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Correction: Dithiolopyrrolones: biosynthesis, synthesis, and activity of a unique class of disulfide-containing antibiotics
Bo
Li
*a,
Walter J.
Wever
b,
Christopher T.
Walsh
c and
Albert A.
Bowers
*b
aDepartment of Chemistry, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599. E-mail: boli@email.unc.edu
bDivision of Chemical Biology and Medicinal Chemistry, Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599. E-mail: abower2@email.unc.edu
cDepartment of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, 200 Longwood Ave., Boston, MA 02115
First published on 19th January 2015
Abstract
Correction for ‘Dithiolopyrrolones: biosynthesis, synthesis, and activity of a unique class of disulfide-containing antibiotics’ by Bo Li et al., Nat. Prod. Rep., 2014, 31, 905–923.
There were several errors in the structures of thiomarinols as depicted in Fig. 1 of the review: the length of the fatty acyl chain was misannotated, as was the oxidation state at C-4 of Thiomarinol D. The stereochemistry at C-4, which was rigorously proven by H. Shiozawa and S. Takahashi, J. Antibiotics, 1994, 47, 851–853, was not included. In Scheme 1, the length of the fatty acyl chain in thiomarinol H and J was also misannotated. These errors have been rectified in the revised figures below.
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| Fig. 1 Structures of isolated dithiolopyrrolones. | ||
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| Scheme 1 Mutasynthetic preparation of thiomarinol derivatives. | ||
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 2015 |