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Published on: August 18, 2020
Light/Palladium-Promoted Benzylic C-H Acylation Using a Benzoyl Group as the Photo-Directing Group
Yusuke Masuda1, Naoki Ishida1, Masahiro Murakami1
1Department of Synthetic Chemistry and Biological Chemistry, Kyoto University, Katsura, Kyoto, 615-8510, Japan.
Abstract:
2-Methylphenyl ketones undergo site-selective acylation at the benzylic position when treated with acid anhydride under UV irradiation in the presence of a palladium catalyst. The benzoyl carbonyl group serves as the photo-directing group so that the ortho benzylic C-H bond is activated site-selectively.
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