Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/143930
Title: Iron-catalyzed ortho C−H arylation and methylation of pivalophenone N−H imines
Authors: Xu, Wengang
Yoshikai, Naohiko
Keywords: Science::Chemistry
Issue Date: 2019
Source: 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
Journal: ChemSusChem
Abstract: Iron‐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.
URI: https://hdl.handle.net/10356/143930
ISSN: 1864-5631
DOI: 10.1002/cssc.201900164
Schools: School of Physical and Mathematical Sciences 
Rights: This 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].
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:SPMS Journal Articles

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