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Raw data for new compounds described in the paper: "Enantioselective nickel-catalyzed arylative intramolecular 1,4-allylations"

dc.contributor.authorLam, Hon Wai
dc.contributor.otherNguyen, Thi Le Nhon
dc.contributor.otherIncerti-Pradillos, Celia
dc.contributor.otherLewis, William
dc.date.accessioned2018-05-14T13:41:05Z
dc.date.available2018-05-14T13:41:05Z
dc.date.issued2018-05-14
dc.identifier.urihttps://rdmc.nottingham.ac.uk/handle/internal/358
dc.description.abstractRaw data for new compounds described in the paper: "Enantioselective nickel-catalyzed arylative intramolecular 1,4-allylations" The enantioselective nickel-catalyzed desymmetrization of allenyl cyclohexa-2,5-dienones by reaction with arylboronic acids is described. Nickel-catalyzed arylation of the allene gives allylnickel species, which undergo cyclization by 1,4-allylation to produce hexahydroindol-5-ones and hexahydrofuran-5-ones with three contiguous stereocenters in high diastereo- and enantioselectivities.en_UK
dc.language.isoenen_UK
dc.publisherRoyal Society of Chemistryen_UK
dc.subject.lcshChemicalsen_UK
dc.subject.lcshEnantioselective catalysisen_UK
dc.subject.lcshArylationen_UK
dc.subject.lcshAllenesen_UK
dc.titleRaw data for new compounds described in the paper: "Enantioselective nickel-catalyzed arylative intramolecular 1,4-allylations"en_UK
dc.identifier.doihttp://doi.org/10.17639/nott.354
dc.subject.freeRaw data for new compounds described in the paper: "Enantioselective nickel-catalyzed arylative intramolecular 1,4-allylations"en_UK
dc.subject.jacsPhysical sciences::Chemistry::Organic chemistry::Organometallic 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.controlledOtheren_UK
uon.datatypeIR, NMR, mass spectrometry, and HPLC dataen_UK
uon.funder.freeUniversity of Nottinghamen_UK
uon.funder.freeGlaxoSmithKlineen_UK
uon.collectionmethodUsing IR, NMR, and mass spectrometers, and HPLC machinesen_UK
uon.preservation.rarelyaccessedtrue
dc.relation.doi10.1039/C8CC03204Aen_UK


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