17O NMR studies on (E)-3-arylidenechromanone and -flavanones derivatives

Gábor Tóth, András Simon, Albert Lévai, Hanspeter Kählig, Hermann Kalchhauser

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2 Citations (Scopus)


17O NMR data for some 3-arylidenechromanones and -flavanones are discussed in terms of mesomeric and steric substituent interactions. The transmission of long-range substituent effects was studied. 17O NMR chemical shifts were correlated with Hammett σp+ values for 4′-substituted derivatives.

Original languageEnglish
Pages (from-to)463-465
Number of pages3
JournalMagnetic Resonance in Chemistry
Issue number8
Publication statusPublished - Dec 1 2001



  • (E)-3-arylidenechromanones
  • (E)-3-arylideneflavanones
  • C NMR
  • Hammett σ
  • NMR
  • O NMR
  • Substituent effects

ASJC Scopus subject areas

  • Chemistry(all)
  • Materials Science(all)

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