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ヘキサフルオロリン酸1-ブチル-3-メチルイミダゾリウム (Japanese Wikipedia)

Analysis of information sources in references of the Wikipedia article "ヘキサフルオロリン酸1-ブチル-3-メチルイミダゾリウム" in Japanese language version.

refsWebsite
Global rank Japanese rank
6doi.org
2nd place
6th place
2nih.gov
4th place
24th place
1carlroth.com
low place
low place
1books.google.com
3rd place
61st place
1orgsyn.org
2,971st place
1,173rd place
1nb.rs
3,800th place
low place

books.google.com (Global: 3rd place; Japanese: 61st place)

  • Mihkel Koel (2008). Ionic Liquids in Chemical Analysis. CRC Press. p. xxvii. ISBN 978-1-4200-4646-5. https://books.google.com/books?id=y8d9F7NG60cC&pg=PR27 

carlroth.com (Global: low place; Japanese: low place)

doi.org (Global: 2nd place; Japanese: 6th place)

  • R.P. Swatloski; J.D. Holbrey & R.D. Rogers (2003). “Ionic liquids are not always green: hydrolysis of 1-butyl-3-methylimidazolium hexafluorophosphate”. Green Chem. 5 (4): 361–363. doi:10.1039/b304400a. 
  • Poliane K. Batista, João Marcos G. de O. Ferreira, Fabio P. L. Silva, Mario L. A. A Vasconcellos, Juliana A. Vale (31 May 2019), “The Role Ionic Liquid [BMIM][PF6] in One-Pot Synthesis of Tetrahydropyran Rings through Tandem Barbier–Prins Reaction”, Molecules, vol. 24, no. 11, p. 2084, doi:10.3390/molecules24112084, PMC 6600659, PMID 31159274{{citation2}}: CS1メンテナンス: 明示されていないフリーアクセスDOI (カテゴリ) CS1メンテナンス: 複数の名前/author (カテゴリ)
  • Jhillu S. Yadav, Basi V. S. Reddy, Kamakolanu Uma Gayathri, Attaluri R. Prasad (2003), “[Bmim]PF6/RuCl3·xH2O: a novel and recyclable catalytic system for the oxidative coupling of β-naphthols”, New J. Chem., vol. 27, no. 12, pp. 1684–1686, doi:10.1039/B307253N{{citation2}}: CS1メンテナンス: 複数の名前/author (カテゴリ)
  • Gurpreet Kaur, Aditi Sharma, Bubun Banerjee (2018), “[Bmim]PF6: An efficient tool for the synthesis of diverse bioactive heterocycles”, Journal of the Serbian Chemical Society, vol. 83, no. 10, pp. 1071–1097, doi:10.2298/JSC180103052K, 2021年2月12日閲覧{{citation2}}: CS1メンテナンス: 複数の名前/author (カテゴリ)
  • Álvaro Pérez-Salado Kamps, Dirk Tuma, Jianzhong Xia, Gerd Maurer (2003), Solubility of CO2 in the Ionic Liquid [bmim] [PF6], 48, pp. 746–749, doi:10.1021/je034023f 
  • Yeonji Oh, Xile Hu (2015), Ionic liquids enhance the electrochemical CO2 reduction catalyzed by MoO2, 51, pp. 13698–13701, doi:10.1039/C5CC05263G 

nb.rs (Global: 3,800th place; Japanese: low place)

doiserbia.nb.rs

nih.gov (Global: 4th place; Japanese: 24th place)

ncbi.nlm.nih.gov

  • Poliane K. Batista, João Marcos G. de O. Ferreira, Fabio P. L. Silva, Mario L. A. A Vasconcellos, Juliana A. Vale (31 May 2019), “The Role Ionic Liquid [BMIM][PF6] in One-Pot Synthesis of Tetrahydropyran Rings through Tandem Barbier–Prins Reaction”, Molecules, vol. 24, no. 11, p. 2084, doi:10.3390/molecules24112084, PMC 6600659, PMID 31159274{{citation2}}: CS1メンテナンス: 明示されていないフリーアクセスDOI (カテゴリ) CS1メンテナンス: 複数の名前/author (カテゴリ)

pubmed.ncbi.nlm.nih.gov

  • Poliane K. Batista, João Marcos G. de O. Ferreira, Fabio P. L. Silva, Mario L. A. A Vasconcellos, Juliana A. Vale (31 May 2019), “The Role Ionic Liquid [BMIM][PF6] in One-Pot Synthesis of Tetrahydropyran Rings through Tandem Barbier–Prins Reaction”, Molecules, vol. 24, no. 11, p. 2084, doi:10.3390/molecules24112084, PMC 6600659, PMID 31159274{{citation2}}: CS1メンテナンス: 明示されていないフリーアクセスDOI (カテゴリ) CS1メンテナンス: 複数の名前/author (カテゴリ)

orgsyn.org (Global: 2,971st place; Japanese: 1,173rd place)