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dc.contributor.authorStrieth-Kalthoff, Felix
dc.contributor.authorLongstreet, Ashley R.
dc.contributor.authorWeber, Jessica Marie
dc.contributor.authorJamison, Timothy F
dc.date.accessioned2020-06-23T19:07:24Z
dc.date.available2020-06-23T19:07:24Z
dc.date.issued2018-07
dc.identifier.issn1867-3899
dc.identifier.urihttps://hdl.handle.net/1721.1/125950
dc.description.abstractHerein, we introduce a new class of bench-stable N-heterocyclic carbene (NHC) nickel-precatalysts for homogeneous nickel-catalysis. The nickel(II) complexes are readily activated to Ni0 in situ under mild conditions, via a proposed Heck-type mechanism. The precatalysts are shown to facilitate carbonyl-ene, hydroalkenylation, and amination reactions.en_US
dc.description.sponsorshipNIH Ruth L. Kirschstein National Research Service Award (no. F32GM120852)en_US
dc.language.isoen
dc.publisherWileyen_US
dc.relation.isversionof10.1002/CCTC.201800454en_US
dc.rightsCreative Commons Attribution 4.0 International licenseen_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_US
dc.sourceWileyen_US
dc.titleBench-stable N -heterocyclic carbene nickel precatalysts for C−C and C−N bond-forming reactionsen_US
dc.typeArticleen_US
dc.identifier.citationStrieth-Kalthoff, Felix, et al., "Bench-stable N -heterocyclic carbene nickel precatalysts for C−C and C−N bond-forming reactions." ChemCatChem 10, 13 (July 2018): p. 2873-77 doi 10.1002/CCTC.201800454 ©2018 Author(s)en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.relation.journalChemCatChemen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2019-12-18T17:05:24Z
dspace.date.submission2019-12-18T17:05:26Z
mit.journal.volume10en_US
mit.journal.issue13en_US


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