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A chemoenzymatic total synthesis of the structure assigned to the alkaloid (+)-montabuphine

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dc.contributor.authorMatveenko, Maria
dc.contributor.authorBanwell, Martin
dc.contributor.authorWillis, Anthony
dc.date.accessioned2015-12-10T22:22:05Z
dc.date.issued2008
dc.date.updated2016-02-24T10:22:49Z
dc.description.abstract(Chemical Equation Presented) An enantioselective synthesis of the structure, 3, assigned to the alkaloid (+)-montabuphine has been achieved using the readily available metabolite 4 as starting material. A comparison of the physical and spectral data recorded on compound 3 with those reported for (+)-montabuphine suggests that they are different compounds.
dc.identifier.issn1523-7060
dc.identifier.urihttp://hdl.handle.net/1885/52498
dc.publisherAmerican Chemical Society
dc.sourceOrganic Letters
dc.subjectKeywords: alkaloid; Amaryllidaceae alkaloid; enzyme; montabuphine; unclassified drug; article; chemical structure; chemistry; metabolism; nuclear magnetic resonance spectroscopy; synthesis; Alkaloids; Amaryllidaceae Alkaloids; Enzymes; Magnetic Resonance Spectrosco
dc.titleA chemoenzymatic total synthesis of the structure assigned to the alkaloid (+)-montabuphine
dc.typeJournal article
local.bibliographicCitation.issue20
local.bibliographicCitation.lastpage4396
local.bibliographicCitation.startpage4693
local.contributor.affiliationMatveenko, Maria, 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.authoruidMatveenko, Maria, u4195285
local.contributor.authoruidBanwell, Martin, u9500594
local.contributor.authoruidWillis, Anthony, u8512028
local.description.embargo2037-12-31
local.description.notesImported from ARIES
local.identifier.absfor030503 - Organic Chemical Synthesis
local.identifier.absfor030502 - Natural Products Chemistry
local.identifier.ariespublicationu4005981xPUB248
local.identifier.citationvolume10
local.identifier.doi10.1021/ol801815k
local.identifier.scopusID2-s2.0-58149173852
local.identifier.thomsonID000259940600076
local.type.statusPublished Version

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