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- W2415143552 abstract "A palladium‐catalyzed ortho ‐directed alkylation of O ‐methyl ketoximes that proceeds through a regioselective ring‐opening reaction of epoxides has been demonstrated. This C(sp 2 )–H activation/alkylation protocol was carried out in pivalic acid/1,1,1,3,3,3‐hexafluoro‐2‐propanol (PivOH/HFIP, 2:8) as the solvent and was applied to various O ‐methyl ketoximes that contain either electron‐donating or electron‐withdrawing groups. Moreover, different types of epoxides were used in this alkylation reaction, which proceeded smoothly to give the corresponding products in moderate to good yields." @default.
- W2415143552 created "2016-06-24" @default.
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- W2415143552 date "2016-06-01" @default.
- W2415143552 modified "2023-10-16" @default.
- W2415143552 title "Palladium-Catalyzed C(sp2)-H Bond Alkylation of Ketoximes by Using the Ring-Opening of Epoxides" @default.
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- W2415143552 doi "https://doi.org/10.1002/ejoc.201600335" @default.
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