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- W2971128826 abstract "Manganese(II) chloride-catalyzed acetylation of alcohols, phenols thiols and amines with acetic anhydride is reported. This method is environment-friendly and economically viable as it involves inexpensive, relatively benign catalyst, mild reaction condition, and simple workup. Acetylation is performed under the solvent-free condition at ambient temperature and acetylated products obtained in good to excellent yields. Primary, secondary heterocyclic amines, and phenols with various functional groups are smoothly acetylated in good yields. This method exhibits exquisite chemoselectivity, the amino group is preferentially acetylated in the presence of a hydroxyl/thiol group." @default.
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- W2971128826 date "2019-08-28" @default.
- W2971128826 modified "2023-09-26" @default.
- W2971128826 title "Manganese-mediated acetylation of alcohols, phenols, thiols, and amines utilizing acetic anhydride" @default.
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- W2971128826 doi "https://doi.org/10.1080/00397911.2019.1650282" @default.
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