Abstract
5-Acyl-6-substituted 5,6-dihydrophenanthridines are formed in the reaction of phenanthridine with nucleophilic organic compounds in the presence of alkyl halides. This method made it possible to introduce a phenanthridine residue into the ring of dialkylanilines, 1-alkyl-1,2,3,4-tetrahydroquinolines, 1-alkylindolines, 2-alkylindoles, pyrroles, indoline, and α-methylfuran, and also made it possible to obtain several ketones of the phenanthridine series.
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See [1] for communication XVII.
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No, 5, pp. 669–672, May, 1972
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Sheinkman, A.K., Kucherenko, A.P. & Baranov, S.N. Reactions of cyclammonium cations. Chem Heterocycl Compd 8, 607–610 (1972). https://doi.org/10.1007/BF00488157
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DOI: https://doi.org/10.1007/BF00488157