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• W2319253231 abstract "Activation of C2 and C3 of indoles by molecular iodine (I2) and base followed by in situ reaction with 1-(2-tosylaminophenyl)ketones or 2-tosylaminobenzaldehyde can afford highly substituted indolo(2,3-b)quinolines in moderate to excellent yields (up to 99%). The reaction provides a metal-free selective difunctionalization of indoles. The synthetic potential of the protocol has been illustrated by the synthesis of neocryptolepine and its 11-methyl analogue." @default.
• W2319253231 created "2016-06-24" @default.
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• W2319253231 date "2011-12-13" @default.
• W2319253231 modified "2023-09-30" @default.
• W2319253231 title "One-Pot Access to Indolo[2,3-<i>b</i>]quinolines by Electrophile-Triggered Cross-Amination/Friedel–Crafts Alkylation of Indoles with 1-(2-Tosylaminophenyl)ketones" @default.
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• W2319253231 doi "https://doi.org/10.1021/jo202035p" @default.
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