Synthesis and structure elucidation of oxidative coupling products of 2-hydroxy-1,4-naphthoquinones

Russian Chemical Bulletin

Volumn 55, Issue 2, 2006, Pages 301-305

  Yakubovskaya, A Ya ^a   Kochergina, T Yu ^a   Denisenko, V A ^a   Berdyshev, D V ^a   Glazunov, V P ^a   Anufriev, V Ph ^a  

^a PACIFIC INSTITUTE OF BIOORGANIC CHEMISTRY   (Russian Federation)

Author keywords

2,3 dihydro 3 O (1,4 naphthoquinon 2 yl) 2 oxo 1,4 naphthoquinone; 2,5(8) dihydroxy 1,4 naphthoquinone; 2,5,8 trihydroxy 1,4 naphthoquinone; 2 hydroxy 1,4 naphthoquinone; Density functional theory; Lead dioxide; Oxidative coupling

Indexed keywords

EID: 33747070827     PISSN: 10665285     EISSN: None     Source Type: Journal    
DOI: 10.1007/s11172-006-0252-9     Document Type: Article

References (20)

1. L. S. Stepanenko, O. E. Krivoshchekova, P. S. Dmitrenok, and O. B. Maximov, Phytochemistry, 1997, 46, 565.
2. A. Ya. Chizhova, T. Yu. Kochergina, V. Ph. Anufriev, V. A. Denisenko, and V. P. Glazunov, Izv. Akad. Nauk, Ser. Khim., 1999, 947
3. [Russ. Chem. Bull., 1999, 48, 938 (Engl. Transl.)].
4. S. C. Hooker, J. Am. Chem. Soc., 1936, 58, 1168.
5. M. J. Ettlinger, J. Am. Chem. Soc., 1950, 72, 3472.
6. L. J. Bellamy, The Infra-red Spectra of Complex Molecules, Chapman and Hall, London, 1975, 133.
7. A. Ya. Tchizhova, V. Ph. Anufriev, V. P. Glazunov, and V. A. Denisenko, Izv. Akad. Nauk, Ser. Khim., 2000, 465
8. [Russ. Chem. Bull., Int. Ed., 2000, 49, 466].
9. A. Ya. Tchizhova, V. Ph. Anufriev, V. P. Glazunov, V. A. Denisenko, and O. P. Moiseenko, Synth. Commun., 1999, 29, 3971.
10. A. Ya. Tchizhova, Ph. D. (Chem.) Thesis, Pacific Institute of Bioorganic Chemistry, Far-Eastern Branch of the Russian Academy of Sciences, Vladivostok, 1996, 155 pp. (in Russian).
11. G. V. Malinovskaya, A. Ya. Chizhova, and V. Ph. Anufriev, Izv. Akad. Nauk, Ser. Khim., 1999, 1019
12. [Russ. Chem. Bull., 1999, 48, 1010 (Engl. Transl.)].
13. N. Donaldson, The Chemistry and Technology of Naphthalene Compounds, Arnold, London, 1960.
14. H. Singh, T. L. Folk, and P. J. Scheuer, Tetrahedron, 1969, 25, 5301.
15. J. P. Perdew, K. Burke, and M. Ernzerhof, Phys. Rev. Lett., 1996, 787, 3865.
16. D. N. Laikov, Chem. Phys. Lett., 1997, 281, 151.
17. M. W. Schmidt, K. K. Baldridge, J. A. Boatz, S. T. Elbert, M. S. Gordon, J. H. Jensen, S. Koseki, N. Matsunaga, K. A. Nguyene, S. J. Su, T. L. Widus, M. Dupuis, and J. A. Montgomery, J. Comput. Chem., 1993, 14, 1347.
18. P. J. Stevens, F. J. Devlin, C. F. Chablowski, and M. J. Frish, J. Phys. Chem., 1994, 98, 11623.
19. C. F. Koelsch and D. J. Byers, J. Am. Chem. Soc., 1940, 62, 560.
20. L. F. Fieser and M. Fieser, Reagents for Organic Synthesis, J. Wiley and Sons, New York-London-Sydney, 1968.