Tham khảo Cuban

  1. 1 2 3 Biegasiewicz, Kyle; Griffiths, Justin; Savage, G. Paul; Tsanakstidis, John; Priefer, Ronny (2015). "Cubane: 50 years later". Chemical Reviews. 115: 6719–6745. doi:10.1021/cr500523x. PMID 26102302.
  2. 1 2 Eaton, Philip E.; Cole, Thomas W. (1964). "Cubane". J. Am. Chem. Soc. 86 (15): 3157–3158. doi:10.1021/ja01069a041.
  3. ↑ Eaton, Philip E.; Cole, Thomas W. (1964). "The Cubane System". J. Am. Chem. Soc. 86 (5): 962–964. doi:10.1021/ja01059a072.
  4. ↑ Freedman, H. H. (1961). "Tetraphenylcyclobutadiene Derivatives. II.1 Chemical Evidence for the Triplet State". J. Am. Chem. Soc. 83 (9): 2195–2196. doi:10.1021/ja01470a037.
  5. ↑ Freedman, H. H.; Petersen, D. R. (1962). "Tetraphenylcyclobutadiene Derivatives. IV.1 "Octaphenylcubane"; A Dimer of Tetraphenylcyclobutadiene". J. Am. Chem. Soc. 84 (14): 2837–2838. doi:10.1021/ja00873a046.
  6. ↑ Pawley, G. S.; Lipscomb, W. N.; Freedman, H. H. (1964). "Structure of the Dimer of tetraphenylcyclobutadiene". J. Am. Chem. Soc. 86 (21): 4725–4726. doi:10.1021/ja01075a042.
  7. ↑ Pichierri, F. (2014). “Hypercubane: DFT-based prediction of an Oh-symmetric double-shell hydrocarbon”. Chem. Phys. Lett. 612: 198–202. doi:10.1016/j.cplett.2014.08.032.
  8. ↑ http://www.compchemhighlights.org/2014/12/hypercubane-dft-based-prediction-of-oh.html
  9. ↑ Eaton, Philip E.; Maggini, Michele (1988). “Cubene (1,2-dehydrocubane)”. J. Am. Chem. Soc. 110 (21): 7230–7232. doi:10.1021/ja00229a057.
  10. ↑ Minyaev, Ruslan M.; Minkin, Vladimir I.; Gribanova, Tatyana N. (2009). “2.3 A Theoretical Approach to the Study and Design of Prismane Systems”. Trong Dodziuk, Helena (biên tập). Strained Hydrocarbons. Wiley. tr. 55. ISBN 9783527627141.
  11. ↑ Smith, Michael B.; March, Jerry (2001). March’s Advanced Organic Chemistry (5th ed.). John Wiley & Sons. p. 1459. ISBN 0-471-58589-0.
  12. ↑ Kindler, K.; Lührs, K. (1966). "Studien über den Mechanismus chemischer Reaktionen, XXIII. Hydrierungen von Nitrilen unter Verwendung von Terpenen als Wasserstoffdonatoren". Chem. Ber. 99: 227–232. doi:10.1002/cber.19660990135.