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- W1649755909 endingPage "84" @default.
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- W1649755909 abstract "Aromatic compounds having oxygen-containing substituents such as phenols, phenyl ketones, benzyl alcohols, and benzoic acids undergo regioselective arylation and vinylation via C–H bond cleavage in the presence of transition-metal catalysts. The latter two substrates are also arylated and vinylated via C–C bond cleavage accompanied by liberation of ketones and CO2, respectively. Coordination of their anionic oxygen to the metal center is the key to activate the inert bonds effectively and regioselectively. The recent progress of these oxygen-directed reactions is summarized herein." @default.
- W1649755909 created "2016-06-24" @default.
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- W1649755909 date "2007-01-01" @default.
- W1649755909 modified "2023-10-11" @default.
- W1649755909 title "Catalytic Arylation and Vinylation Reactions Directed by Anionic Oxygen Functions via Cleavage of C – H and C – C Bonds" @default.
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- W1649755909 doi "https://doi.org/10.1007/3418_2007_066" @default.
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