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|Abstract:||© 2018 The Royal Society of Chemistry. In the original manuscript, we reported that CptRh(III) complexes enable the highly regioselective coupling of simple alkenes with benzhydroxamate esters forming predominantly the products of 3-substituted dihydroisoquinolones. It has come to our attention that we misassigned the structures and the reaction provides 4-substituted dihydroisoquinolones (the product that we had initially assigned as the minor isomer has proven to be the major isomer). Thus, while the yields and regioselectivities as reported are unchanged, the assignment of the major isomer must be corrected. We are grateful to Professor Dmitry Perekalin (Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences) for bringing this matter to our attention. The authors regret the error. The original ESI was replaced by a correspondingly revised version on 9th October 2018. In addition, the authors wish to provide updated affiliation and contact details, and as such affiliation b has been added to the corresponding author of this article. Full details may be found herein. The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers. (Figure Presented).|
|Citation:||Hyster, T.K., Dalton, D.M., Rovis, T. (2018). Correction: Ligand design for Rh(iii)-catalyzed C-H activation: An unsymmetrical cyclopentadienyl group enables a regioselective synthesis of dihydroisoquinolones (Chemical Science (2015) 6 (254-258) DOI: 10.1039/C4SC02590C). Chemical Science, 9 (41), 8024. doi:10.1039/c8sc90195c|
|Type of Material:||Journal Article|
|Journal/Proceeding Title:||Chemical Science|
|Version:||Final published version. This is an open access article.|
|Notes:||Chemical Science. Volume 9, Issue 41, 2018, Page 8024. First published on 15th October 2018.|
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