Phenylacetylene (English Wikipedia)

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

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doi.org

  • Bordwell, F.G. (1988). "Equilibrium acidities in dimethyl sulfoxide solution". Acc. Chem. Res. 21: 456–463. doi:10.1021/ar00156a004.
  • Streitwieser, A. Jr.; Ruben, D.M.E (1971). "Acidity of hydrocarbons. XXXV. Equilibrium acidities of phenylacetylene and tert-butylacetylene in cyclohexylamine". J. Am. Chem. Soc. 93: 1794–1795. doi:10.1021/ja00736a045.
  • Kenneth N. Campbell, Barbara K. Campbell (1950). "Phenylacetylene". Organic Syntheses. 30: 72. doi:10.15227/orgsyn.030.0072.
  • John C. Hessler (1922). "Phenylacetylene". Organic Syntheses. 2: 67. doi:10.15227/orgsyn.002.0067.
  • Nwokogu, Godson C.; Zemolka, Saskia; Dehme, Florian (2007). "Trimethylsilylacetylene". EROS. doi:10.1002/047084289X.rt288.pub2. ISBN 978-0471936237.
  • Campbell, I. D.; Eglinton, G. (1965). "Diphenyldiacetylene". Organic Syntheses. 45: 39. doi:10.15227/orgsyn.045.0039.
  • Gerhard Hilt; Thomas Vogler; Wilfried Hess; Fabrizio Galbiati (2005). "A simple cobalt catalyst system for the efficient and regioselective cyclotrimerisation of alkynes". Chemical Communications. 2005 (11): 1474–1475. doi:10.1039/b417832g. PMID 15756340.
  • Ardizzoia, G. A.; Brenna, S.; Cenini, S.; LaMonica, G.; Masciocchi, N.; Maspero, A. (2003). "Oligomerization and Polymerization of Alkynes Catalyzed by Rhodium(I) Pyrazolate Complexes". Journal of Molecular Catalysis A: Chemical. 204–205: 333–340. doi:10.1016/S1381-1169(03)00315-7.

nih.gov

pubmed.ncbi.nlm.nih.gov