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Ring-Opening and -Expansion of 2,2'-Biaziridine: Access to Diverse Enantiopure Linear and Bicyclic Vicinal Diamines

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dc.contributor.authorBailey, Stephen J.
dc.contributor.authorWales, Steven M
dc.contributor.authorWillis, Anthony
dc.contributor.authorKeller, Paul
dc.date.accessioned2015-12-10T23:10:56Z
dc.date.issued2014
dc.date.updated2015-12-10T09:18:31Z
dc.description.abstractThe chiral pool-derived 1,1′-ditosyl-2,2′-biaziridine has been established as a valuable building block for the divergent synthesis of enantiopure vicinal diamines. Efficient procedures for the regioselective ring opening of the biaziridine with oxyge
dc.identifier.issn1523-7060
dc.identifier.urihttp://hdl.handle.net/1885/63610
dc.publisherAmerican Chemical Society
dc.sourceOrganic Letters
dc.titleRing-Opening and -Expansion of 2,2'-Biaziridine: Access to Diverse Enantiopure Linear and Bicyclic Vicinal Diamines
dc.typeJournal article
local.bibliographicCitation.issue16
local.bibliographicCitation.lastpage4347
local.bibliographicCitation.startpage4344
local.contributor.affiliationBailey, Stephen J., University of Wollongong
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.absfor030503 - Organic Chemical Synthesis
local.identifier.absfor030306 - Synthesis of Materials
local.identifier.absseo970103 - Expanding Knowledge in the Chemical Sciences
local.identifier.ariespublicationu4005981xPUB827
local.identifier.citationvolume16
local.identifier.doi10.1021/ol502164b
local.identifier.scopusID2-s2.0-84906266383
local.identifier.thomsonID000340517200073
local.type.statusPublished Version

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