Explores a copper-catalyzed method to synthesize pyrrolo[1,2-a]pyrimidinone, suggesting efficient functionalization techniques.
A copper‐catalyzed annulation of oxime acetates with pyrrole scaffolds bearing α , β ‐unsaturated carbonyl groups was developed for the construction of pyrrolo[1,2‐ a ]pyrimidinone scaffolds. The key steps in this cascade process include a [3 + 2] spiroannulation, in situ oxidation, followed by rearrangement.
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Reddy et al. (2026) studied this question.
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