Randomized trial demonstrates an efficient method for synthesizing thioglycoside derivatives, indicating potential for biological applications.
This study presents an efficient approach for the di‐functionalization of 1,2,4‐triazoles with thiosugars, combining photochemical processes and metal‐catalyzed coupling reactions under mild conditions. Exploiting the dual reactivity of the selected 1,2,4‐triazoles, this strategy enables selective and versatile transformations, affording a new family of 1,2,4‐triazole derivatives conjugated with thiosugars with potential for further exploration in biologically relevant studies.
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Jaballah et al. (2026) studied this question.
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