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Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/85947
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dc.contributor.authorRussell, R.A.-
dc.contributor.authorKrauss, A.S.-
dc.contributor.authorWarrener, R.N.-
dc.contributor.authorIrvine, R.W.-
dc.date.issued1984-
dc.identifier.citationTetrahedron Letters: the international journal for the rapid publication of all preliminary communications in organic chemistry, 1984; 25(14):1517-1520-
dc.identifier.issn0040-4039-
dc.identifier.issn1873-3581-
dc.identifier.urihttp://hdl.handle.net/2440/85947-
dc.description.abstractA comparison is made between two regiospecific modes of base-catalysed condensation of 4 (or 7)-methoxy-3-phenylsulfonyl phthalides with chiral bicyclic quinone monoketals, one of which occurs in 95% yield and forms the basis of the first enantiospecific total synthesis of (−)-7-deoxydaunomycinone (3).-
dc.description.statementofresponsibilityRichard A. Russell, Adrian S. Krauss, Ronald N. Warrener, Robert W. Irvine-
dc.language.isoen-
dc.publisherPergamon Press-
dc.rights© 1984 Pergamon Press Ltd.-
dc.source.urihttp://dx.doi.org/10.1016/s0040-4039(01)80201-x-
dc.titleA high-yielding enantiospecific synthesis of (-)-7-deoxydaunomycinone-
dc.typeJournal article-
dc.identifier.doi10.1016/S0040-4039(01)80201-X-
pubs.publication-statusPublished-
Appears in Collections:Aurora harvest 2
Chemistry publications

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