Sign In

Login

Password

Forgot Password ? Sign Up

Cuban (German Wikipedia)

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

refsWebsite
Global rank German rank
19doi.org
2nd place
3rd place
1nih.gov
4th place
7th place

doi.org

  • 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

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).