Technologies of Halogenation of Hydroxyanthraquinones
Commenced in January 2007
Frequency: Monthly
Edition: International
Paper Count: 32795
Technologies of Halogenation of Hydroxyanthraquinones

Authors: Dmitriy Yu. Korulkin, Raissa A. Muzychkina

Abstract:

In review the generalized data about different methods of synthesis of biological activity halogenated di-, tri- and tetrahydroxyanthraquinones is presented. The basic regularity of a synthesis is analyzed. Action of temperature, pH, solubility, catalysts and other factors on a reaction product yield is revealed.

Keywords: Electrophilic substitution, halogenation, hydroxyanthraquinones, physiologically active substances.

Digital Object Identifier (DOI): doi.org/10.5281/zenodo.1099916

Procedia APA BibTeX Chicago EndNote Harvard JSON MLA RIS XML ISO 690 PDF Downloads 2143

References:


[1] V. Susumu, M. Takido, J. Pharm. Soc. Japan, vol. 106, no. 4, pp. 302- 306, 1986.
[2] L. B. Demirezer, I. Bergere, H.-J. Schiewe, Pharmazie, vol. 49, no. 5, pp. 378-379, 1994.
[3] S. C. Montoya, A. M. Agnese, Phytomedicine, vol. 10, pp. 569-574, 2003.
[4] R. A. Muzychkina, D. Yu. Korulkin, The modified anthraquinones, Almaty: CBB Globus, 2013.
[5] R. A. Muzychkina, Natural Anthraquinones. Biological Properties and Physicochemical Characteristics, Moscow: Phasis, 1998.
[6] J. V. Bergman, J. Amer. Chem. Soc., vol. 113, no. 18, pp. 6982-6998, 1991.
[7] P. Sutter, C. D. Weis, Dyes and Pigments, vol. 6, no. 6, pp. 435-443, 1985.
[8] C. H. Chen, C.-Y. Shaw, C.-C. Chen, Y.-C. H.Tsai, J. Nat. Prod., vol. 65, pp. 740-741, 2002.
[9] C.-Y. Chen, Y. Lu, Z.-N. Chen, Acta Univ. Med. Second. Shanghai, vol. 21, pp. 488-491, 2001.
[10] Z.-T. Zhang, Y.-J. Du, Q.-G. Liu, Y. Liu, Nat. Prod. Res. Dev., vol. 13, pp. 45-47, 2001.
[11] Wu. Tuang-Shung, T.-T. Jond, H. J. Then, Phytochem., vol. 26, no. 6, pp. 1623-1625, 1987.
[12] H. Jayasuriya, N. M. Koonchanok, J. L. Mclaughlin, J. Natur. Prod., vol. 55, no. 5, pp. 696-698, 1992.
[13] J. Messawa, F. Ferrari, Phytochem., vol. 30, no. 2, pp. 708-710, 1991.
[14] L. Frances, Phytochem., vol. 35, no. 3, pp. 685-686, 1994.
[15] B. Botta, G. Cassinelli, C. Geroni, F. Delle Monache, Phytochem., vol. 22, no. 2, pp. 539-542, 1983.
[16] K. Katsuura, Y. Hanasaki, V. Sniescus, Tetrahedron Lett., no. 1, pp. 9- 12, 1985.
[17] K. Nakamura, T. Assai, T. Hara, Bull. Chem. Soc. Japan, vol. 56, no. 5, pp. 1435-1439, 1983.
[18] H. Itokawa, M. Kazuhiko, T. Koichi, Y. Oiac, Phytochem., vol. 28 no. 12, pp. 3465-3468, 1989.
[19] J. L. Bloomer, K. W. Stagliano, B.-G. Wang, J. Org. Chem., vol. 58 no. 27, pp. 7906-7912, 1993.