Intracellular deprotection reactions mediated by palladium complexes equipped with designed phosphine ligands
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American Chemical Society
Abstract
Discrete palladium(II) complexes featuring purposely designed phosphine ligands can promote depropargylation and deallylation reactions in cell lysates. These complexes perform better than other palladium sources, which apparently are rapidly deactivated in such hostile complex media. This good balance between reactivity and stability allows the use of these discrete phosphine palladium complexes in living mammalian cells, whereby they can mediate similar transformations. The presence of a phosphine ligand in the coordination sphere of palladium also provides for the introduction of targeting groups, such as hydrophobic phosphonium moieties, which facilitate the accumulation of the complexes in mitochondria
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Martínez-Calvo, M., Couceiro, J., Destito, P., Rodríguez, J., Mosquera, J., & Mascareñas, J. (2018). Intracellular Deprotection Reactions Mediated by Palladium Complexes Equipped with Designed Phosphine Ligands. ACS Catalysis, 6055-6061. doi: 10.1021/acscatal.8b01606
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https://doi.org/10.1021/acscatal.8b01606Sponsors
We are thankful for the financial support from the Xunta de Galicia (Centro Singular de Investigación de Galicia Acreditación 2016–2019, ED431G/09) and the European Union (European Regional Development Fund–ERDF). We also thank support given by the Spanish Grant No. SAF2016-76689-R, the Xunta de Galicia (Grant Nos. 2015-CP082, ED431C 2017/19), and the European Research Council (Advanced Grant No. 340055). M.M.C. thanks the Ministerio de Economía y Competitividad for the Postdoctoral fellowship (No. IJCI-2014-19326). J.R. and J.M. thank Xunta de Galicia and Ministerio of Educacion, respectively, for predoctoral fellowships. The authors thank R. Menaya-Vargas for technical assistance
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© 2018 American Chemical Society. This is an open access article published under an ACS AuthorChoice License (https://pubs.acs.org/page/policy/authorchoice_termsofuse.html), which permits copying and redistribution of the article or any adaptations for non-commercial purposes








