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Benzenoid-quinone tautomerism in azomethines and their structural analogs. 34. 3-hydroxy-1-methylindole-2-carbaldehyde imines

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

N-aryl- and N-alkylimines of 3-hydroxy-1-methylindolecarbaldehyde have been synthesized, and have been assigned ketoenamino structures based on their UV, IR, and PMR spectra. The fluorescent properties of these materials have also been examined.

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For communication No. 33, see [1].

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 7, pp. 921–924, July, 1985.

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Sitkina, L.M., Dubonosov, A.D., Lyubarska, A.É. et al. Benzenoid-quinone tautomerism in azomethines and their structural analogs. 34. 3-hydroxy-1-methylindole-2-carbaldehyde imines. Chem Heterocycl Compd 21, 763–766 (1985). https://doi.org/10.1007/BF00519142

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  • DOI: https://doi.org/10.1007/BF00519142

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