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Determination of Dihydrobenzoacridinone Structures by NMR, IR, and UV Spectroscopy and Mass Spectrometry

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Journal of Applied Spectroscopy Aims and scope

Condensation of 2-naphthylamine, aromatic aldehydes, and dimedone was found to produce 9,10-dihydrobenzo[a] acridin-11-one derivatives according to PMR, 13C NMR, and IR spectroscopy and mass spectrometry. Correlation spectroscopy showed that the carbonyl in the synthesized dihydrobenzoacridinone derivatives was located on C11.

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Authors and Affiliations

  1. Institute of Physical Organic Chemistry, National Academy of Sciences of Belarus, 13 Surganov Str., Minsk, 22007, Belarus

    N. G. Kozlov, Yu. D. Zhiharko, E. D. Skakovsky, M. M. Ogorodnikova & L. I. Basalaeva

  2. Institute of Bioorganic Chemistry, National Academy of Sciences of Belarus, Minsk, Belarus

    A. V. Baranovsky

Authors
  1. N. G. Kozlov
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  2. Yu. D. Zhiharko
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  3. E. D. Skakovsky
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  4. A. V. Baranovsky
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  5. M. M. Ogorodnikova
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  6. L. I. Basalaeva
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Corresponding author

Correspondence to N. G. Kozlov.

Additional information

Translated from Zhurnal Prikladnoi Spektroskopii, Vol. 82, No. 6, pp. 836–840, November–December, 2015.

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Kozlov, N.G., Zhiharko, Y.D., Skakovsky, E.D. et al. Determination of Dihydrobenzoacridinone Structures by NMR, IR, and UV Spectroscopy and Mass Spectrometry. J Appl Spectrosc 82, 915–919 (2016). https://doi.org/10.1007/s10812-016-0204-6

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  • DOI: https://doi.org/10.1007/s10812-016-0204-6

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