Display options
Cite
Weiss H, Reichel J, Görls H, et al. Curcuminoid-BF. Beilstein J Org Chem. 2017;13:2264-2272doi: 10.3762/bjoc.13.223.
Weiss, H., Reichel, J., Görls, H., Schneider, K. R. A., Micheel, M., Pröhl, M., Gottschaldt, M., Dietzek, B., & Weigand, W. (2017). Curcuminoid-BF. Beilstein journal of organic chemistry, 132264-2272. https://doi.org/10.3762/bjoc.13.223
Weiss, Henning, et al. "Curcuminoid-BF." Beilstein journal of organic chemistry vol. 13 (2017): 2264-2272. doi: https://doi.org/10.3762/bjoc.13.223
Weiss H, Reichel J, Görls H, Schneider KRA, Micheel M, Pröhl M, Gottschaldt M, Dietzek B, Weigand W. Curcuminoid-BF. Beilstein J Org Chem. 2017 Oct 26;13:2264-2272. doi: 10.3762/bjoc.13.223. eCollection 2017. PMID: 29114330; PMCID: PMC5669223.
Copy Download .nbib Format: NLM
Share it on

Beilstein J Org Chem. 2017 Oct 26;13:2264-2272. doi: 10.3762/bjoc.13.223. eCollection 2017.

Curcuminoid-BF.

Beilstein journal of organic chemistry

Henning Weiss, Jeannine Reichel, Helmar Görls, Kilian Rolf Anton Schneider, Mathias Micheel, Michael Pröhl, Michael Gottschaldt, Benjamin Dietzek, Wolfgang Weigand

Affiliations

  1. Institute for Inorganic and Analytical Chemistry, Friedrich-Schiller-Universität Jena, Humboldtstrasse 8, 07743 Jena, Germany.
  2. Institute for Physical Chemistry, Friedrich-Schiller-Universität Jena, Helmholtzweg 4, 07743 Jena, Germany.
  3. Leibniz Institute of Photonic Technology (IPHT), Albert-Einstein-Straße 9, 07745 Jena, Germany.
  4. Jena Center of Soft Matter, Friedrich-Schiller-Universität Jena, Philosophenweg 7, 07743 Jena, Germany.

PMID: 29114330 PMCID: PMC5669223 DOI: 10.3762/bjoc.13.223

Abstract

Eight difluoroboron complexes of curcumin derivatives carrying alkyne groups containing substituents have been synthesized following an optimised reaction pathway. The complexes were received in yields up to 98% and high purities. Their properties as fluorescent dyes have been investigated. Furthermore, a strategy for the hydrolysis of the BF

Keywords: BF2 complex; curcumin; dyes; fluorescence; hydrolysis; spectroscopy

References

  1. Metallomics. 2011 Oct;3(10):987-90 - PubMed
  2. J Med Chem. 1998 Oct 8;41(21):3948-60 - PubMed
  3. Arzneimittelforschung. 2002;52(2):120-4 - PubMed
  4. Tetrahedron Lett. 2013 Apr 17;54(16):2070-2073 - PubMed
  5. Angew Chem Int Ed Engl. 2012 May 29;51(22):5308-32 - PubMed
  6. Eur J Med Chem. 2016 May 4;113:34-49 - PubMed
  7. Dalton Trans. 2014 Feb 28;43(8):3072-86 - PubMed
  8. Inorg Chem. 2015 Sep 8;54(17):8560-70 - PubMed
  9. Indian J Pharm Sci. 2011 May;73(3):262-70 - PubMed
  10. Bioorg Med Chem Lett. 2009 Dec 15;19(24):7003-6 - PubMed
  11. Bioorg Chem. 2012 Feb;40(1):30-8 - PubMed
  12. Planta Med. 1991 Feb;57(1):1-7 - PubMed
  13. Dalton Trans. 2016 Nov 29;45(47):18876-18891 - PubMed
  14. Dalton Trans. 2016 Aug 2;45(31):12283-7 - PubMed
  15. Dalton Trans. 2011 Mar 7;40(9):2006-16 - PubMed
  16. Org Biomol Chem. 2014 Mar 14;12(10):1618-26 - PubMed
  17. Nat Rev Immunol. 2008 Nov;8(11):837-48 - PubMed
  18. J Med Chem. 2005 Mar 24;48(6):1941-7 - PubMed
  19. Cancer Lett. 1985 Nov;29(2):197-202 - PubMed
  20. Angew Chem Int Ed Engl. 2002 Jul 15;41(14):2596-9 - PubMed
  21. Spectrochim Acta A Mol Biomol Spectrosc. 2013 Mar 15;105:267-72 - PubMed
  22. Photochem Photobiol. 2000 Nov;72(5):625-31 - PubMed
  23. Org Lett. 2003 Feb 6;5(3):349-52 - PubMed

Publication Types