Nedra Touja,
Abdullah S. Al-Ayedb,
Mathieu Sauthierc,
Lamjed Mansourd,
Abdel Halim Harrathd,
Jameel Al-Tamimid,
Ismail Özdemire,
Sedat Yaşare and
Naceur Hamdi*ab
aResearch Laboratory of Environmental Sciences and Technologies (LR16ES09), Higher Institute of Environmental Sciences and Technology, University of Carthage, Hammam-Lif, Tunisia. E-mail: naceur.hamdi@isste.rnu.tn; Fax: +966-6333-9351; Tel: +966-556-394-839
bChemistry Department, College of Science and Arts, Qassim University, Al-Rass, Kingdom of Saudi Arabia
cEcole Nationale Supérieure de Chimie de Lille, Unité de Catalyse et Chimie du Solide, UMR CNRS 8181, USTL, BP 90108, 59652 Villeneuve d’Ascq, France
dZoology Department, College of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia
eİnönü University, Faculty of Science and Art, Department of Chemistry, Malatya, Turkey
First published on 21st December 2018
Correction for ‘Efficient in situ N-heterocyclic carbene palladium(II) generated from Pd(OAc)2 catalysts for carbonylative Suzuki coupling reactions of arylboronic acids with 2-bromopyridine under inert conditions leading to unsymmetrical arylpyridine ketones: synthesis, characterization and cytotoxic activities’ by Nedra Touj et al., RSC Adv., 2018, 8, 40000–40015.
The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.
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