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Acetonitril (German Wikipedia)

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

refsWebsite
Global rank German rank
14doi.org
2nd place
3rd place
2europa.eu
68th place
29th place
2google.de
2,106th place
139th place
2dguv.de
813th place
69th place
1reach-clp-biozid-helpdesk.de
low place
979th place
1suva.ch
low place
1,619th place
1merckmillipore.com
9,664th place
717th place
1harvard.edu
18th place
181st place
1heise.de
766th place
46th place
1ed.ac.uk
1,871st place
4,217th place
1inrs.fr
low place
low place
1inchem.org
4,334th place
5,795th place
1epa.gov
882nd place
2,545th place

dguv.de

gestis.dguv.de

dguv.de

doi.org

  • Frederick G. Bordwell: Equilibrium Acidities in Dimethyl Sulfoxide Solution. In: Accounts of Chemical Research. Band 21, 1988, S. 456–463, doi:10.1021/ar00156a004.
  • P. Alston Steiner, W. Gordy: Precision measurement of dipole moments and other spectral constants of normal and deuterated methyl fluoride and methyl cyanide. In: Journal of Molecular Spectroscopy. Band 21, Nr. 1-4, Januar 1966, S. 291–301, doi:10.1016/0022-2852(66)90152-4.
  • Ziguo Yuan, Xin Zhang, Qian Yao, Ying Zhang, Yao Fu: Production of acetonitrile via catalytic fast pyrolysis of biomass derived polylactic acid under ammonia atmosphere. In: Journal of Analytical and Applied Pyrolysis. Band 140, Juni 2019, S. 376–384, doi:10.1016/j.jaap.2019.04.017.
  • Elizabeth Rojas, Juan J. Delgado, M. Olga Guerrero-Pérez, Miguel A. Bañares: Performance of NiO and Ni–Nb–O active phases during the ethane ammoxidation into acetonitrile. In: Catalysis Science & Technology. Band 3, Nr. 12, 2013, S. 3173, doi:10.1039/c3cy00415e.
  • Takashi Tatsumi, Shigeki Kunitomi, Jun Yoshiwara, Atsushi Muramatsu, Hiro-o Tominaga: Synthesis of acetonitrile and related compounds from CO-H2-NH3 over Mo/SiO2. In: Catalysis Letters. Band 3, Nr. 3, 1989, S. 223–226, doi:10.1007/BF00766397.
  • K Kim: The selective synthesis of acetonitrile from carbon monoxide, hydrogen, and ammonia over MO/SiO2. In: Journal of Catalysis. Band 137, Nr. 1, September 1992, S. 127–138, doi:10.1016/0021-9517(92)90144-7.
  • Emily C. Corker, Uffe V. Mentzel, Jerrik Mielby, Anders Riisager, Rasmus Fehrmann: An alternative pathway for production of acetonitrile: ruthenium catalysed aerobic dehydrogenation of ethylamine. In: Green Chemistry. Band 15, Nr. 4, 2013, S. 928, doi:10.1039/c3gc36513a.
  • Elizabeth Rojas, M. Olga Guerrero-Pérez, Miguel A. Bañares: Niobia-Supported Nanoscaled Bulk-NiO Catalysts for the Ammoxidation of Ethane into Acetonitrile. In: Catalysis Letters. Band 143, Nr. 1, Januar 2013, S. 31–42, doi:10.1007/s10562-012-0937-7.
  • Fernando Rubio‐Marcos, Elizabeth Rojas, Ricardo López‐Medina, M. Olga Guerrero‐Pérez, Miguel A. Bañares, José F. Fernandez: Tuning of Active Sites in NiNbO Catalysts for the Direct Conversion of Ethane to Acetonitrile or Ethylene. In: ChemCatChem. Band 3, Nr. 10, 17. Oktober 2011, S. 1637–1645, doi:10.1002/cctc.201100115.
  • Conor Hamill, Hafedh Driss, Alex Goguet, Robbie Burch, Lachezar Petrov, Muhammad Daous, David Rooney: Mild temperature palladium-catalyzed ammoxidation of ethanol to acetonitrile. In: Applied Catalysis A: General. Band 506, Oktober 2015, S. 261–267, doi:10.1016/j.apcata.2015.09.030.
  • Lawrence J. Winters, Ernest Grunwald: Organic Reactions Occurring in or on Micelles. III. Reaction of Methyl Bromide with Cyanide Ion 1,2. In: Journal of the American Chemical Society. Band 87, Nr. 20, Oktober 1965, S. 4608–4611, doi:10.1021/ja00948a037.
  • Robert West, Gerald A. Gornowicz: Polylithium compounds. IV. Polylithiation of nitriles and the preparations of trisilyl ynamines. In: Journal of the American Chemical Society. Band 93, Nr. 7, April 1971, S. 1714–1720, doi:10.1021/ja00736a025.
  • P. M. Osterberg, J. K. Niemeier, C. J. Welch, J. M. Hawkins, J. R. Martinelli, T. E. Johnson, T. W. Root, S. S. Stahl: Experimental Limiting Oxygen Concentrations for Nine Organic Solvents at Temperatures and Pressures Relevant to Aerobic Oxidations in the Pharmaceutical Industry. In: Org. Process Res. Dev. 19, 2015, S. 1537–1542, doi:10.1021/op500328f
  • William G. Killian, Andrew T. Norfleet, Carl T. Lira: Densities of Selected Deuterated Solvents. In: Journal of Chemical & Engineering Data. Band 67, Nr. 4, 14. April 2022, S. 893–901, doi:10.1021/acs.jced.1c00990.

ed.ac.uk

homepages.ed.ac.uk

  • Jack Ponton: Azeotrope Databank. (Queriable database) The Edinburgh Collection of Open Software for Simulation and Education, Edinburgh University, September 2001, abgerufen am 20. Februar 2008.

epa.gov

europa.eu

echa.europa.eu

google.de

  • Harold A. Wittcoff, Bryan G. Reuben, Jeffery S. Plotkin: Industrial Organic Chemicals. John Wiley & Sons, 2004, ISBN 978-0-471-44385-8, S. 181–183 (google.de [abgerufen am 31. Juli 2024]).
  • Erlenmeyer: Erlenmeyer's Lehrbuch der organischen Chemie. C. F. Winter'sche Verlagshandlung, 1883, S. 352–353 (google.de [abgerufen am 31. Juli 2024]).

harvard.edu

ui.adsabs.harvard.edu

  • B. L. Ulrich, E. K. Conklin: Detection of Methyl Cyanide in Comet Kohoutek (1973f). In: Bulletin of the American Astronomical Society. Vol. 6, 1974, S. 389 (bibcode:1974BAAS....6..389S).

heise.de

inchem.org

  • Environmental Health Criteria (EHC) für Acetonitrile, abgerufen am 29. November 2014.

inrs.fr

merckmillipore.com

reach-clp-biozid-helpdesk.de

suva.ch