Chemical shift and coupling constant analysis of dibenzyloxy disulfides

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dc.contributor.authorStoutenburg, Eric G.
dc.contributor.authorGryn'ova, Ganna
dc.contributor.authorCoote, Michelle
dc.contributor.authorPriefer, Ronny
dc.date.accessioned2015-12-10T23:11:52Z
dc.date.issued2015
dc.date.updated2015-12-10T09:24:50Z
dc.description.abstractDialkoxy disulfides have found applications in the realm of organic synthesis as an S2 or alkoxy donor, under thermal and photolytic decompositions conditions, respectively. Spectrally, dibenzyloxy disulfides possess an ABq in the 1H NMR, which can shift
dc.identifier.issn1386-1425
dc.identifier.urihttp://hdl.handle.net/1885/63875
dc.publisherElsevier
dc.sourceSpectrochimica Acta: part A
dc.titleChemical shift and coupling constant analysis of dibenzyloxy disulfides
dc.typeJournal article
local.bibliographicCitation.issuePart C
local.bibliographicCitation.lastpage1931
local.bibliographicCitation.startpage1924
local.contributor.affiliationStoutenburg, Eric G., Niagara University
local.contributor.affiliationGryn'ova, Ganna, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationCoote, Michelle, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationPriefer, Ronny, Niagara University
local.contributor.authoruidGryn'ova, Ganna, u4768988
local.contributor.authoruidCoote, Michelle, u4031074
local.description.embargo2037-12-31
local.description.notesImported from ARIES
local.identifier.absfor030701 - Quantum Chemistry
local.identifier.absseo970103 - Expanding Knowledge in the Chemical Sciences
local.identifier.ariespublicationu4005981xPUB858
local.identifier.citationvolume136
local.identifier.doi10.1016/j.saa.2014.10.109
local.identifier.scopusID2-s2.0-84923878369
local.type.statusPublished Version

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