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Journal of Molecular StructureVolume 267, Issue C, March 1992, Pages 411-414

Substituent efects on the carbon-13 chemical shifts in α-phenylpyridylacrylic acids(Article)

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  • aFaculty of Technology and Metallurgy, University of Belgrade, P.O. Box 494, YU-11001 Belgrade
  • bFaculty of Science, University of Belgrade, P.O. Box 550, YU-11001 Belgrade
  • cFaculty of Science, University of Novi Sad, YU-21000 Novi Sad

Abstract

The 13C N.M.R. spectra of some substituted α-phenylpyridylacrylic acids, α-phenyl, α-(3-pyrydyl) and α-(3-pyrydyl-N-oxide) cinnamic acids were determined in deuterated dimethyl sulfoxide (d6-DMSO). It has been shown that the subsitutent chemical shifts (SCS) for Cβatom ethylenic bond of the examined compounds correlated linearely with the summ of the corresponding substituent constants in the both rings (σx + σY). This correlation was interpreted as evidence that the electronic effects of both substituents are involved in conjugated aromatic system. © 1992.

  • ISSN: 00222860
  • CODEN: JMOSB
  • Source Type: Journal
  • Original language: English
  • DOI: 10.1016/0022-2860(92)87065-4
  • Document Type: Article

  Jovanović, B.Ž.; Faculty of Technology and Metallurgy, University of Belgrade, P.O. Box 494,
© Copyright 2014 Elsevier B.V., All rights reserved.

Cited by 1 document

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Enantioselective hydrogenation of propenoic acids bearing heteroaromatic substituents over cinchonidine modified Pd/alumina
(2009) Catalysis Communications
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