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Correction: Palladium catalyzed amide-oxazoline directed C–H acetoxylation of arenes

Bin Liu , Xuhu Huang , Xin Wang , Zemei Ge * and Runtao Li *
State Key Laboratory of Natural and Biomimetic Drugs, Peking University, Beijing 100191, China. E-mail: lirt@bjmu.edu.cn

First published on 27th May 2015


Abstract

Correction for ‘Palladium catalyzed amide-oxazoline directed C–H acetoxylation of arenes’ by Bin Liu et al., Org. Chem. Front., 2015, DOI: 10.1039/c5qo00104h.


In 2013, Zhang and co-workers developed the Pd-catalyzed oxidative acetoxylation of benzylic C(sp3)–H bonds of picolinoyl-protected toluidines using PhI(OAc)2 as an oxidant.1 In our article, we regret the inclusion of an incorrect structure in Scheme 1, page 1 of the original manuscript. The correct structures are given below.
image file: c5qo90028j-s1.tif
Scheme 1 Transition metal-catalyzed acetoxylation of C–H bonds.

The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.

References

  1. L. Ju, J.-Z. Yao, Z.-H. Wu, Z.-X. Liu and Y.-H. Zhang, J. Org. Chem., 2013, 78, 10821 CrossRef CAS PubMed.

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