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Directed, Palladium(II)-Catalyzed Intermolecular Aminohydroxylation of Alkenes Using a Mild Oxidation System

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NIAID Data Ecosystem2026-03-10 收录
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https://figshare.com/articles/dataset/Directed_Palladium_II_-Catalyzed_Intermolecular_Aminohydroxylation_of_Alkenes_Using_a_Mild_Oxidation_System/6473132
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A palladium­(II)-catalyzed β,γ-aminohydroxylation reaction of nonconjugated alkenyl carbonyl compounds has been developed. This reaction utilizes a cleavable bidentate directing group to achieve regioselective aminopalladation. The resulting chelation-stabilized alkylpalladium­(II) intermediate is then hydroxylated using oxygen/2,6-dimethyl­benzoquinone in HFIP as the mild oxidation system. Under the optimized conditions, various nucleophiles and alkene substrates are capable of delivering good yields and high diastereoselectivities of the aminohydroxylated products.
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2018-06-12
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