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- W2180210596 abstract "Abstract The development of bioorthogonal reactions has classically focused on bond‐forming ligation reactions. In this report, we seek to expand the functional repertoire of such transformations by introducing a new bond‐cleaving reaction between N ‐oxide and boron reagents. The reaction features a large dynamic range of reactivity, showcasing second‐order rate constants as high as 2.3×10 3 M −1 s −1 using diboron reaction partners. Diboron reagents display minimal cell toxicity at millimolar concentrations, penetrate cell membranes, and effectively reduce N ‐oxides inside mammalian cells. This new bioorthogonal process based on miniscule components is thus well‐suited for activating molecules within cells under chemical control. Furthermore, we demonstrate that the metabolic diversity of nature enables the use of naturally occurring functional groups that display inherent biocompatibility alongside abiotic components for organism‐specific applications." @default.
- W2180210596 created "2016-06-24" @default.
- W2180210596 creator A5057797551 @default.
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- W2180210596 date "2015-11-16" @default.
- W2180210596 modified "2023-10-16" @default.
- W2180210596 title "A Bioorthogonal Reaction of <i>N</i>‐Oxide and Boron Reagents" @default.
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- W2180210596 doi "https://doi.org/10.1002/anie.201508861" @default.
- W2180210596 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4715665" @default.
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