Table of Contents
International Journal of Carbohydrate Chemistry
Volume 2015 (2015), Article ID 235763, 7 pages
http://dx.doi.org/10.1155/2015/235763
Research Article

A New Generation of Glycoconjugated Azo Dyes Based on Aminosugars

1Department of Pharmacy, University of Pisa, Via Bonanno 33, 56126 Pisa, Italy
2School of Chemistry and Chemical Biology, University College Dublin, Belfield, Dublin 4, Ireland

Received 7 May 2015; Revised 13 July 2015; Accepted 14 July 2015

Academic Editor: Vladimir Kren

Copyright © 2015 Lorenzo Guazzelli et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Linked References

  1. H.-K. Rouette, Encyclopedia of Textile Finishing, Springer, Berlin, Germany, 2001. View at Publisher · View at Google Scholar
  2. J. H. Hofenk de Graaf, The Colourful Past. Origins, Chemistry and Identification of Natural Dyestuffs, Abegg-Stitung, Riggsberg, Switzerland; Archetype Pubblications, London, UK, 2004.
  3. M. Neamtu, I. Siminiceanu, A. Yediler, and A. Kettrup, “Kinetics of decolorization and mineralization of reactive azo dyes in aqueous solution by the UV/H2O2 oxidation,” Dyes and Pigments, vol. 53, no. 2, pp. 93–99, 2002. View at Publisher · View at Google Scholar · View at Scopus
  4. G. Bartalucci, R. Bianchini, G. Catelani, F. D'Andrea, and L. Guazzelli, “Naturalised dyes: a simple straightforward synthetic route to a new class of dyes—glycoazodyes (GADs),” European Journal of Organic Chemistry, no. 4, pp. 588–595, 2007. View at Publisher · View at Google Scholar · View at Scopus
  5. R. Bianchini, G. Catelani, R. Cecconi et al., “‘Naturalization’ of textile disperse dyes through glycoconjugation: the case of a bis(2-hydroxyethyl) group containing azo dye,” Carbohydrate Research, vol. 343, no. 12, pp. 2067–2074, 2008. View at Publisher · View at Google Scholar · View at Scopus
  6. R. Bianchini, G. Catelani, R. Cecconi et al., “Ethereal glycoconjugated azodyes (GADs): a new group of water-soluble, naturalised dyes,” European Journal of Organic Chemistry, no. 3, pp. 444–454, 2008. View at Publisher · View at Google Scholar · View at Scopus
  7. A. Porri, R. Baroncelli, L. Guglielminetti et al., “Fusarium oxysporum degradation and detoxification of a new textile-glycoconjugate azo dye (GAD),” Fungal Biology, vol. 115, no. 1, pp. 30–37, 2011. View at Publisher · View at Google Scholar · View at Scopus
  8. J. Isaad, M. Rolla, and R. Bianchini, “Synthesis of water-soluble large naturalised dyes through double glycoconjugation,” European Journal of Organic Chemistry, no. 17, pp. 2748–2764, 2009. View at Publisher · View at Google Scholar · View at Scopus
  9. R. Bianchini, M. Rolla, J. Isaad et al., “Efficient double glycoconjugation to naturalize high molecular weight disperse dyes,” Carbohydrate Research, vol. 356, pp. 104–109, 2012. View at Publisher · View at Google Scholar · View at Scopus
  10. D. D. Perrin, W. L. F. D. Armarego, and R. Perrin, Purification of Laboratory Chemicals, Pergamon Press, Oxford, UK, 2nd edition, 1980.
  11. J. Yang, X. Fu, Q. Jia et al., “Studies on the substrate specificity of Escherichia coli galactokinase,” Organic Letters, vol. 5, no. 13, pp. 2223–2226, 2003. View at Publisher · View at Google Scholar · View at Scopus
  12. H. Wahl, Y. Arnould, and M. Simon, “Dyes for cellulose acetate. II. Poly(hydroxyethyl)aniline dyes,” Bulletin de la Societe Chimique de France, pp. 366–369, 1952. View at Google Scholar
  13. M. Kunishima, C. Kawachi, F. Iwasaki, K. Terao, and S. Tani, “Synthesis and characterization of 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)- 4-methylmorpholinium chloride,” Tetrahedron Letters, vol. 40, no. 29, pp. 5327–5330, 1999. View at Publisher · View at Google Scholar · View at Scopus
  14. J. Sharma, D. Batovska, Y. Kuwamori, and Y. Asano, “Enzymatic chemoselective synthesis of secondary-amide surfactant from N-methylethanol amine,” Journal of Bioscience and Bioengineering, vol. 100, no. 6, pp. 662–666, 2005. View at Publisher · View at Google Scholar · View at Scopus