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Ruthenium-Catalyzed Redox Isomerizations inside Living Cells

[Image: see text] Tailored ruthenium(IV) complexes can catalyze the isomerization of allylic alcohols into saturated carbonyl derivatives under physiologically relevant conditions, and even inside living mammalian cells. The reaction, which involves ruthenium-hydride intermediates, is bioorthogonal...

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Autores principales: Vidal, Cristian, Tomás-Gamasa, María, Gutiérrez-González, Alejandro, Mascareñas, José L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2019
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6497367/
https://www.ncbi.nlm.nih.gov/pubmed/30892889
http://dx.doi.org/10.1021/jacs.9b00837
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author Vidal, Cristian
Tomás-Gamasa, María
Gutiérrez-González, Alejandro
Mascareñas, José L.
author_facet Vidal, Cristian
Tomás-Gamasa, María
Gutiérrez-González, Alejandro
Mascareñas, José L.
author_sort Vidal, Cristian
collection PubMed
description [Image: see text] Tailored ruthenium(IV) complexes can catalyze the isomerization of allylic alcohols into saturated carbonyl derivatives under physiologically relevant conditions, and even inside living mammalian cells. The reaction, which involves ruthenium-hydride intermediates, is bioorthogonal and biocompatible, and can be used for the “in cellulo” generation of fluorescent and bioactive probes. Overall, our research reveals a novel metal-based tool for cellular intervention, and comes to further demonstrate the compatibility of organometallic mechanisms with the complex environment of cells.
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spelling pubmed-64973672019-05-03 Ruthenium-Catalyzed Redox Isomerizations inside Living Cells Vidal, Cristian Tomás-Gamasa, María Gutiérrez-González, Alejandro Mascareñas, José L. J Am Chem Soc [Image: see text] Tailored ruthenium(IV) complexes can catalyze the isomerization of allylic alcohols into saturated carbonyl derivatives under physiologically relevant conditions, and even inside living mammalian cells. The reaction, which involves ruthenium-hydride intermediates, is bioorthogonal and biocompatible, and can be used for the “in cellulo” generation of fluorescent and bioactive probes. Overall, our research reveals a novel metal-based tool for cellular intervention, and comes to further demonstrate the compatibility of organometallic mechanisms with the complex environment of cells. American Chemical Society 2019-03-20 2019-04-03 /pmc/articles/PMC6497367/ /pubmed/30892889 http://dx.doi.org/10.1021/jacs.9b00837 Text en Copyright © 2019 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes.
spellingShingle Vidal, Cristian
Tomás-Gamasa, María
Gutiérrez-González, Alejandro
Mascareñas, José L.
Ruthenium-Catalyzed Redox Isomerizations inside Living Cells
title Ruthenium-Catalyzed Redox Isomerizations inside Living Cells
title_full Ruthenium-Catalyzed Redox Isomerizations inside Living Cells
title_fullStr Ruthenium-Catalyzed Redox Isomerizations inside Living Cells
title_full_unstemmed Ruthenium-Catalyzed Redox Isomerizations inside Living Cells
title_short Ruthenium-Catalyzed Redox Isomerizations inside Living Cells
title_sort ruthenium-catalyzed redox isomerizations inside living cells
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6497367/
https://www.ncbi.nlm.nih.gov/pubmed/30892889
http://dx.doi.org/10.1021/jacs.9b00837
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