Enantioselective total syntheses of the alkaloids (−)-rhazinal, (−)-rhazinilam, (−)-leuconolam and (+)- epi -leuconolam

dc.contributor.authorBanwell, Martin
dc.contributor.authorBeck, Daniel
dc.contributor.authorWillis, Anthony
dc.date.accessioned2015-12-13T22:45:23Z
dc.date.issued2006
dc.date.updated2015-12-11T10:21:13Z
dc.description.abstractThe title alkaloids, (-)-1, (-)-2, (-)-4 and (+)-5 respectively, have each been prepared from the enantiomerically enriched (74% ee) tetrahydroindolizine 14 which is itself obtained via an organocatalyzed and enantioselective intramolecular Michael addition reaction of the pyrrole 13 incorporating an N-tethered and β,β-disubstituted acrylaldehyde moiety.
dc.identifier.issn1551-7004
dc.identifier.urihttp://hdl.handle.net/1885/79743
dc.publisherARKAT Foundation
dc.sourceARKIVOC
dc.source.urihttp://www.arkat-usa.org/home.aspx?VIEW=MANUSCRIPT&MSID=1602
dc.subject(+)-epi-leuconolam
dc.subject(-)-leuconolam
dc.subject(-)-rhazinal
dc.subject(-)-rhazinilam
dc.subjectEnantioselective
dc.subjectTotal synthesis
dc.titleEnantioselective total syntheses of the alkaloids (−)-rhazinal, (−)-rhazinilam, (−)-leuconolam and (+)- epi -leuconolam
dc.typeJournal article
local.bibliographicCitation.issueiii
local.bibliographicCitation.lastpage174
local.bibliographicCitation.startpage163
local.contributor.affiliationBanwell, Martin, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationBeck, Daniel, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationWillis, Anthony, College of Physical and Mathematical Sciences, ANU
local.contributor.authoruidBanwell, Martin, u9500594
local.contributor.authoruidBeck, Daniel, u4016782
local.contributor.authoruidWillis, Anthony, u8512028
local.description.embargo2037-12-31
local.description.notesImported from ARIES
local.description.refereedYes
local.identifier.absfor030503 - Organic Chemical Synthesis
local.identifier.ariespublicationMigratedxPub8125
local.identifier.citationvolume2006
local.identifier.scopusID2-s2.0-27644502443
local.type.statusPublished Version

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