Pentalene (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Pentalene" in English language version.

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doi.org

  • International Union of Pure and Applied Chemistry (2014). Nomenclature of Organic Chemistry: IUPAC Recommendations and Preferred Names 2013. The Royal Society of Chemistry. p. 209. doi:10.1039/9781849733069. ISBN 978-0-85404-182-4.
  • Hopf, Henning (2013). "Pentalenes-From Highly Reactive Antiaromatics to Substrates for Material Science". Angewandte Chemie International Edition. 52 (47): 12224–6. doi:10.1002/anie.201307162. PMID 24127399.
  • Bally T.; Chai S.; Neuenschwander M.; Zhu Z. (1997). "Pentalene: Formation, Electronic, and Vibrational Structure" (PDF). J. Am. Chem. Soc. 119 (8): 1869–1875(7). doi:10.1021/ja963439t. Archived from the original (reprint) on 2007-03-15. Retrieved 2007-07-06.
  • Hafner, K.; Süss, H. U. (1973). "1,3,5-Tri-tert-Butylpentalene. A Stabilized Planar 8π-Electron System". Angew. Chem. Int. Ed. Engl. 12 (7): 575–577. doi:10.1002/anie.197305751.
  • Katz, Thomas J.; Rosenberger, Michael. (1962). "The Pentalenyl Dianion". Journal of the American Chemical Society. 84 (5): 865. doi:10.1021/ja00864a038.
  • Summerscales, Owen T.; Cloke, F. Geoffrey N. (2006). "The organometallic chemistry of pentalene". Coordination Chemistry Reviews. 250 (9–10): 1122. doi:10.1016/j.ccr.2005.11.020.

nih.gov

pubmed.ncbi.nlm.nih.gov

  • Hopf, Henning (2013). "Pentalenes-From Highly Reactive Antiaromatics to Substrates for Material Science". Angewandte Chemie International Edition. 52 (47): 12224–6. doi:10.1002/anie.201307162. PMID 24127399.

unifr.ch

www-chem.unifr.ch

web.archive.org