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Reversible aqueous metathesis reactions for potential application in dynamic combinatorial chemistry

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dc.contributor.authorHunter, Luke
dc.contributor.authorCondie, Glenn C
dc.contributor.authorHarding, Margaret
dc.date.accessioned2015-12-13T22:26:39Z
dc.date.issued2010
dc.date.updated2016-02-24T09:15:43Z
dc.description.abstractSolutions of heterocycles having an allyl sulfide unit and simple alkenes in 50% t-BuOH/H2O undergo reversible olefin metathesis reactions with the second generation Hoveyda-Grubbs catalyst. The choice of functional groups is limited by competitive chelation of some heterocycles with the catalyst, and other stereoelectronic effects.
dc.identifier.issn0040-4039
dc.identifier.urihttp://hdl.handle.net/1885/73600
dc.publisherElsevier
dc.sourceTetrahedron Letters
dc.subjectKeywords: alkene; allyl compound; naphthalimide derivative; article; catalyst; chelation; chemical reaction; combinatorial chemistry; metathesis reaction; stereochemistry Allyl sulfides; Aqueous metathesis; Dynamic combinatorial chemistry; Reversible metathesis
dc.titleReversible aqueous metathesis reactions for potential application in dynamic combinatorial chemistry
dc.typeJournal article
local.bibliographicCitation.issue38
local.bibliographicCitation.lastpage5067
local.bibliographicCitation.startpage5064
local.contributor.affiliationHunter, Luke, University of Sydney
local.contributor.affiliationCondie, Glenn C, University of Sydney
local.contributor.affiliationHarding, Margaret, Administrative Division, ANU
local.contributor.authoruidHarding, Margaret, u4044881
local.description.embargo2037-12-31
local.description.notesImported from ARIES
local.identifier.absfor030500 - ORGANIC CHEMISTRY
local.identifier.ariespublicationf5625xPUB3754
local.identifier.citationvolume51
local.identifier.doi10.1016/j.tetlet.2010.07.105
local.identifier.scopusID2-s2.0-78549273321
local.identifier.thomsonID000281626100038
local.type.statusPublished Version

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