Abstract
The reduction of oximes of 3-hydroxyacetylindole, 3-benzyloxyacetylindole, and 3-ethoxy-acetylindole (mixtures of syn and anti isomers) gave α-(3-indolyl-β-hydroxyethylamine, α-(3-indolyl)-β-benzyloxyethylamine, and α-(3-indolyl)-β-ethoxyethylamine, the structures of which were confirmed by PMR and mass spectrometry.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 6, pp. 778–781, June, 1971.
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Preobrazhenskaya, M.N., Zhirnova, K.G., Kostyuchenko, N.P. et al. α-(3-Indolyl)-β-hydroxyethylamine and its derivatives. Chem Heterocycl Compd 7, 725–728 (1971). https://doi.org/10.1007/BF00476819
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DOI: https://doi.org/10.1007/BF00476819