Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/82663
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dc.contributor.authorGuo, Siyuen
dc.contributor.authorYang, Pengen
dc.contributor.authorZhou, Jianrong Steveen
dc.date.accessioned2016-03-10T04:04:41Zen
dc.date.accessioned2019-12-06T14:59:55Z-
dc.date.available2016-03-10T04:04:41Zen
dc.date.available2019-12-06T14:59:55Z-
dc.date.issued2015en
dc.identifier.citationGuo, S., Yang, P., & Zhou, J. S. (2015). Nickel-catalyzed asymmetric transfer hydrogenation of conjugated olefins. Chemical Communications, 51(60), 12115-12117.en
dc.identifier.issn1359-7345en
dc.identifier.urihttps://hdl.handle.net/10356/82663-
dc.description.abstractAsymmetric transfer hydrogenation of electron-deficient olefins is realized with nickel catalysts supported by strongly σ-donating bisphosphines. Deuterium labeling experiments point to a reaction sequence of formate decarboxylation, asymmetric hydride insertion and non-stereoselective protonation of resulting nickel enolates.en
dc.format.extent3 p.en
dc.language.isoenen
dc.relation.ispartofseriesChemical Communicationsen
dc.rightsThis article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence.en
dc.subjectChemistry and Biological Chemistryen
dc.titleNickel-catalyzed asymmetric transfer hydrogenation of conjugated olefinsen
dc.typeJournal Articleen
dc.contributor.schoolSchool of Physical and Mathematical Sciencesen
dc.identifier.doi10.1039/C5CC01632Ken
dc.description.versionPublished versionen
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