Regiospecific synthesis of bis(quinone monoacetals) and their annelation to give bisanthraquinones

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dc.contributor.authorRussell, R.A.
dc.contributor.authorDay, A.I.
dc.contributor.authorPilley, B.A.
dc.contributor.authorLeavy, P.J.
dc.contributor.authorWarrener, R.N.
dc.date.issued1987
dc.description.abstractThe anodic oxidation of bis-(p-methoxyphenol) derivatives bearing methoxymethyl, methoxyethoxymethyl, or t-butyldimethylsilyl protecting groups affords regiospecifically bis-dienones which can be annelated with anions derived from 3-cyanophthalides to yield bisanthraquinones and bisanthracyclinones.
dc.description.statementofresponsibilityRichard A. Russell, Anthony I. Day, Boyd A. Pilley, Peter J. Leavy and Ronald N. Warrener
dc.identifier.citationJournal of the Chemical Society, Chemical Communications, 1987; 1987(21):1631-1633
dc.identifier.doi10.1039/c39870001631
dc.identifier.issn0022-4936
dc.identifier.urihttp://hdl.handle.net/2440/85937
dc.language.isoen
dc.publisherRoyal Society of Chemistry
dc.rightsCopyright status unknown
dc.source.urihttps://doi.org/10.1039/c39870001631
dc.titleRegiospecific synthesis of bis(quinone monoacetals) and their annelation to give bisanthraquinones
dc.typeJournal article
pubs.publication-statusPublished

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