Abstract
Indolo(2,1-a]isoquinoline was alkylated at C(11) under catalytic hydrogenation conditions over rhenium heptasulfide in a medium of various alcohols. It was shown that the alkylation occurs by an electrophilic substitution mechanism and the yield of the products increases with decreasing acidity of the alcohols.
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Communication 7, see [1]
Translated from Khimiya Geterotsikiicheskikh Soedinenii, No. 3, pp. 377–380, March, 1994.
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Soldatova, S.A., Alarkon, J.A., Mamyrbekova, Z.A. et al. Indolopyridines with a hetero atom at a position of fusion 8. Reductive C-alkylation of indolo[2,1-a]isoquinolone. Chem Heterocycl Compd 30, 331–334 (1994). https://doi.org/10.1007/BF01165700
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DOI: https://doi.org/10.1007/BF01165700