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- W2000176442 abstract "Deuterium and tritium labelling experiments show that the boron trifluoride-catalysed cyclisation of 4-(6-methoxy-indol-3-yl)butanol to 7-methoxytetrahydrocarbazole occurs by two simultaneous pathways. The major route involves initial cyclisation at the 3-position to give an intermediate spirocyclic indolenine salt which then rearranges to the tetrahydrocarbazole; the minor pathway involves direct attack at the 2-position. A similar duality of mechanism occurs in the solvolysis of the corresponding methoxyindolylbutyl tosylate." @default.
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- W2000176442 date "1973-01-01" @default.
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- W2000176442 title "Electrophilic substitution in indoles. Part VIII. The mechanism of electrophilic substitution in 6-methoxyindoles" @default.
- W2000176442 doi "https://doi.org/10.1039/p29730000872" @default.
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