Abstract
Photolysis of 3-iodo-4-methyl-7-diethylaminocoumarin in the presence of N-methylpyrrole, furan, thiophene, selenophene, pyridine, indole, imidazole, and benzimidazole results in the formation of a series of 3-hetaryl-7-aminocoumarins. The spectral luminescence characteristics of these newly synthesized compounds have been investigated.
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For communication 9, see [1].
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 11, pp. 1469–1473, November, 1990.
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Gordeeva, N.A., Kirpichënok, M.A. & Grandberg, I.I. Photochemical reactions of 7-aminocoumarins. 10. Reaction of 3-iodo-4-methyl-7-diethylaminocoumarin with heteroaromatic compounds. Chem Heterocycl Compd 26, 1222–1226 (1990). https://doi.org/10.1007/BF00476972
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DOI: https://doi.org/10.1007/BF00476972