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Synthesis of 2,2'-Quinocyanines with Long N-Alkyl Substituents

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

2,2'-Quinocyanines with long alkyl substituents on one or both nitrogen atoms have been synthesized. 1H NMR spectroscopy has been used to study the processes occurring during the alkylation of the starting quinoline bases.

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Authors and Affiliations

  1. N. N. Vorozhtsov Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, 630090, Russia

    N. A. Orlova, E. F. Kolchina, F. A Zhuravlev, M. M. Shakirov, T. N. Gerasimova & V. V. Shelkovnikov

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  1. N. A. Orlova
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  2. E. F. Kolchina
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  3. F. A Zhuravlev
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  4. M. M. Shakirov
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  5. T. N. Gerasimova
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  6. V. V. Shelkovnikov
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Orlova, N.A., Kolchina, E.F., Zhuravlev, F.A. et al. Synthesis of 2,2'-Quinocyanines with Long N-Alkyl Substituents. Chemistry of Heterocyclic Compounds 38, 1233–1241 (2002). https://doi.org/10.1023/A:1021785630927

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