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Despite extensive research in B–N-containing aromatic systems (most notably 1,2-azaborines) for their potential use in biomedicine and materials science, development of their oxygen counterparts, 1,2-oxaborines, remains underdeveloped. Presented herein is a straightforward route to access 1,2-oxaborines via a ring-closing metathesis strategy. Attempts to utilize the 1,2-oxaborine as a 1,3-diene in the Diels–Alder cycloaddition for potential application as a 4C + 1O synthon are also presented. Lastly, investigations regarding the aromaticity of the B–O heterocycles is probed using computations and isothermal reaction calorimetry.