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Collect. Czech. Chem. Commun. 1988, 53, 301-307
https://doi.org/10.1135/cccc19880301

Structure of 5-nitro-2-methylbenzoic acid: ortho Effect of the methyl group

Bernard Tinanta, Jean-Paul Declercqa, Maurice Van Meersschea and Otto Exnerb

a Laboratoire de chimie physique et de cristallographie Université Catolique de Louvain, 1348 Louvain la Neuve, Belgium
b Institute of Organic Chemistry and Biochemistry Czechoslovak Academy of Sciences, 166 10 Prague 6, Czechoslovakia

Crossref Cited-by Linking

  • Hnyk Drahomír, Samdal Svein, Exner Otto, Wann Derek A., Rankin David W. H.: Does 2-Methylacetophenone Comply with Steric Inhibition of Resonance? A Direct Experimental Proof of Its Nonplanar Conformation from a Joint Ab Initio/Electron Diffraction Analysis. J. Org. Chem. 2010, 75, 4939. <https://doi.org/10.1021/jo100291r>
  • Kulhánek Jirií, Böhm Stanislav, Palát Karel, Exner Otto: Steric inhibition of resonance: revision of the principle on the electronic spectra of methyl‐substituted acetophenones. J of Physical Organic Chem 2004, 17, 686. <https://doi.org/10.1002/poc.750>
  • Fiedler Pavel, Exner Otto: Conformation of Aromatic Carbonyl Derivatives: An Infrared Study. Collect. Czech. Chem. Commun. 2004, 69, 797. <https://doi.org/10.1135/cccc20040797>
  • Otyepková Eva, Nevěčná Tat'jana, Kulhánek Jiří, Exner Otto: Ortho effect and steric inhibition of resonance: basicities of methyl‐substituted acetophenones. J of Physical Organic Chem 2003, 16, 721. <https://doi.org/10.1002/poc.642>
  • Císařová Ivana, Podlaha Jaroslav, Böhm Stanislav, Exner Otto: Steric Effects and Steric Inhibition of Resonance in Benzene Derivatives: 2,3-Dimethylbenzoic Acid. Collect. Czech. Chem. Commun. 2000, 65, 216. <https://doi.org/10.1135/cccc20000216>
  • Fiedler Pavel, Exner Otto: Infrared spectra and conformation of methyl-substituted benzoic acids. J Phys Org Chem 1998, 11, 141. <https://doi.org/10.1002/(SICI)1099-1395(199802)11:2<141::AID-POC982>3.0.CO;2-T>
  • Fiedler Pavel, Exner Otto: Infrared spectra and conformation of methyl-substituted benzoic acids. J. Phys. Org. Chem. 1998, 11, 141. <https://doi.org/10.1002/(SICI)1099-1395(199802)11:2<141::AID-POC982>3.0.CO;2-T>
  • Tinant Bernand, Declercq Jean‐Paul, VšEtečKa Václav, Exner Otto: Ortho, effect of one methyl group: Conformation of methyl 5‐nitro‐2‐methylbenzoate in crystal and in solution. J of Physical Organic Chem 1991, 4, 721. <https://doi.org/10.1002/poc.610041204>
  • Exner Otto, Hnyk Drahomír, Všetečka Václav: Dipole moments and electron distribution of acyl chlorides and acyl bromides. J of Physical Organic Chem 1989, 2, 476. <https://doi.org/10.1002/poc.610020606>
  • TINANT B., DECLERCQ J.‐P., VAN MEERSSCHE M., EXNER O.: ChemInform Abstract: Structure of 5‐Nitro‐2‐methylbenzoic Acid: ortho Effect of the Methyl Group. ChemInform 1988, 19. <https://doi.org/10.1002/chin.198823055>