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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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