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• W1934173202 endingPage "16386" @default.
• W1934173202 startingPage "16383" @default.
• W1934173202 abstract "Abstract A mild and convenient synthesis of carbazoles by TfOTMS (trimethylsilyl trifluoromethanesulfonate)‐catalyzed ring‐opening annulation of 2‐amidodihydrofurans is presented with a high degree of chemoselectivity and regioselectivity. This procedure was also scaled up to a gram‐scale synthesis. The reaction could involve an iminonium intermediate through a series of CO, CN bond cleavages, CC bond formations, and a 1,2‐migration process." @default.
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• W1934173202 date "2015-10-02" @default.
• W1934173202 modified "2023-10-14" @default.
• W1934173202 title "Facile Synthesis of Trisubstituted Carbazoles by Acid‐Catalyzed Ring‐Opening Annulation of 2‐Amidodihydrofurans with Indoles" @default.
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• W1934173202 doi "https://doi.org/10.1002/chem.201503260" @default.
• W1934173202 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/26428275" @default.
• W1934173202 hasPublicationYear "2015" @default.
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