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- W2945591814 abstract "Abstract Transition‐metal‐catalyzed acetoxylation or hydroxylation of arene C−H bonds is regarded as a valuable transformation in organic synthesis for the efficient incorporation of oxygen atoms. [1] This mode of C−H oxidation has received much attention due to the important applications of phenol derivatives in natural products, pharmaceuticals, organic synthesis, metal ligands and materials science. Early discoveries for arene C−H oxidation were generally limited due to poor selectivity, low efficiency and harsh conditions. [3] Strategie that rely coordinating directing groups have enabled the direct oxidation of a specific arene C−H bond with high regioselectivity and efficiency. This methods generally employ palladium (II) or ruthenium (II) catalysts and PhI(OAc) 2 or other stoichiometric oxidants under acidic conditions (Scheme , 1a). Methods using other transition metals, such as a rhodium (III) catalyzed ortho ‐C−H acetoxylation or hydroxylation, have also been reported." @default.
- W2945591814 created "2019-05-29" @default.
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- W2945591814 date "2019-05-23" @default.
- W2945591814 modified "2023-10-16" @default.
- W2945591814 title "Cu‐Mediated C7 Acetoxylation of Indolines" @default.
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- W2945591814 doi "https://doi.org/10.1002/slct.201901170" @default.
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