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- W2022989689 abstract "We report an intermolecular hydroacylation of allylic alcohols with salicylaldehydes to afford β-hydroxy aryl ketones in 73–94% yields as single regioisomers. The reactivity and regioselectivity were promoted by catalytic amounts of a phosphinite that forms a dynamic covalent bond with the allylic alcohol. Hydroacylation of 1,2- and 1,1-disubstituted olefins generates β-hydroxy aryl ketones bearing tertiary and quaternary centers, respectively." @default.
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- W2022989689 date "2012-01-01" @default.
- W2022989689 modified "2023-09-25" @default.
- W2022989689 title "β-hydroxy ketones prepared by regioselective hydroacylation" @default.
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- W2022989689 doi "https://doi.org/10.1039/c1sc00634g" @default.
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