Abstract
It is shown that 9-formyljulolidine reacts with phosphorus oxychloride with splitting out of the formyl group to give a symmetrical diphenylmethane dye. A comparison of data from the absorption spectra of polymethine dyes that are derivatives of dimethylaniline and julolidine indicates that the latter has greater electron-donor character.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 4, pp. 450–452, April, 1982.
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Mikhailenko, F.A., Balina, L.V. Polymethine dyes — julolidine derivatives. Chem Heterocycl Compd 18, 334–336 (1982). https://doi.org/10.1007/BF00503544
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DOI: https://doi.org/10.1007/BF00503544