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The Structure of the Lycorenine Alkaloid Nobilisitine A

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dc.contributor.authorSchwartz, Brett
dc.contributor.authorWhite, Lorenzo
dc.contributor.authorBanwell, Martin
dc.contributor.authorWillis, Anthony
dc.date.accessioned2015-12-10T22:56:35Z
dc.date.issued2011
dc.date.updated2016-02-24T10:24:33Z
dc.description.abstractThe structure 3 recently proposed, on the basis of computed NMR chemical shifts, for the natural product nobilisitine A has been synthesized from its C5-epimer (+)-clividine (4). The spectral data derived from compound 3 match those reported for the natural product.
dc.identifier.issn0022-3263
dc.identifier.urihttp://hdl.handle.net/1885/60295
dc.publisherAmerican Chemical Society
dc.sourceJournal of Organic Chemistry
dc.subjectKeywords: Natural products; NMR chemical shifts; Spectral data; Amaryllidaceae alkaloid; lycorinine alkaloid; nobilisitine A; unclassified drug; article; carbon nuclear magnetic resonance; chemical reaction; chemical structure; diastereoisomer; epimer; fragmentatio
dc.titleThe Structure of the Lycorenine Alkaloid Nobilisitine A
dc.typeJournal article
local.bibliographicCitation.issue20
local.bibliographicCitation.lastpage8563
local.bibliographicCitation.startpage8560
local.contributor.affiliationSchwartz, Brett, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationWhite, Lorenzo, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationBanwell, Martin, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationWillis, Anthony, College of Physical and Mathematical Sciences, ANU
local.contributor.authoruidSchwartz, Brett, u4691352
local.contributor.authoruidWhite, Lorenzo, u4213207
local.contributor.authoruidBanwell, Martin, u9500594
local.contributor.authoruidWillis, Anthony, u8512028
local.description.embargo2037-12-31
local.description.notesImported from ARIES
local.identifier.absfor030502 - Natural Products Chemistry
local.identifier.absseo970103 - Expanding Knowledge in the Chemical Sciences
local.identifier.ariespublicationu4005981xPUB532
local.identifier.citationvolume76
local.identifier.doi10.1021/jo2016899
local.identifier.scopusID2-s2.0-80054120830
local.identifier.thomsonID000295816700052
local.type.statusPublished Version

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