Scope and Limitations of Boron Fluorescent Complexes from Stable Nitrile Oxides in ABPP Assays

Anthracenenitrile oxide undergoes 1,3-dipolar cycloaddition reactions with 1-substituted-4-(prop-2-yn-1- yloxy)benzene affording the expected isoxazoles in good yields and as single regioisomers. N−O Bond cleavage and boron complexation afforded the corresponding boron complexes, derivatized with either a triple bond for clickchemistry applications or an oxime group for nitrile oxide 1,3- dipolar cycloaddition. The optical properties of these compounds show potential for employment as fluorescent tags in imaging techniques. The activity-based protein profiling assays showed good reactivity for the synthesized probes even with short peptide chains (epoxomicin). Scope and limitations are discussed in the light of the obtained results.