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The Total Synthesis of the Galbulimima Alkaloid GB 13

Mander, Lewis; McLachlan, Matthew

Description

This 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.contributor.authorMander, Lewis
dc.contributor.authorMcLachlan, Matthew
dc.date.accessioned2015-12-13T23:05:59Z
dc.date.available2015-12-13T23:05:59Z
dc.identifier.issn0002-7863
dc.identifier.urihttp://hdl.handle.net/1885/85811
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.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.description.notesImported from ARIES
local.description.refereedYes
local.identifier.citationvolume125
dc.date.issued2003
local.identifier.absfor030503 - Organic Chemical Synthesis
local.identifier.ariespublicationMigratedxPub14469
local.type.statusPublished Version
local.contributor.affiliationMander, Lewis, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationMcLachlan, Matthew, College of Physical and Mathematical Sciences, ANU
local.bibliographicCitation.issue9
local.bibliographicCitation.startpage2400
local.bibliographicCitation.lastpage2401
local.identifier.doi10.1021/ja029725o
dc.date.updated2015-12-12T08:03:12Z
local.identifier.scopusID2-s2.0-0037420315
CollectionsANU Research Publications

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