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BODIPY (Japanese Wikipedia)

Analysis of information sources in references of the Wikipedia article "BODIPY" in Japanese language version.

Last modified:

Ref.Un. Ref.Website
Global rank Japanese rank
44doi.org
2nd place
3rd place
11invitrogen.com
low place
low place
11nih.gov
5th place
11th place

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

  • A. Schmitt, B. Hinkeldey, M. Wild, G. Jung (2009). “Synthesis of the Core Compound of the BODIPY Dye Class: 4,4′-Difluoro-4-bora-(3a,4a)-diaza-s-indacene”. J. Fluoresc. 19: 755–759. doi:10.1007/s10895-008-0446-7.
  • K. Tram, H. Yan, H. A. Jenkins, S. Vassiliev, D. Bruce, (2009). “The synthesis and crystal structure of unsubstituted 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY)”. Dyes Pigm 82: 392–395. doi:10.1016/j.dyepig.2009.03.001.
  • I. J. Arroyo, R. Hu, G. Merino, B. Z. Tang, E. Peña-Cabrera (2009). “The Smallest and One of the Brightest. Efficient Preparation and Optical Description of the Parent Borondipyrromethene System”. J. Org. Chem. 74: 5719. doi:10.1021/jo901014w.
  • Loudet, A.; Burgess, K. (2007). “BODIPY Dyes and Their Derivatives: Syntheses and Spectroscopic Properties”. Chem. Rev. 107 (11): 4891–4932. doi:10.1021/cr078381n. PMID 17924696.

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

probes.invitrogen.com

nih.gov (Global: 5th place; Japanese: 11th place)

pubmed.ncbi.nlm.nih.gov

  • Loudet, A.; Burgess, K. (2007). “BODIPY Dyes and Their Derivatives: Syntheses and Spectroscopic Properties”. Chem. Rev. 107 (11): 4891–4932. doi:10.1021/cr078381n. PMID 17924696.