The development of multifunctional bioorthogonal tools is essential for expanding their utility in biomedical research. Here, we report a gram-scale accessible building block, 3-(mesyloxyethyl)-6-(diethylphosphonomethyl)-tetrazine, featuring two orthogonal reactive handles. This scaffold enables the modular construction of a series of dual-conjugated tetrazine probes with versatile functionalities. Remarkably, the dual-conjugated architecture was found to induce bathochromic emission in the resulting bioorthogonal adducts, thereby facilitating new fluorophores in situ formation and offering a promising platform for the design of theranostic agents.
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Wang et al. (2025) studied this question.
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