バナジルアセチルアセトナート (Japanese Wikipedia)

Analysis of information sources in references of the Wikipedia article "バナジルアセチルアセトナート" in Japanese language version.

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doi.org

  • Richard A. Rowe, Mark M. Jones (1957). “Vanadium(IV) Oxy(acetylacetonate)”. Inorg. Synth.. Inorganic Syntheses 5: 113–116. doi:10.1002/9780470132364.ch30. ISBN 978-0-470-13236-4. 
  • Takashi Itoh, Koichiro Jitsukawa, Kiyotomi Kaneda, Shiichiro Teranishi (1979). “Vanadium-catalyzed epoxidation of cyclic allylic alcohols. Stereoselectivity and stereocontrol mechanism”. J. Am. Chem. Soc. 101 (1): 159–169. doi:10.1021/ja00495a027. 
  • Bryant E. Rossiter, Hsyueh-Liang Wu, Toshikazu Hirao "Vanadyl Bis(acetylacetonate)" in Encyclopedia of Reagents for Organic Synthesis John Wiley & Sons, 2007. doi:10.1002/047084289X.rv003m.pub2. Article Online Posting Date: March 15, 2007
  • Mohamad Z. Mehdi and Ashok K. Srivastava (2005). “Organo-vanadium compounds are potent activators of the protein kinase B signaling pathway and protein tyrosine phosphorylation: Mechanism of insulinomimesis”. ABB 440 (2): 158–164. doi:10.1016/j.abb.2005.06.008. PMID 16055077. 

nih.gov

pubmed.ncbi.nlm.nih.gov

  • Mohamad Z. Mehdi and Ashok K. Srivastava (2005). “Organo-vanadium compounds are potent activators of the protein kinase B signaling pathway and protein tyrosine phosphorylation: Mechanism of insulinomimesis”. ABB 440 (2): 158–164. doi:10.1016/j.abb.2005.06.008. PMID 16055077. 

wikipedia.org

en.wikipedia.org

  • Richard A. Rowe, Mark M. Jones (1957). “Vanadium(IV) Oxy(acetylacetonate)”. Inorg. Synth.. Inorganic Syntheses 5: 113–116. doi:10.1002/9780470132364.ch30. ISBN 978-0-470-13236-4. 
  • Mohamad Z. Mehdi and Ashok K. Srivastava (2005). “Organo-vanadium compounds are potent activators of the protein kinase B signaling pathway and protein tyrosine phosphorylation: Mechanism of insulinomimesis”. ABB 440 (2): 158–164. doi:10.1016/j.abb.2005.06.008. PMID 16055077.