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Correction: Masking thiol reactivity with thioamide, thiourea, and thiocarbamate-based MBPs
Hyeonglim
Seo
,
Alysia J.
Kohlbrand
,
Ryjul W.
Stokes
,
Jeewon
Chung
and
Seth M.
Cohen
*
Department of Chemistry and Biochemistry, University of California, San Diego, 9500 Gilman Drive, La Jolla, CA 92093, USA. E-mail: scohen@ucsd.edu
First published on 13th March 2023
Abstract
Correction for ‘Masking thiol reactivity with thioamide, thiourea, and thiocarbamate-based MBPs’ by Hyeonglim Seo et al., Chem. Commun., 2023, 59, 2283–2286, https://doi.org/10.1039/D2CC06596G.
The authors regret that in Fig. 1 of the original article the methyl-group of L-cysteine methyl ester (13) is incorrectly drawn. The corrected figure is shown here.
 | ||
| Fig. 1 Thioamide, thiourea, and thiocarbamate MBPs proposed for use in Zn(II)-dependent metalloenzymes. Compounds 9 and 10 were utilized as known thione-based MBPs and 2-mercaptophenol (11), captopril (12), and L-cysteine methyl ester (13) were used as representative thiol-based compounds in this paper. | ||
The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.
| This journal is © The Royal Society of Chemistry 2023 |