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Published on: July 28, 2022
Intermolecular chemo- and regioselective aromatic C-H amination of alkoxyarenes promoted by rhodium nitrenoids
Kenta Arai1, Yoshihiro Ueda, Kazuhiro Morisaki
1Institute for Chemical Research, Kyoto University, Uji, Kyoto 611-0011, Japan. ueda@fos.kuicr.kyoto-u.ac.jp kawabata@scl.kyoto-u.ac.jp.
Abstract:
Intermolecular aromatic C(sp2)-H amination promoted by neutral rhodium nitrenoids has been developed. The reactions proceeded with various oxygen-substituted arenes (1.5 equiv.) in a chemo- and regioselective manner. The aromatic C(sp2)-H amination took place at the para position of the oxygen substituent in the presence of benzylic C(sp3)-H bonds and/or C(sp3)-H bonds α to ethereal oxygen.
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