Abstract
The electrochemical synthesis of aryl azoles was performed for the first time in a microflow reactor. The reaction relies on the anodic oxidation of the arene partners making these substrates susceptible for C-H functionalization with azoles, thus requiring no homogeneous transition-metal-based catalysts. The synthetic protocol benefits from the implementation of a microflow setup, leading to shorter residence times (10 min), compared to previously reported batch systems. Various azolated compounds (22 examples) are obtained in good to excellent yields.
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CITATION STYLE
Buglioni, L., Beslać, M., & Noël, T. (2021). Dehydrogenative Azolation of Arenes in a Microflow Electrochemical Reactor. Journal of Organic Chemistry, 86(22), 16195–16203. https://doi.org/10.1021/acs.joc.1c01409
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