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- W2150252712 abstract "3-Arylamino-2-formylindoles were converted into oximes and then acetylated to give the corresponding O-acetyl derivatives. Chloroacetylation of the latter was accompanied by elimination of acetic acid, yielding 3-(N-aryl-N-chloroacetyl)amino-2-cyanoindoles. When heated in pyridine, these nitriles underwent cyclization into novel δ-carboline derivatives: 4-amino-1-aryl-2-oxo-1,2-dihydropyrido[3,2-b]indol-3-yl)pyridinium chlorides. The structures of the compounds obtained were proved by IR and 1H NMR spectroscopy and mass spectrometry." @default.
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- W2150252712 date "2007-04-17" @default.
- W2150252712 modified "2023-09-24" @default.
- W2150252712 title "Synthesis of 4-Aminopyrido[3,2-b]indole Derivatives." @default.
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- W2150252712 doi "https://doi.org/10.1002/chin.200716142" @default.
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