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dc.contributor.authorLee, Shao-Chi
dc.contributor.authorGuo, Lin
dc.contributor.authorRueping, Magnus
dc.date.accessioned2019-12-10T05:30:50Z
dc.date.available2019-12-10T05:30:50Z
dc.date.issued2019
dc.identifier.citationLee, S.-C., Guo, L., & Rueping, M. (2019). Nickel-catalyzed exo-selective hydroacylation/Suzuki cross-coupling reaction. Chemical Communications. doi:10.1039/c9cc07558e
dc.identifier.doi10.1039/c9cc07558e
dc.identifier.urihttp://hdl.handle.net/10754/660487
dc.description.abstractThe first nickel-catalyzed intramolecular hydroacylation/Suzuki cross coupling cascade of o-allylbenzaldehydes with a broad range of phenylboronic acid neopentyl glycol esters has been developed. This strategy shows high regioselectivity and step economy in the construction of two C-C bonds via aldehyde C-H bond activation, affording valuable indanones with high efficiency.
dc.publisherRoyal Society of Chemistry (RSC)
dc.relation.urlhttp://xlink.rsc.org/?DOI=C9CC07558E
dc.rightsArchived with thanks to Chemical communications (Cambridge, England)
dc.titleNickel-catalyzed exo-selective hydroacylation/Suzuki cross-coupling reaction.
dc.typeArticle
dc.contributor.departmentChemical Science Program
dc.contributor.departmentKAUST Catalysis Center (KCC)
dc.contributor.departmentPhysical Science and Engineering (PSE) Division
dc.identifier.journalChemical communications (Cambridge, England)
dc.rights.embargodate2020-11-29
dc.eprint.versionPost-print
dc.contributor.institutionInstitute of Organic Chemistry, RWTH Aachen University, Landoltweg 1, 52074, Aachen, Germany.
kaust.personRueping, Magnus
refterms.dateFOA2020-11-29T00:00:00Z


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