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Phosphine complexes of an enantiomerically pure, atropisomeric arsenium ion

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dc.contributor.authorKilah, Nathan
dc.contributor.authorWild, Stanley (Bruce)
dc.date.accessioned2015-12-10T22:58:29Z
dc.date.issued2012
dc.date.updated2016-02-24T10:24:51Z
dc.description.abstractThe first enantiomerically pure secondary iodoarsine has been prepared by ring closure of (aR)-[{Li(TMEDA)}2{2,2′-bis(methylene)-1, 1′-binaphthylyl}] with dichlorophenylarsine, followed by disproportionation of the resulting seven-membered (aR)-phenyl
dc.identifier.issn0276-7333
dc.identifier.urihttp://hdl.handle.net/1885/60874
dc.publisherAmerican Chemical Society
dc.sourceOrganometallics
dc.subjectKeywords: Absolute configuration; Air-stable; Arsenic atom; Binaphthyl; Complex cation; Diastereomers; Disproportionations; H NMR spectra; Hexafluorophosphates; Methoxymethyl; Methylene groups; NMR spectrum; P-chiral phosphines; Phosphine complex; Phosphine exchang
dc.titlePhosphine complexes of an enantiomerically pure, atropisomeric arsenium ion
dc.typeJournal article
local.bibliographicCitation.lastpage2666
local.bibliographicCitation.startpage2658
local.contributor.affiliationKilah, Nathan, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationWild, Stanley (Bruce), College of Physical and Mathematical Sciences, ANU
local.contributor.authoruidKilah, Nathan, u4101782
local.contributor.authoruidWild, Stanley (Bruce), u7901996
local.description.embargo2037-12-31
local.description.notesImported from ARIES
local.identifier.absfor039904 - Organometallic Chemistry
local.identifier.absseo970103 - Expanding Knowledge in the Chemical Sciences
local.identifier.ariespublicationu4005981xPUB570
local.identifier.citationvolume31
local.identifier.doi10.1021/om200853d
local.identifier.scopusID2-s2.0-84859567134
local.identifier.thomsonID000303076600020
local.type.statusPublished Version

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