Nucleic acid aptamers have been employed to shield small molecules so that one among many similar reactive functional groups can be modified. This provides access to new chemical entities with potentially interesting properties while avoiding the use of covalent protecting groups.
References
Wuts, P. G. M. & Greene, T. W. Greene's Protective Groups in Organic Synthesis 4th edn (Wiley & Sons, 2006).
Young, I. S. & Baran, P. S. Nature Chem. 1, 193–205 10.1038/nchem.1402(2009).
Bastian, A. A., Marcozzi, A. & Herrmann, A. Nature Chem. 4, 789–793 10.1038/nchem.1402(2012).
Coquière, D., de la Lande, A., Parisel, O., Prangé, T. & Reinaud, O. Chem. Eur. J. 15, 11912–11917 (2009).
Cafeo, G., Kohnke, F. H. & Valenti, L. Tetrahedron Lett. 50, 4138–4140 (2009).
Grapsas, I., Massova, I. & Mobashery, S. Tetrahedron 54, 7705–7720 (1998).
Doudna, J. A. & Cech, T. R. Nature 418, 222–228 (2002).
Joyce, G. F. Angew. Chem. Int. Ed. 46, 6420–6436 (2007).
Breaker, R. R. Mol. Cell 43, 867–879 (2011).
Hermann, T. & Patel, D. J. Science 287, 820–825 (2000).
Alper, P. B., Hendrix, M., Sears, P. & Wong, C-H. J. Am. Chem. Soc. 120, 1965–1978 (1998).
Silverman, S. K. in Functional Nucleic Acids for Analytical Applications (eds Li, Y. & Lu, Y.) 47–108 (Springer Science & Business Media, LLC, 2009).
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Silverman, S. Shields for small molecules. Nature Chem 4, 774–775 (2012). https://doi.org/10.1038/nchem.1468
Published:
Issue Date:
DOI: https://doi.org/10.1038/nchem.1468
- Springer Nature Limited