Experimental and theoretical investigation into the gold-catalyzed reactivity of cyclopropenylmethyl acetates

dc.contributor.authorSeraya, Elaineen
dc.contributor.authorSlack, Ericen
dc.contributor.authorAriafard, Alirezaen
dc.contributor.authorYates, Brian F.en
dc.contributor.authorHyland, Christopher J.T.en
dc.date.accessioned2025-07-08T11:29:47Z
dc.date.available2025-07-08T11:29:47Z
dc.date.issued2010-11-05en
dc.description.abstractCyclopropenylmethyl acetates have been shown to undergo rapid and stereoselective gold catalyzed rearrangement to Z-acetoxydienes in high yield. DFT calculations have shown that while several reaction pathways can be envisaged only a single, ring-opening one operates.en
dc.description.statusPeer-revieweden
dc.format.extent4en
dc.identifier.issn1523-7060en
dc.identifier.otherORCID:/0000-0003-2383-6380/work/163628686en
dc.identifier.scopus78049517580en
dc.identifier.urihttps://hdl.handle.net/1885/733766472
dc.language.isoenen
dc.sourceOrganic Lettersen
dc.titleExperimental and theoretical investigation into the gold-catalyzed reactivity of cyclopropenylmethyl acetatesen
dc.typeJournal articleen
dspace.entity.typePublicationen
local.bibliographicCitation.lastpage4771en
local.bibliographicCitation.startpage4768en
local.contributor.affiliationSeraya, Elaine; California State University Fullertonen
local.contributor.affiliationSlack, Eric; California State University Fullertonen
local.contributor.affiliationAriafard, Alireza; Research School of Chemistry, ANU College of Science and Medicine, The Australian National Universityen
local.contributor.affiliationYates, Brian F.; University of Tasmaniaen
local.contributor.affiliationHyland, Christopher J.T.; California State University Fullertonen
local.identifier.citationvolume12en
local.identifier.doi10.1021/ol101862uen
local.identifier.pure7b13dcfc-73f5-4411-b754-146996657bc0en
local.identifier.urlhttps://www.scopus.com/pages/publications/78049517580en
local.type.statusPublisheden

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