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Diastereodivergent Construction of Bicyclic γ‑Lactones via Enantioselective Ketone Hydroacylation

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NIAID Data Ecosystem2026-03-09 收录
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We present a diastereodivergent strategy for constructing bicyclic γ-lactones bearing quaternary carbon centers via ketone hydroacylation. By applying a Rh catalyst and JoSPOphos ligand, either the anti or syn bicyclic γ-lactones can be accessed with high enantio- and diastereoselectivities, depending on the choice of solvent, temperature, and counterion.

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2016-09-15
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