Matches in SemOpenAlex for { <https://semopenalex.org/work/W2766734385> ?p ?o ?g. }
- W2766734385 endingPage "6143" @default.
- W2766734385 startingPage "6140" @default.
- W2766734385 abstract "An N-bromosuccinimide-catalyzed intermolecular annulation of acetyl indoles with alkynes was developed, allowing for regioselective formation of valuable carbazoles through direct C-H bond functionalization. The readily available catalyst, wide substrate scope, gram scale synthesis, and mild conditions make this method practical. Mechanistic investigations indicate that the bromination of acetyl indole takes place to generate a bromide intermediate, followed by coupling with an alkyne and intramolecular cycloaromatization to furnish carbazole products." @default.
- W2766734385 created "2017-11-10" @default.
- W2766734385 creator A5007003411 @default.
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- W2766734385 creator A5080730614 @default.
- W2766734385 creator A5081944324 @default.
- W2766734385 creator A5084854649 @default.
- W2766734385 date "2017-11-02" @default.
- W2766734385 modified "2023-10-06" @default.
- W2766734385 title "<i>N</i>-Bromosuccinimide (NBS)-Catalyzed C–H Bond Functionalization: An Annulation of Alkynes with Electron Withdrawing Group (EWG)-Substituted Acetyl Indoles for the Synthesis of Carbazoles" @default.
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