Cycloaddition routes to polycyclic quinones: Part 1 boron triacetate as a regiochemical directing agent

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dc.contributor.authorRussell, R.A.
dc.contributor.authorCollin, G.J.
dc.contributor.authorSterns, M.
dc.contributor.authorWarrener, R.N.
dc.date.issued1979
dc.description.abstract9-Hydroxy-1,4-anthraquinone, a benzannelated juglone derivative, undergoes regiospecific cycloaddition with isoprene when conducted in the presence of boron triacetate. The structure of this regiomer has been determined by X-ray crystallography.
dc.description.statementofresponsibilityRichard A. Russell, Geoffrey J. Collin, Meta Sterns, Ronald N. Warrener
dc.identifier.citationTetrahedron Letters: the international journal for the rapid publication of all preliminary communications in organic chemistry, 1979; 20(43):4229-4232
dc.identifier.doi10.1016/S0040-4039(01)86552-7
dc.identifier.issn0040-4039
dc.identifier.issn1873-3581
dc.identifier.urihttp://hdl.handle.net/2440/85862
dc.language.isoen
dc.publisherPergamon Press
dc.rights© Pergamon Press Ltd. 1979.
dc.source.urihttps://doi.org/10.1016/s0040-4039(01)86552-7
dc.titleCycloaddition routes to polycyclic quinones: Part 1 boron triacetate as a regiochemical directing agent
dc.typeJournal article
pubs.publication-statusPublished

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