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. 2022 Apr 18;55(9):1324–1336. doi: 10.1021/acs.accounts.2c00113

Figure 1.

Figure 1

(A) Overarching kinetic model (pathways i–v) for pH-mediated speciation and protodeboronation. (B) Example pH–rate profiles for the protodeboronation of selected (hetero)arylboronic acids (50 mM, 50% vol. aq. dioxane, 70 °C). (C) Modified Swain–Lupton analysis of the protodeboronation of arylboronic acids. (D) Competing direct and indirect protodeboronation of boronate esters. Data from refs (1), (2), and (30).