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The first syntheses of enantiopure 2,2'-biindoline

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dc.contributor.authorWales, Steven M
dc.contributor.authorWillis, Anthony
dc.contributor.authorKeller, Paul
dc.date.accessioned2015-12-10T22:41:26Z
dc.date.issued2010
dc.date.updated2016-02-24T10:23:44Z
dc.description.abstractThe first two syntheses of chiral 2,2′-biindoline are reported either in five steps from 2,2′-bioxirane, or three steps from 2,2′-biaziridine, both with exceptional enantiopurity.
dc.identifier.issn1359-7345
dc.identifier.urihttp://hdl.handle.net/1885/57909
dc.publisherRoyal Society of Chemistry
dc.sourceChemical Communications
dc.subjectKeywords: 2,2' biaziridine; 2,2' biindoline; 2,2' bioxirane; amine; copper; iodide ion; palladium; silica gel; unclassified drug; addition reaction; amination; article; catalysis; chemical analysis; chemical structure; column chromatography; crystallization; enanti
dc.titleThe first syntheses of enantiopure 2,2'-biindoline
dc.typeJournal article
local.bibliographicCitation.issue48
local.bibliographicCitation.lastpage9228
local.bibliographicCitation.startpage9226
local.contributor.affiliationWales, Steven M, University of Wollongong
local.contributor.affiliationWillis, Anthony, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationKeller, Paul, University of Wollongong
local.contributor.authoruidWillis, Anthony, u8512028
local.description.embargo2037-12-31
local.description.notesImported from ARIES
local.identifier.absfor030606 - Structural Chemistry and Spectroscopy
local.identifier.absfor030503 - Organic Chemical Synthesis
local.identifier.absseo970103 - Expanding Knowledge in the Chemical Sciences
local.identifier.ariespublicationu4005981xPUB420
local.identifier.citationvolume46
local.identifier.doi10.1039/c0cc04045b
local.identifier.scopusID2-s2.0-78649653846
local.identifier.thomsonID000284774500043
local.type.statusPublished Version

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