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Developing efficient and selective methods for the divergent synthesis of spiro/fused cycles is of great interest yet poses a significant challenge. Herein, we present a distinctive approach for the divergent construction of pyrazole-fused medium-sized rings and pyrazolone spirocyclic frameworks. Unlike previous works that are limited to the construction of medium-sized rings, the presented strategy can achieve fused-to-spirocyclic framework conversion through an unprecedented asymmetric O - to C -acyl rearrangement of medium-sized ring systems. This approach is equally applicable to pharmaceutically relevant molecules, offering a versatile tool for late-stage modifications. Density functional theory calculations provide insights into the explanation for the regioselectivity of 1,4-acyl transfer, which has previously remained unexplored.
Xu et al. (Tue,) studied this question.