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Correction: Enantioselective C(sp3)–H bond functionalization enabled by CpxM(III) catalysis (M = Co, Rh, Ir)
Shu-Bin
Mou†
ab,
Mu-Peng
Luo†
b,
Feifei
Fang†
b,
Shi
Cao
*b,
Dong
Wu
*a and
Shou-Guo
Wang
*b
aComputer Aided Drug Discovery Center, Zhuhai Institute of Advanced Technology, Chinese Academy of Sciences, Zhuhai 519003, P. R. China. E-mail: wudong@ziat.ac.cn
bCollege of Chemistry and Environmental Engineering, Shenzhen University, Shenzhen 518060, P. R. China. E-mail: shicaorganic@szu.edu.cn; shouguo.wang@szu.edu.cn
First published on 24th February 2026
Abstract
Correction for ‘Enantioselective C(sp3)–H bond functionalization enabled by CpxM(III) catalysis (M = Co, Rh, Ir)’ by Shu-Bin Mou et al., Chem. Sci., 2026, 17, 2990–3004, https://doi.org/10.1039/d5sc08394j.
The authors regret that three of the schemes in the published manuscript (Schemes 16, 20 and 21) had errors present in them. The corrected schemes are given below.
 | ||
| Scheme 1 Rh(III)-catalyzed asymmetric intermolecular allylic C–H amination of unactivated alkenes. | ||
 | ||
| Scheme 2 Rh(III)-catalyzed asymmetric allylic C–H alkylation of α-olefins. | ||
 | ||
| Scheme 3 Co(III)/CCA-catalyzed enantioselective C(sp3)–H amidation of thioamides. | ||
The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.
Footnote |
| † These authors contributed equally. |
| This journal is © The Royal Society of Chemistry 2026 |