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Correction: Click activated protodrugs against cancer increase the therapeutic potential of chemotherapy through local capture and activation
Kui
Wu
a,
Nathan A.
Yee
b,
Sangeetha
Srinivasan
b,
Amir
Mahmoodi
b,
Michael
Zakharian
b,
Jose M.
Mejia Oneto
*b and
Maksim
Royzen
*a
aUniversity at Albany, SUNY, 1400 Washington Ave., LS-1136, Albany, NY 12222, USA. E-mail: mroyzen@albany.edu
bShasqi, Inc., 665 3rd St., Suite 501, San Francisco, CA 94107, USA. E-mail: jose@shasqi.com
First published on 21st May 2021
Abstract
Correction for ‘Click activated protodrugs against cancer increase the therapeutic potential of chemotherapy through local capture and activation’ by Kui Wu et al., Chem. Sci., 2021, 12, 1259–1271, DOI: 10.1039/D0SC06099B.
The authors regret that the reference to the bond-breaking bioorthogonal chemistry, termed ‘click-to-release’ was omitted from the original article. In addition, we would like to include a reference describing the synthesis of compound 1, which is an intermediate to the protodrugs described in the original article. These references are listed below as ref. 1 and 2.
The Royal Society of Chemistry apologizes for these errors and any consequent inconvenience to authors and readers.
References
- R. M. Versteegen, R. Rossin, W. ten Hoeve, H. M. Janssen and M. S. Robillard, Angew. Chem., Int. Ed., 2013, 52, 14112–14116 CrossRef CAS PubMed.
- R. Rossin, S. M. J. van Duijnhoven, W. ten Hoeve, H. M. Janssen, L. H. J. Kleijn, F. J. M. Hoeben, R. M. Versteegen and M. S. Robillard, Bioconjugate Chem., 2016, 27, 1697–1706 CrossRef CAS PubMed.
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