Crossref Cited-by Linking logo

Collect. Czech. Chem. Commun. 1965, 30, 355-379
https://doi.org/10.1135/cccc19650355

Physical properties and chemical reactivity of alternant hydrocarbons and related compounds. VIII. Quantum chemical reactivity indices of pyridine-like heterocycles

R. Zahradník and C. Párkányi

Crossref Cited-by Linking

  • Botti V., Elisei F., Faraguna F., Marinić Ž., Mazzucato U., Šagud I., Šindler-Kulyk M., Spalletti A.: Deactivating effect of the pyridine n,π* states on the photoreactivity of 5-[2-(pyrid-n-yl)ethenyl]oxazole (n= 2, 3 and 4). Journal of Photochemistry and Photobiology A: Chemistry 2016, 329, 262. <https://doi.org/10.1016/j.jphotochem.2016.07.009>
  • Spanget‐Larsen Jens: Structure–reactivity correlations for aza‐arenes. Proton affinities, pKa values, hydrogen–deuterium exchange rates and radical‐induced 13C shifts. J of Physical Organic Chem 1995, 8, 496. <https://doi.org/10.1002/poc.610080709>
  • Dr. Hess Doz. U., Huhn D.: Elektrochemische Adamantylierung von reduktiv dehalogenierbaren Chinolinen. J. Prakt. Chem. 1981, 323, 381. <https://doi.org/10.1002/prac.19813230305>
  • Párkányi Cyril, Herndon William C.: BOND LENGTHS AND BOND ORDERS IN π-ELECTRON HETEROCYCLES. Phosphorous and Sulfur and the Related Elements 1978, 4, 1. <https://doi.org/10.1080/03086647808079955>
  • Abramenko P. I., Kosobutskii V. A.: Electronic structures and reactivities of methyl-substituted thienothiazoles and thieno- and furopyridines. Chem Heterocycl Compd 1976, 12, 995. <https://doi.org/10.1007/BF00480390>
  • Veksler K. V., �fros L. S.: Reactivity of 4,9-diazapyrene. Chem Heterocycl Compd 1975, 11, 594. <https://doi.org/10.1007/BF00480487>
  • Almlöf J., Roos B., Wahlgren U., Johansen H.: The electronic structure of the azabenzenes an ab initio MO-SCF-LCAO study. Journal of Electron Spectroscopy and Related Phenomena 1973, 2, 51. <https://doi.org/10.1016/0368-2048(73)80048-9>
  • Reimlinger Hans, Gilles Jean‐Marie, Anthoine Gilbert, Vandewalle Jan J. M., Lingier Willy R. F., de Ruiter Ernest, Merényi Robert, Hubert André: Kondensierte Isochinoline, III Untersuchungen über die Reaktivität der s ‐Triazolo[3.4‐a]isochinoline. Chem. Ber. 1971, 104, 3925. <https://doi.org/10.1002/cber.19711041222>
  • Chalvet O., Daudel R., McKillop T.F.W.: Towards a unified theoretical treatment of the transition state in the reactions of unsaturated compounds—II. Tetrahedron 1970, 26, 349. <https://doi.org/10.1016/S0040-4020(01)97832-9>
  • Grabowska A., Pakuła B., Panciř J.: EXCITED STATES OF SIX‐MEMBERED N‐HETEROCYCLES. FLUORESCENCE, PHOSPHORESCENCE AND ACID‐BASE EQUILIBRIA OF FIVE MONO‐ AND DIAZA‐PHENANTHRENES IN THE LOWEST EXCITED (τ,τ) STATES. Photochem & Photobiology 1969, 10, 415. <https://doi.org/10.1111/j.1751-1097.1969.tb05706.x>
  • Foucart J., Nasielski J., Vander Donckt E.: Oxydation des Bases Monoaza‐Aromatiques Par L'Acide Perbenzoïque. Bulletin des Soc Chimique 1966, 75, 17. <https://doi.org/10.1002/bscb.19660750103>
  • Kuthan J., Skála V.: Über die Korrelation der NMR‐Protonenspektren mit Reaktivitätsindices einiger pyridinoider Heterocyclen. Zeitschrift fuer Chemie 1966, 6, 422. <https://doi.org/10.1002/zfch.19660061111>
  • Lynch Brian M., Dou Henri J.M.: Simple linear relationships between proton chemical shifts and calculated π-electron densities in nitrogen heterocycles. Tetrahedron Letters 1966, 7, 2627. <https://doi.org/10.1016/S0040-4039(01)84128-9>
  • Abramovitch R.A., Saha J.G.: Arylations using diazonium tetrafluoroborate and pyridine. Tetrahedron 1965, 21, 3297. <https://doi.org/10.1016/S0040-4020(01)96951-0>