Open Access Article
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Correction: Enantiomeric NMR discrimination of carboxylic acids using actinomycin D as a chiral solvating agent
Liwen
Bai
,
Pian
Chen
,
Jiangxia
Xiang
,
Jiarui
Sun
and
Xinxiang
Lei
*
School of Pharmaceutical Sciences, South Central University for Nationalities, Wuhan, 430074, P.R. China. E-mail: xxlei@mail.scuec.edu.cn
First published on 28th March 2019
Abstract
Correction for ‘Enantiomeric NMR discrimination of carboxylic acids using actinomycin D as a chiral solvating agent’ by Liwen Bai, et al., Org. Biomol. Chem., 2019, 17, 1466–1470.
The authors regret that an incorrect structure for actinomycin D was included in Scheme 1, the graphical abstract and the ESI. The correct graphics are shown below.
 | ||
| Scheme 1 Chemical structures of Act-D (1), mandelic acid (2), 2-bromomandelic acid (3), 2-fluoromandelic acid (4), 4-chloromandelic acid (5), 4-bromomandelic acid (6), 4-fluoromandelic acid (7), 4-methoxymandelic acid (8), 3,5-difluoromandelic acid (9), α-methoxyphenylacetic acid (10), 2-naphthaleneacetic acid (11), 2-phthalimidopropionic acid (12), phenylsuccinic acid (13), 2-hydroxy-3-methylbutyric acid (14), and 2-hydroxycaprylic acid (15). | ||
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 2019 |