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Synthetic studies concerning the crinine alkaloid haemultine

Gao, Yuqian (Nadia); Ma, Xinghua; Petit, Laurent; Schwartz, Brett; Banwell, Martin; Willis, Anthony; Cade, Ian; Rae, A David

Description

The racemic form, (±)-1, of the structure originally assigned to the crinine alkaloid haemultine has been prepared for the first time. A key step involved the conversion of compound (±)-4 into the isomeric cis-C3a-arylhexahydroindole (±)-3 using a Pd0-

dc.contributor.authorGao, Yuqian (Nadia)
dc.contributor.authorMa, Xinghua
dc.contributor.authorPetit, Laurent
dc.contributor.authorSchwartz, Brett
dc.contributor.authorBanwell, Martin
dc.contributor.authorWillis, Anthony
dc.contributor.authorCade, Ian
dc.contributor.authorRae, A David
dc.date.accessioned2015-12-13T22:16:02Z
dc.identifier.issn0004-9425
dc.identifier.urihttp://hdl.handle.net/1885/70675
dc.description.abstractThe racemic form, (±)-1, of the structure originally assigned to the crinine alkaloid haemultine has been prepared for the first time. A key step involved the conversion of compound (±)-4 into the isomeric cis-C3a-arylhexahydroindole (±)-3 using a Pd0-
dc.publisherCSIRO Publishing
dc.sourceAustralian Journal of Chemistry
dc.subjectKeywords: Enantiomerically pure compounds; Intramolecular alder-ene reaction; Natural products; Paraformaldehydes; Pictet-Spengler reactions; Spectroscopic data; Synthetic study; Trifluoroacetic acids; Acetal resins; Enantiomers; Metabolites; Nitrogen compounds
dc.titleSynthetic studies concerning the crinine alkaloid haemultine
dc.typeJournal article
local.description.notesImported from ARIES
local.identifier.citationvolume66
dc.date.issued2013
local.identifier.absfor030503 - Organic Chemical Synthesis
local.identifier.ariespublicationf5625xPUB2378
local.type.statusPublished Version
local.contributor.affiliationGao, Yuqian (Nadia), College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationMa, Xinghua, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationPetit, Laurent, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationSchwartz, Brett, 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.affiliationRae, A David, College of Physical and Mathematical Sciences, ANU
local.description.embargo2037-12-31
local.bibliographicCitation.issue1
local.bibliographicCitation.startpage30
local.bibliographicCitation.lastpage39
local.identifier.doi10.1071/CH12473
local.identifier.absseo970103 - Expanding Knowledge in the Chemical Sciences
dc.date.updated2016-02-24T08:57:21Z
local.identifier.scopusID2-s2.0-84872856852
local.identifier.thomsonID000313753000005
CollectionsANU Research Publications

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