Open Access Article
Soumi
Chakraborty
,
Arpan
Das
and
Swadhin K.
Mandal
*
Department of Chemical Sciences, Indian Institute of Science Education and Research (IISER) Kolkata, Mohanpur Campus, Pin-741246, Nadia, West Bengal, India. E-mail: swadhin.mandal@iiserkol.ac.in
First published on 14th December 2021
Correction for ‘Redox-active ligand based Mn(I)-catalyst for hydrosilylative ester reduction’ by Soumi Chakraborty et al., Chem. Commun., 2021, 57, 12671–12674, DOI: 10.1039/D1CC05614J.
“In addition, a few Mn-complexes were reported for silylative reduction of esters to alcohol although the mechanism was not well-explored.23–26 Except for a very recent report by Royo and coworkers,26 earlier protocols11,17–18,23–25 demanded the use of costly silanes such as phenylsilane and phosphine-based ligands, which are comparatively expensive and prone to degradation.27”
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