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Synthesis of the enantiomer of the structure assigned to the natural product nobilisitine A

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dc.contributor.authorSchwartz, Brett
dc.contributor.authorJones, Matthew
dc.contributor.authorBanwell, Martin
dc.contributor.authorCade, Ian
dc.date.accessioned2015-12-10T22:41:21Z
dc.date.issued2010
dc.date.updated2016-02-24T10:23:42Z
dc.description.abstractThe synthesis of the enantiomer of the structure, 1, assigned to the natural product nobilisitine A has been accomplished using the enantiomerically pure cis-1,2-dihydrocatechol 4 as starting material. The1H and13C NMR spectral data derived from compound
dc.identifier.issn1523-7060
dc.identifier.urihttp://hdl.handle.net/1885/57860
dc.publisherAmerican Chemical Society
dc.sourceOrganic Letters
dc.subjectKeywords: alkaloid; biological product; fused heterocyclic rings; nobilisitine A; angiosperm; article; chemical structure; chemistry; nuclear magnetic resonance; stereoisomerism; synthesis; Alkaloids; Biological Products; Heterocyclic Compounds with 4 or More Rings
dc.titleSynthesis of the enantiomer of the structure assigned to the natural product nobilisitine A
dc.typeJournal article
local.bibliographicCitation.issue22
local.bibliographicCitation.lastpage5213
local.bibliographicCitation.startpage5210
local.contributor.affiliationSchwartz, Brett, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationJones, Matthew, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationBanwell, Martin, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationCade, Ian, College of Physical and Mathematical Sciences, ANU
local.contributor.authoruidSchwartz, Brett, u4691352
local.contributor.authoruidJones, Matthew, u4193049
local.contributor.authoruidBanwell, Martin, u9500594
local.contributor.authoruidCade, Ian, u4429837
local.description.embargo2037-12-31
local.description.notesImported from ARIES
local.identifier.absfor030503 - Organic Chemical Synthesis
local.identifier.absseo970103 - Expanding Knowledge in the Chemical Sciences
local.identifier.ariespublicationu4005981xPUB418
local.identifier.citationvolume12
local.identifier.doi10.1021/ol102249q
local.identifier.scopusID2-s2.0-78449295979
local.identifier.thomsonID000284080400034
local.type.statusPublished Version

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