Abdeslem Bouzina,
Billel Belhani,
Nour-Eddine Aouf and
Malika Berredjem*
Laboratory of Applied Organic Chemistry, Synthesis of Biomolecules and Molecular Modelling Group, Sciences Faculty, Chemistry Department, Badji-Mokhtar – Annaba University, Box 12, 23000 Annaba, Algeria. E-mail: malika.berredjem@univ-annaba.org
First published on 18th May 2017
Correction for ‘A novel, rapid and green method of phosphorylation under ultrasound irradiation and catalyst free conditions’ by Abdeslem Bouzina et al., RSC Adv., 2015, 5, 46272–46275.
The 1H-NMR, 13C-NMR and 31P-NMR spectra shown in the ESI for (S)-methyl-2-(2-(diethoxyphosphoryl)acetamido)-4-methylpentanoate and (S)-diethyl-(2-((1-hydroxy-4-methylpentan-2-yl)amino)-2-oxoethyl)phosphonate have been reproduced from ref. 1.
The 1H-NMR spectra for N-phenyl-(1-(2-dimethoxyphosphoryl)acetamide)sulfamide, N-3-fluorophenyl-(1-(2-dimethoxyphosphoryl)acetamide)sulfamide and N-4-methoxyphenyl-(1-(2-dimethoxyphosphoryl)acetamide)sulfamide have been reproduced from ref. 2.
These spectra were reproduced in this RSC Advances article for information purposes only. The product identities for the particular reactions reported in this RSC Advances article were confirmed by thin layer chromatography (TLC) and melting point analysis.
The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.
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