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17O NMR studies on (E)-3-arylidenechromanone and -flavanone derivatives
Authors:Gábor Tóth  András Simon  Albert Lévai  Hanspeter Kählig  Hermann Kalchhauser
Affiliation:1. Technical Analytical Research Group of the Hungarian Academy of Sciences, Institute for General and Analytical Chemistry of the Budapest University of Technology and Economics, Szent Gellért tér 4, H-1111 Budapest, Hungary;2. Department of Organic Chemistry, Debrecen University, P.O.Box 20, H-4010 Debrecen, Hungary;3. Universität Wien, Institut für Organische Chemie, Währinger Str. 38, A-1090 Vienna, Austria
Abstract: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. Copyright © 2001 John Wiley & Sons, Ltd.
Keywords:NMR  13C NMR  17O NMR  (E)-3-arylidenechromanones  (E)-3-arylideneflavanones  substituent effects  Hammett σp+
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