Тема: Аналитические возможности коммутационной кулонометрии на примере определения гидрохинона

[1] Nagata T. Design of synthetic molecular units including quinones towards the construction of artificial photosynthesis //Research on Chemical Intermediates. – 2014. – Т. 40. – No. 9. – С. 3183-3198
[2] Walker J. E. The NADH: ubiquinone oxidoreductase (complex I) of respiratory chains //Quarterly reviews of biophysics. – 1992. – Т. 25. – No. 03. – С. 253-324.
[3] Fujimoto N., Kosaka T., Yamada M. Menaquinone as well as ubiquinone as a crucial component in the Escherichia coli respiratory chain //Chemical biology. – InTech, 2012.
[4] Tissot P., Huissoud A. Proton effects in the electrochemical behaviour of 2-ethyl-9, 10-anthraquinone in the medium dimethoxyethane-tetrabutylammonium hydroxide with and without oxygen //Electrochimica acta. – 1996. – Т. 41. – No. 15. – С. 2451-2456.
[5] Tandon V. K., Singh R. V., Yadav D. B. Synthesis and evaluation of novel 1, 4-naphthoquinone derivatives as antiviral, antifungal and anticancer agents //Bioorganic & medicinal chemistry letters. – 2004. – Т. 14. – No. 11. – С. 2901-2904.
[6] Kitagawa R. R. et al. Evaluation of mutagenicity and metabolism-mediated cytotoxicity of the naphthoquinone 5-methoxy-3, 4-dehydroxanthomegnin from Paepalanthus latipes //Revista Brasileira de Farmacognosia. – 2015. – Т. 25. – No. 1. – С. 16-21.
[7] Singh D. N. et al. Antifungal anthraquinones from Saprosma fragrans //Bioorganic & medicinal chemistry letters. – 2006. – Т. 16. – No. 17. – С. 4512-4514.
[8] Meazza G., Dayan F. E., Wedge D. E. Activity of quinones on Colletotrichum species //Journal of agricultural and food chemistry. – 2003. – Т. 51. – No. 13. – С. 3824-3828.
[9] da Silva Júnior E. N. et al. The evaluation of quinonoid compounds against Trypanosoma cruzi: synthesis of imidazolic anthraquinones, nor-β-lapachone derivatives and β-lapachone-based 1, 2, 3-triazoles //Bioorganic & medicinal chemistry. – 2010. – Т. 18. – No. 9. – С. 3224-3230.
[10] Ribeiro K. A. L. et al. Activities of naphthoquinones against Aedes aegypti (Linnaeus, 1762) (Diptera: Culicidae), vector of dengue and Biomphalaria glabrata (Say, 1818), intermediate host of Schistosoma mansoni //Acta tropica. – 2009. – Т. 111. – No. 1. – С. 44-50.
[11] da Silva Júnior E. N. et al. 3-Arylamino and 3-alkoxy-nor-β-lapachone derivatives: synthesis and cytotoxicity against cancer cell lines //Journal of medicinal chemistry. – 2009. – Т. 53. – No. 1. – С. 504-508.
[12] Chen Y., Hu L. Design of anticancer prodrugs for reductive activation //Medicinal research reviews. – 2009. – Т. 29. – No. 1. – С. 29-64.
[13] Mallavadhani U. V. et al. Synthesis and anticancer activity of some novel 5, 6-fused hybrids of juglone based 1, 4-naphthoquinones //European journal of medicinal chemistry. – 2014. – Т. 83. – С. 84-91.
[14] Abdel-Lateff A. et al. New antioxidant hydroquinone derivatives from the algicolous marine fungus Acremonium sp //Journal of natural products. – 2002. – Т. 65. – No. 11. – С. 1605-1611
[15] Andersen F. A. et al. Final amended safety assessment of hydroquinone as used in cosmetics //International journal of toxicology. – 2010. – Т. 29. – No. 6_suppl. – С. 274S-287S
...
Купить