Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/143930
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dc.contributor.authorXu, Wengangen_US
dc.contributor.authorYoshikai, Naohikoen_US
dc.date.accessioned2020-10-02T01:01:01Z-
dc.date.available2020-10-02T01:01:01Z-
dc.date.issued2019-
dc.identifier.citationXu, W., & Yoshikai, N. (2019). Iron-catalyzed ortho C−H arylation and methylation of pivalophenone N−H imines. ChemSusChem, 12(13), 3049-3053. doi:10.1002/cssc.201900164en_US
dc.identifier.issn1864-5631en_US
dc.identifier.urihttps://hdl.handle.net/10356/143930-
dc.description.abstractIron‐catalyzed ortho C−H arylation and methylation reactions of pivalophenone N−H imines are reported. The pivaloyl N−H imine proved an excellent directing group for the arylation with diarylzinc reagents in the presence of an iron‐diphosphine catalyst and 2,3‐dichlorobutane at room temperature. A similar catalytic system also allowed methylation with Me3Al at 70 °C. The pivaloyl imine of the product could be readily converted to a cyano group, thus allowing convenient preparation of ortho‐functionalized benzonitriles.en_US
dc.description.sponsorshipMinistry of Education (MOE)en_US
dc.description.sponsorshipNanyang Technological Universityen_US
dc.language.isoenen_US
dc.relation.ispartofChemSusChemen_US
dc.rightsThis is the accepted version of the following article: Xu, W., & Yoshikai, N. (2019). Iron-catalyzed ortho C−H arylation and methylation of pivalophenone N−H imines. ChemSusChem, 12(13), 3049-3053. doi:10.1002/cssc.201900164, which has been published in final form at http://doi.org/10.1002/cssc.201900164. This article may be used for non-commercial purposes in accordance with the Wiley Self-Archiving Policy [https://authorservices.wiley.com/authorresources/Journal-Authors/licensing/self-archiving.html].en_US
dc.subjectScience::Chemistryen_US
dc.titleIron-catalyzed ortho C−H arylation and methylation of pivalophenone N−H iminesen_US
dc.typeJournal Articleen
dc.contributor.schoolSchool of Physical and Mathematical Sciencesen_US
dc.identifier.doi10.1002/cssc.201900164-
dc.description.versionAccepted versionen_US
dc.identifier.pmid30786170-
dc.identifier.issue13en_US
dc.identifier.volume12en_US
dc.identifier.spage3049en_US
dc.identifier.epage3053en_US
dc.subject.keywordsArylationen_US
dc.subject.keywordsC−H Activationen_US
dc.description.acknowledgementThis work was supported by the Ministry of Education (Singapore) and Nanyang Technological University (MOE2016-T2-2-043)en_US
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