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Chemoenzymatic approaches to the montanine alkaloids: a total synthesis of (+)-brunsvigine

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dc.contributor.authorBanwell, Martin
dc.contributor.authorKokas, Okanya
dc.contributor.authorWillis, Anthony
dc.date.accessioned2015-12-08T22:25:00Z
dc.date.issued2007
dc.date.updated2015-12-08T09:01:17Z
dc.description.abstractThe readily available and enzymatically derived cis-1,2-dihydrocatechols 3a and 3b have been elaborated over 17 steps, including a novel radical addition/elimination sequence, into the enantiomer, (+)-1, of the montanine alkaloid brunsvigine [(-)-1].
dc.identifier.issn1523-7060
dc.identifier.urihttp://hdl.handle.net/1885/33228
dc.publisherAmerican Chemical Society
dc.sourceOrganic Letters
dc.subjectKeywords: alkaloid; Amaryllidaceae alkaloid; brunsvigine; catechol derivative; isoquinoline derivative; montanine; unclassified drug; article; chemical structure; chemistry; stereoisomerism; synthesis; Alkaloids; Amaryllidaceae Alkaloids; Catechols; Isoquinolines;
dc.titleChemoenzymatic approaches to the montanine alkaloids: a total synthesis of (+)-brunsvigine
dc.typeJournal article
local.bibliographicCitation.issue18
local.bibliographicCitation.lastpage3506
local.bibliographicCitation.startpage3503
local.contributor.affiliationBanwell, Martin, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationKokas, Okanya, 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.authoruidKokas, Okanya, u4052054
local.contributor.authoruidWillis, Anthony, u8512028
local.description.embargo2037-12-31
local.description.notesImported from ARIES
local.identifier.absfor030503 - Organic Chemical Synthesis
local.identifier.ariespublicationu4005981xPUB100
local.identifier.citationvolume9
local.identifier.doi10.1021/ol071344y
local.identifier.scopusID2-s2.0-34548534948
local.type.statusPublished Version

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