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. 2020 Sep 25;8:580899. doi: 10.3389/fchem.2020.580899

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Copyright © 2020 Sikora, Zielonka, Dębowska, Michalski, Smulik-Izydorczyk, Pięta, Podsiadły, Artelska, Pierzchała and Kalyanaraman.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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Scheme 1 — (A) Oxidation of aryl boronates to phenolic products in the reaction with H₂O₂. (B–D) Reaction of H₂O₂ with molecular boronate probes: (B) p-dihydroxyborylbenzyloxycarbonyl derivative of 4-nitroaniline, (C) p-dihydroxyborylbenzyloxycarbonyl derivative of 7-amino-4-methylcoumarin, (D) diboronate derivative of fluorescein, PF1.