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Pd(II)-Catalyzed Primary-C(sp3)–H Acyloxylation at Room Temperature

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Figshare2016-02-20 更新2026-04-29 收录
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https://figshare.com/articles/dataset/Pd_II_Catalyzed_Primary_C_sp_sup_3_sup_H_Acyloxylation_at_Room_Temperature/2503690
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With the aid of a novel S-methyl-S-2-pyridyl-sulfoximine (MPyS) directing group (DG), the unactivated primary β-C(sp3)–H bond of MPyS-N-amides oxidizes at room temperature. The catalytic conditions are applicable to the diacetoxylation of primary β,β′-C(sp3)–H bonds, and the carboxylic acid solvent is pivotal in the formation of the C–O bond. The MPyS-DG cleaves from the oxidation products and is recovered. This method provides convenient access to α,α′-disubstituted-β-hydroxycarboxylic acids.
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2016-02-20
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