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dc.contributor.authorCallingham, Michael
dc.contributor.authorPartridge, Benjamin M.
dc.contributor.authorLewis, William
dc.contributor.authorLam, Hon Wai
dc.date.accessioned2017-10-10T16:42:54Z
dc.date.available2017-10-10T16:42:54Z
dc.date.issued2017-10-10
dc.identifier.urihttps://rdmc.nottingham.ac.uk/handle/internal/334
dc.description.abstractRaw data for new compounds described in the paper: "Enantioselective rhodium-catalyzed coupling of arylboronic acids, 1,3-enynes, and imines by alkenyl-to-allyl 1,4-rhodium(I) migration".en_UK
dc.language.isoenen_UK
dc.publisherThe University of Nottinghamen_UK
dc.subject.lcshAsymmetry (Chemistry)en_UK
dc.subject.lcshEnantioselective catalysisen_UK
dc.subject.lcshIminesen_UK
dc.subject.lcshIsomerizationen_UK
dc.subject.lcshRhodiumen_UK
dc.titleRaw data for new compounds described in the paper: "Enantioselective rhodium-catalyzed coupling of arylboronic acids, 1,3-enynes, and imines by alkenyl-to-allyl 1,4-rhodium(I) migration"en_UK
dc.identifier.doihttp://doi.org/10.17639/nott.330
dc.subject.freeallylation, asymmetric catalysis, imine, isomerization, rhodiumen_UK
dc.subject.jacsPhysical sciences::Chemistry::Organic chemistryen_UK
dc.subject.lcQ Science::QD Chemistry::QD241 Organic chemistryen_UK
uon.divisionUniversity of Nottingham, UK Campus::Faculty of Science::School of Chemistryen_UK
uon.funder.controlledEngineering & Physical Sciences Research Councilen_UK
uon.datatypeIR, NMR, mass spectrometry, and HPLC dataen_UK
uon.funder.freeEuropean Research Councilen_UK
uon.funder.freeGlaxoSmithKlineen_UK
uon.funder.freeThe University of Nottinghamen_UK
uon.grantStarting Grant No. 258580en_UK
uon.grantEP/I004769/1en_UK
uon.grantEP/I004769/2en_UK
uon.collectionmethodUsing IR, NMR, and mass spectrometers, and HPLC machinesen_UK
uon.preservation.rarelyaccessedtrue
dc.relation.doi10.1002/anie.201709334en_UK


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