Abstract
The corresponding 2-(o-hydroxystyryl)benzimidazoles were obtained by the condensation of aromatic o-hydroxyaldehydes with 5-nitro- and 5,6-dinitro-1,2,3-trimethylbenzimidazolium salts. It was established that derivatives of salicylaldehyde and 5-methoxysalicylaldehyde are capable of intramolecular cyclization in absolute, aprotic solvents to form spiro (benzimidazoline-2,2′-[2H]chromene) derivatives.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 7, pp. 961–966, July, 1971.
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Beresneva, N.K., Zakhs, É.R. & Éfros, L.S. Products of the condensation of 5-nitro- and 5,6-dinitro-1,2,3-trimethylbenzimidazolium salts with o-hydroxyaldehydes. Chem Heterocycl Compd 7, 897–902 (1971). https://doi.org/10.1007/BF00475721
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DOI: https://doi.org/10.1007/BF00475721