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- W2897545069 endingPage "10894" @default.
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- W2897545069 abstract "The organocatalyzed asymmetric dearomative addition of phenols to indol-2-ones generated in situ from 3-bromooxindoles was reported. This methodology leads to the efficient construction of a series of enantioenriched 3,3′-disubstituted oxindoles bearing vicinal all-carbon quaternary stereocenters via a dearomatization process of phenols under mild reaction conditions. Additionally, the representative large-scale reactions and related transformations of the dearomatized products reveal the potential synthetic utility of this protocol." @default.
- W2897545069 created "2018-10-26" @default.
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- W2897545069 date "2018-10-22" @default.
- W2897545069 modified "2023-10-15" @default.
- W2897545069 title "Construction of Vicinal All-Carbon Quaternary Stereocenters Enabled by a Catalytic Asymmetric Dearomatization Reaction of β-Naphthols with 3-Bromooxindoles" @default.
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- W2897545069 doi "https://doi.org/10.1021/acscatal.8b03905" @default.
- W2897545069 hasPublicationYear "2018" @default.
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