The Total Synthesis of the Galbulimima Alkaloid GB 13

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dc.contributor.authorMander, Lewis
dc.contributor.authorMcLachlan, Matthew
dc.date.accessioned2015-12-13T23:05:59Z
dc.date.available2015-12-13T23:05:59Z
dc.date.issued2003
dc.date.updated2015-12-12T08:03:12Z
dc.description.abstractThis contribution describes a synthetic approach to alkaloid GB 13, previously isolated from the North Australian and Papua New Guinean rain forest tree Galbulimima belgraveana. A Birch reductive alkylation of 2,5-dimethoxybenzoic acid by 3-methoxybenzyl
dc.identifier.issn0002-7863
dc.identifier.urihttp://hdl.handle.net/1885/85811
dc.publisherAmerican Chemical Society
dc.sourceJournal of the American Chemical Society
dc.subjectKeywords: alkaloid; ammonia; benzene derivative; galbulimima alkaloid gb 13; ketone; lithium; nitrile; unclassified drug; ytterbium; amination; article; catalysis; cyclization; Diels Alder reaction; epoxidation; hydrolysis; nuclear magnetic resonance spectroscopy;
dc.titleThe Total Synthesis of the Galbulimima Alkaloid GB 13
dc.typeJournal article
local.bibliographicCitation.issue9
local.bibliographicCitation.lastpage2401
local.bibliographicCitation.startpage2400
local.contributor.affiliationMander, Lewis, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationMcLachlan, Matthew, College of Physical and Mathematical Sciences, ANU
local.contributor.authoruidMander, Lewis, u7500768
local.contributor.authoruidMcLachlan, Matthew, u9617426
local.description.notesImported from ARIES
local.description.refereedYes
local.identifier.absfor030503 - Organic Chemical Synthesis
local.identifier.ariespublicationMigratedxPub14469
local.identifier.citationvolume125
local.identifier.doi10.1021/ja029725o
local.identifier.scopusID2-s2.0-0037420315
local.type.statusPublished Version

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