Probing for the pharmacophore of the cytotoxic neoclerodane salvileucalin B

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dc.contributor.authorHeinrich, Nora
dc.contributor.authorBanwell, Martin
dc.contributor.authorWillis, Anthony
dc.contributor.authorCade, Ian
dc.contributor.authorCapon, Robert J
dc.contributor.authorHuang, Xiao-Cong
dc.date.accessioned2015-12-10T23:01:39Z
dc.date.issued2012
dc.date.updated2016-02-24T10:25:25Z
dc.description.abstractThe novel [4.3.1]propelladiene 2, which embodies the key structural elements of the pentacyclic core of the cytotoxic neoclerodane salvileucalin B (1), has been prepared using a rhodium-catalysed intramolecular Bchner reaction as the key step. Compound 2
dc.identifier.issn0004-9425
dc.identifier.urihttp://hdl.handle.net/1885/61688
dc.publisherCSIRO Publishing
dc.sourceAustralian Journal of Chemistry
dc.subjectKeywords: Cytotoxic; Human cancer cells; Pharmacophores; Structural elements; Cell culture; Rhodium
dc.titleProbing for the pharmacophore of the cytotoxic neoclerodane salvileucalin B
dc.typeJournal article
local.bibliographicCitation.issue12
local.bibliographicCitation.lastpage1686
local.bibliographicCitation.startpage1679
local.contributor.affiliationHeinrich, Nora, 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.affiliationCade, Ian, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationCapon, Robert J, University of Queensland
local.contributor.affiliationHuang, Xiao-Cong, University of Queensland
local.contributor.authoremailu9500594@anu.edu.au
local.contributor.authoruidHeinrich, Nora, u4472825
local.contributor.authoruidBanwell, Martin, u9500594
local.contributor.authoruidWillis, Anthony, u8512028
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.ariespublicationu4005981xPUB631
local.identifier.citationvolume65
local.identifier.doi10.1071/CH12358
local.identifier.scopusID2-s2.0-84871583901
local.identifier.thomsonID000312163400017
local.identifier.uidSubmittedByu4005981
local.type.statusPublished Version

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