalides with variously substituted quinone monoacetals is reported.-
dc.description.statementofresponsibilityRichard A. Russell and Ronald N. Warrener-
dc.language.isoen-
dc.publisherRoyal Society of Chemistry-
dc.rightsCopyright status unknown-
dc.source.urihttp://dx.doi.org/10.1039/c39810000108-
dc.titleThe regiospecific preparation of 1,4-dioxygenated anthraquinones: a new route to islandicin, digitopurpone, and madeirin-
dc.typeJournal article-
dc.identifier.doi10.1039/c39810000108-
pubs.publication-statusPublished-
Appears in Collections:Aurora harvest 7
Chemistry publications

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