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- W4239861008 abstract "In the presence of catalytic [Ru(p-cym)I2]2 and the base guanidine carbonate, benzoic acids react with internal alkynes to give the corresponding 2-vinylbenzoic acids. This alkyne hydroarylation is generally applicable to diversely substituted electron-rich and electron-poor benzoic and acrylic acids. Aryl(alkyl)acetylenes react regioselectively with formation of the alkyl-branched hydroarylation products, and propargylic alcohols are converted into γ-alkylidene-δ-lactones. The hydroarylation can also be conducted decarboxylatively with a different choice of catalyst and reaction conditions. This reaction variant, which does not proceed via intermediate formation of 2-vinylbenzoic acids, opens up a regioselective, waste-minimized synthetic entry to vinylarenes." @default.
- W4239861008 created "2022-05-12" @default.
- W4239861008 creator A5005364099 @default.
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- W4239861008 date "2016-04-26" @default.
- W4239861008 modified "2023-10-17" @default.
- W4239861008 title "Regioselective C−H Hydroarylation of Internal Alkynes with Arenecarboxylates: Carboxylates as Deciduous Directing Groups" @default.
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- W4239861008 doi "https://doi.org/10.1002/ange.201600894" @default.
- W4239861008 hasPublicationYear "2016" @default.
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