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dc.contributor.authorAbdel-Magied, Ahmed F.
dc.contributor.authorSingh, Amrendra K.
dc.contributor.authorHaukka, Matti
dc.contributor.authorRichmond, Michael G.
dc.contributor.authorNordlander, Ebbe
dc.date.accessioned2016-02-04T12:42:47Z
dc.date.available2016-02-04T12:42:47Z
dc.date.issued2014
dc.identifier.citationAbdel-Magied, A. F., Singh, A. K., Haukka, M., Richmond, M. G., & Nordlander, E. (2014). Diastereomeric control of enantioselectivity: evidence for metal cluster catalysis. <i>Chemical Communications</i>, <i>50</i>(57), 7705-7708. <a href="https://doi.org/10.1039/c4cc02319f" target="_blank">https://doi.org/10.1039/c4cc02319f</a>
dc.identifier.otherCONVID_23758306
dc.identifier.otherTUTKAID_62342
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/48628
dc.description.abstractEnantioselective hydrogenation of tiglic acid effected by diastereomers of the general formula [(μ-H)2Ru3(μ3-S)(CO)7(μ-P–P*)] (P–P* = chiral Walphos diphosphine ligand) strongly supports catalysis by intact Ru3 clusters. A catalytic mechanism involving Ru3 clusters has been established by DFT calculations.
dc.language.isoeng
dc.publisherR S C Publications
dc.relation.ispartofseriesChemical Communications
dc.subject.otherhydrogenation catalysis
dc.subject.othertriruthenium clusters
dc.subject.otherintact
dc.titleDiastereomeric control of enantioselectivity: evidence for metal cluster catalysis
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-201602041437
dc.contributor.laitosKemian laitosfi
dc.contributor.laitosDepartment of Chemistryen
dc.contributor.oppiaineEpäorgaaninen ja analyyttinen kemiafi
dc.contributor.oppiaineInorganic and Analytical Chemistryen
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.date.updated2016-02-04T10:15:06Z
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatuspeerReviewed
dc.format.pagerange7705-7708
dc.relation.issn1359-7345
dc.relation.numberinseries57
dc.relation.volume50
dc.type.versionacceptedVersion
dc.rights.copyright© The Royal Society of Chemistry 2014. This is a final draft version of an article whose final and definitive form has been published by RSC. Published in this repository with the kind permission of the publisher.
dc.rights.accesslevelopenAccessfi
dc.relation.doi10.1039/c4cc02319f
dc.type.okmA1


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