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dc.contributor.authorLam, CC
dc.contributor.authorGoodman, JM
dc.date.accessioned2022-05-06T23:30:32Z
dc.date.available2022-05-06T23:30:32Z
dc.date.issued2022
dc.identifier.issn2052-4110
dc.identifier.urihttps://www.repository.cam.ac.uk/handle/1810/336800
dc.description.abstract<jats:p>The stereoselective reaction of 1,4-dicarbonyls with diarylprolinol silyl ether catalysts was studied with force field and density functional theory calculations.</jats:p>
dc.description.sponsorshipTrinity College
dc.publisherRoyal Society of Chemistry (RSC)
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleComputational insights on the origin of enantioselectivity in reactions with diarylprolinol silyl ether catalysts via a radical pathway
dc.typeArticle
dc.publisher.departmentDepartment of Chemistry
dc.date.updated2022-05-05T20:32:56Z
prism.publicationNameOrganic Chemistry Frontiers
dc.identifier.doi10.17863/CAM.84219
dcterms.dateAccepted2022-05-05
rioxxterms.versionofrecord10.1039/d2qo00354f
rioxxterms.versionVoR
dc.contributor.orcidLam, CC [0000-0001-7332-5656]
dc.contributor.orcidGoodman, JM [0000-0002-8693-9136]
dc.identifier.eissn2052-4129
rioxxterms.typeJournal Article/Review
pubs.funder-project-idEngineering and Physical Sciences Research Council (EP/P020259/1)
cam.issuedOnline2022
datacite.issupplementedby.urlhttps://doi.org/10.17863/CAM.84437
cam.orpheus.successTue Jun 21 09:21:02 BST 2022 - Embargo updated
cam.orpheus.counter3
cam.depositDate2022-05-05
pubs.licence-identifierapollo-deposit-licence-2-1
pubs.licence-display-nameApollo Repository Deposit Licence Agreement


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Attribution 4.0 International
Except where otherwise noted, this item's licence is described as Attribution 4.0 International