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Correction: Nickel-catalyzed 1,4-aryl rearrangement of aryl N-benzylimidates via C–O and C–H bond cleavage
Satoshi
Ogawa
a and
Mamoru
Tobisu
*ab
aDepartment of Applied Chemistry, Graduate School of Engineering, Osaka University, Suita, Osaka 565-0871, Japan. E-mail: tobisu@chem.eng.osaka-u.ac.jp
bInnovative Catalysis Science Division, Institute for Open and Transdisciplinary Research Initiatives (ICS-OTRI), Osaka University, Suita, Osaka 565-0871, Japan
First published on 5th October 2022
Abstract
Correction for ‘Nickel-catalyzed 1,4-aryl rearrangement of aryl N-benzylimidates via C–O and C–H bond cleavage’ by Satoshi Ogawa et al., Chem. Commun., 2022, 58, 7909–7911, https://doi.org/10.1039/D2CC02355E.
The authors regret that there was an error in the original article. The kinetic isotope effect (kH/kD) value was given in the main text and in Scheme 2b as 2.4. The correct value is 4.2, as shown in the corrected Scheme 2 presented here. This does not affect the conclusions of the paper.
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| Scheme 2 Mechanistic studies. | ||
The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.
| This journal is © The Royal Society of Chemistry 2022 |