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- W2951928492 abstract "Various N-propargylanilines bearing a conjugated diyne moiety at the 2-position were converted to tetracyclic fused carbazoles by treatment with a homogeneous gold(I) catalyst. This cascade reaction proceeds through indole formation with concomitant rearrangement of the N-propargyl group, intramolecular nucleophilic addition toward the resulting allene moiety, and subsequent hydroalkenylation. This transformation enables a one-pot synthesis of fused carbazoles from readily accessible substrates with 100% atom economy." @default.
- W2951928492 created "2019-06-27" @default.
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- W2951928492 date "2016-04-01" @default.
- W2951928492 modified "2023-09-25" @default.
- W2951928492 title "ChemInform Abstract: Synthesis of Fused Carbazoles by Gold-Catalyzed Tricyclization of Conjugated Diynes via Rearrangement of an N-Propargyl Group." @default.
- W2951928492 cites W2400611782 @default.
- W2951928492 doi "https://doi.org/10.1002/chin.201619112" @default.
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