Cuban (German Wikipedia)

Analysis of information sources in references of the Wikipedia article "Cuban" in German language version.

Last modified:

Ref.Un. Ref.Website
Global rank German rank
2nd place
3rd place
2,800th place
167th place
5th place
7th place

doi.org (Global: 2nd place; German: 3rd place)

  • L. Hedberg, K. Hedberg, E. P. E Kenneth, N. Nodari, A. G. Robiette: Bond lengths and quadratic force field for cubane. In: J. Am. Chem. Soc. 113, 1991, S. 1514–1517, doi:10.1021/ja00005a007.
  • P. E. Eaton: Cubane: Ausgangsverbindungen für die Chemie der 1990er Jahre und des nächsten Jahrhunderts. In: Angew. Chem., 104, 1992, S. 1447–1462, doi:10.1002/ange.19921041105.
  • P. E. Eaton, T. W. Cole: Cubane. In: J. Am. Chem. Soc. 86 1964, S. 3157–3158, doi:10.1021/ja01069a041.
  • P. E. Eaton, T. W. Cole: The Cubane System. In: J. Am. Chem. Soc. 86, 1964, S. 962–964, doi:10.1021/ja01059a072.
  • N. B. Chapman, J. M. Key, K. J. Toyne: The Preparation and Properties of Cage Polycyclic Systems – I. Pentacyclo[5.3.0.02,5.03,9.04,8]decane and Pentacyclo[4.3.0.02,5.03,8.04,7]nonane Derivatives. In: J. Org. Chem. 35, 1970, S. 3860–3867. doi:10.1021/jo00836a062.
  • Diego E. Collin, Edward H. Jackman, Nicolas Jouandon, Wei Sun, Mark E. Light, David C. Harrowven, Bruno Linclau: Decagram Synthesis of Dimethyl 1,4-Cubanedicarboxylate Using Continuous-Flow Photochemistry. In: Synthesis. Band 53, Nr. 07, April 2021, S. 1307–1314, doi:10.1055/s-0040-1705964.
  • Michael J. Falkiner, Stuart W. Littler, Kenneth J. McRae, G. Paul Savage, John Tsanaktsidis: Pilot-Scale Production of Dimethyl 1,4-Cubanedicarboxylate. In: Organic Process Research & Development. Band 17, Nr. 12, 20. Dezember 2013, S. 1503–1509, doi:10.1021/op400181g.
  • D. H. R. Barton, D. Crich, W. B. Motherwell: New and improved methods for the radical decarboxylation of acids. In: J. Chem. Soc., Chem. Commun. 1983, S. 939–941, doi:10.1039/C39830000939.
  • Sohan Lal, Argha Bhattacharjee, Arindrajit Chowdhury, Neeraj Kumbhakarna, Irishi N. N. Namboothiri: Approaches to 1,4‐Disubstituted Cubane Derivatives as Energetic Materials: Design, Theoretical Studies and Synthesis. In: Chemistry – An Asian Journal. Band 17, Nr. 17, September 2022, S. e202200489, doi:10.1002/asia.202200489.
  • M. A. White, R. E. Wasylishen, P. E. Eaton, Y. Xiong, K. Pramod, N. Nodari: Orientational Disorder in Solid Cubane: A Thermodynamic and 13C NMR Study. In: J. Phys. Chem., 96, Nr. 1, 1992, S. 421–425, doi:10.1021/j100180a078.
  • B. D. Kybett, S. Carroll, P. Natalis, D. W. Bonnell, J. L. Margrave, J. L. Franklin: Thermodynamic Properties of Cubane. In: J. Am. Chem. Soc., 88, 1966, S. 626–626, doi:10.1021/ja00955a056.
  • E. B. Fleischer: X-Ray Structure Determination of Cubane. In: J. Am. Chem. Soc., 86, 1964, S. 3889–3890, doi:10.1021/ja01072a069.
  • Fritz Vögtle: Reizvolle Moleküle der Organischen Chemie (= Teubner Studienbücher Chemie). Vieweg+Teubner Verlag, Wiesbaden 1989, ISBN 978-3-519-03503-9, doi:10.1007/978-3-322-96705-3.
  • N. L. Allinger, P. E. Eaton: The geometries of pentaprismane and hexaprismane insights from molecular mechanics. In: Tetrahedron Lett., 24, 1983, S. 3697–3700, doi:10.1016/S0040-4039(00)94512-X.
  • N. L. Allinger: Conformational Analysis. 130. MM2. A Hydrocarbon Force Field Utilizing V1 and V2 Torsional Terms. In: J. Am. Chem. Soc., 99, 1977, S. 8127–8134, doi:10.1021/ja00467a001.
  • H.-D. Martin, T. Urbanek, P. Pföhler, R. Walsh: The pyrolysis of cubane; an example of a thermally induced hot molecule reaction. In: J. Chem. Soc., Chem. Commun., 1985, S. 964–965, doi:10.1039/C39850000964.
  • P. E. Eaton, L. Cassar, J. Halpern: Silver(I)- and Palladium(II)-Catalyzed Isomerizations of Cubane. Synthesis and Characterization of Cuneane. In: J. Am. Chem. Soc., 92, 1970, S. 6366–6368, doi:10.1021/ja00724a061.
  • L. Cessar, P. E. Eaton, J. Halpern: Catalysis of Symmetry-Restricted Reactions by Transition Metal Compounds. The Valence Isomerization of Cubane. In: J. Am. Chem. Soc., 92, 1970, S. 3515–3518, doi:10.1021/ja00714a075.
  • Dongdong Wang, Xiaohong Lyu, Mengtao Sun, Yongqiang Liang: Spectral Analysis on Cuba-Lumacaftor: Cubane as Benzene Bioisosteres of Lumacaftor. In: ACS Omega. Band 8, Nr. 45, 14. November 2023, S. 43332–43340, doi:10.1021/acsomega.3c07532, PMID 38024720, PMC 10652726 (freier Volltext).

nih.gov (Global: 5th place; German: 7th place)

ncbi.nlm.nih.gov

  • Dongdong Wang, Xiaohong Lyu, Mengtao Sun, Yongqiang Liang: Spectral Analysis on Cuba-Lumacaftor: Cubane as Benzene Bioisosteres of Lumacaftor. In: ACS Omega. Band 8, Nr. 45, 14. November 2023, S. 43332–43340, doi:10.1021/acsomega.3c07532, PMID 38024720, PMC 10652726 (freier Volltext).

thieme.de (Global: 2,800th place; German: 167th place)

roempp.thieme.de

  • Eintrag zu Cuban. In: Römpp Online. Georg Thieme Verlag, abgerufen am 28. Dezember 2014.