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dc.contributor.authorPaterson, Ianen_US
dc.contributor.authorJ. Coster, Marken_US
dc.date.accessioned2017-04-24T12:47:59Z
dc.date.available2017-04-24T12:47:59Z
dc.date.issued2002en_US
dc.date.modified2009-04-20T04:47:01Z
dc.identifier.issn00404039en_US
dc.identifier.doi10.1016/S0040-4039(02)00527-0en_AU
dc.identifier.urihttp://hdl.handle.net/10072/22614
dc.description.abstractThe CD-spiroacetal contg. C16-C28 subunit I, as used in the total synthesis of the potent cytotoxic macrolide altohyrtin A (spongistatin 1), was prepd. by an alternative route using substrate-based stereocontrol in the two aldol bond constructions generating the acyclic precursor II.en_US
dc.description.peerreviewedYesen_US
dc.description.publicationstatusYesen_AU
dc.languageEnglishen_US
dc.language.isoen_AU
dc.publisherElsevier Ltden_US
dc.publisher.placeOxford, UKen_US
dc.publisher.urihttp://www.sciencedirect.com/science/journal/00404039en_AU
dc.relation.ispartofpagefrom3285en_US
dc.relation.ispartofpageto3289en_US
dc.relation.ispartofjournalTetrahedron Lettersen_US
dc.relation.ispartofvolume43en_US
dc.subject.fieldofresearchcode250301en_US
dc.titleTotal synthesis of altohyrtin A (spongistatin 1): an alternative synthesis of the CD-spiroacetal subunit.en_US
dc.typeJournal articleen_US
dc.type.descriptionC1 - Peer Reviewed (HERDC)en_US
dc.type.codeC - Journal Articlesen_US
gro.date.issued2002
gro.hasfulltextNo Full Text


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