Lei
Dong
a,
Yi
Zang
b,
Dan
Zhou
ab,
Xiao-Peng
He
*a,
Guo-Rong
Chen
a,
Tony D.
James
c and
Jia
Li
*b
aKey Laboratory for Advanced Materials & Institute of Fine Chemicals, East China University of Science and Technology, 130 Meilong Rd., Shanghai 200237, P. R. China. E-mail: xphe@ecust.edu.cn
bNational Center for Drug Screening, State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, 189 Guo Shoujing Rd., Shanghai 201203, P. R. China. E-mail: jli@simm.ac.cn
cDepartment of Chemistry, University of Bath, Bath, BA2 7AY, UK
First published on 7th July 2015
Correction for ‘Glycosylation enhances the aqueous sensitivity and lowers the cytotoxicity of a naphthalimide zinc ion fluorescence probe’ by Lei Dong et al., Chem. Commun., 2015, DOI: 10.1039/c5cc04357c.
“Click chemistry between an azido galactoside and glucoside with an alkynyl naphthalimide, followed by introduction of the DPA motif, produced triazole-linked galactosyl (DL1) and glucosyl (DL2) DPA-naphthalimides, respectively (Fig. 1a and ESI†)”.
The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.
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