The regiospecific preparation of 1,4-dioxygenated anthraquinones: a new route to islandicin, digitopurpone, and madeirin

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dc.contributor.authorRussell, R.A.
dc.contributor.authorWarrener, R.N.
dc.date.issued1981
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.identifier.citationJournal of the Chemical Society, Chemical Communications, 1981; 1981(3):108-110
dc.identifier.doi10.1039/c39810000108
dc.identifier.issn0022-4936
dc.identifier.urihttp://hdl.handle.net/2440/85866
dc.language.isoen
dc.publisherRoyal Society of Chemistry
dc.rightsCopyright status unknown
dc.source.urihttps://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
pubs.publication-statusPublished

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