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• W3033186329 endingPage "152109" @default.
• W3033186329 startingPage "152109" @default.
• W3033186329 abstract "A practical and scalable approach for the synthesis of 3-substituted indoles is delineated via hydride nucleophilic addition to 3-substituted-2-oxindoles. The reaction proceeds through reductive aromatization involving indolinium ion intermediate. A wide range of 3-functionalized indoles have been synthesized. The method is employed for the synthesis of 3,3ʹ-bis-indoles and a dimeric 3-indole derivative. Moreover, this protocol is used to obtain naturally occuring amino acid tryptamine." @default.
• W3033186329 created "2020-06-12" @default.
• W3033186329 creator A5005828640 @default.
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• W3033186329 date "2020-07-01" @default.
• W3033186329 modified "2023-10-13" @default.
• W3033186329 title "Reductive aromatization of oxindoles to 3-substituted indoles" @default.
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• W3033186329 doi "https://doi.org/10.1016/j.tetlet.2020.152109" @default.
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