An efficient route to 5-(hetero)aryl-2,4′- and 2,2′-bipyridines through readily available 3-pyridyl-1,2,4-triazines

Tetrahedron Letters

Volumn 46, Issue 11, 2005, Pages 1791-1793

  Kozhevnikov, Valery N ^a   Kozhevnikov, Dmitry N ^a   Shabunina, Olga V ^a   Rusinov, Vladimir L ^a   Chupakhin, Oleg N ^a  

^a URAL FEDERAL UNIVERSITY   (Russian Federation)

Author keywords

1,2,4 Triazines; Bipyridines; Ligands; Polypyridines

Indexed keywords

BIPYRIDINE DERIVATIVE; POLYCYCLIC AROMATIC HYDROCARBON DERIVATIVE; TRIAZINE DERIVATIVE;

ARTICLE; CROSS COUPLING REACTION; DIELS ALDER REACTION; NITROSATION; POLYMERIZATION; SYNTHESIS;

BETULACEAE;

EID: 13944258152     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2005.01.135     Document Type: Article

References (19)

1. A. von Zelewsky Stereochemistry of Coordination Compounds 1996 Wiley Chichester
2. E.C. Constable J.-M. Lehn Comprehensive Supramolecular Chemistry Vol. 9 1996 Pergamon 213 252
3. G. Chelucci, and R.P. Thummel Chem. Rev. 102 2002 3129 3170
4. R. Ziessel K. Kalyanasundaram M. Grätzel Photosensitization and Photocatalysis Using Inorganic and Organic Compounds 1993 Kluwer Academic Dordrecht 217 246
5. M.H. Keefe, K.D. Benkstein, and J.T. Hupp Coord. Chem. Rev. 205 2000 201 228
6. A.K. Saha, K. Kross, E.D. Kloszewski, D.A. Upson, J.L. Toner, R.A. Snow, C.D. Black, and V.C. Decai J. Am. Chem. Soc. 115 1993 11032 11033
7. J.C. Loren, and J.S. Siegel Angew. Chem., Int. Ed. 40 2001 754 757
8. B.M. Kelly-Basetti, D.J. Cundy, S.M. Pereira, W.H.F. Sasse, G.P. Savage, and G.W. Simpson Bioorg. Med. Chem. Lett. 5 1995 2989 2992
9. A.C. Thompson Coord. Chem. Rev. 160 1997 1 52
10. G.R. Pabst, O.C. Pfüller, and J. Sauer Tetrahedron 55 1999 8045 8064
11. P.L. Croot, and K.A. Hunter Anal. Chim. Acta 406 2000 289 295
12. Z. Kolarik, U. Mullich, and F. Gassner Solvent Extr. Ion Exch. 17 1999 23 32
13. D.N. Kozhevnikov, V.L. Rusinov, and O.N. Chupakhin A.R. Katritzky Adv. Heterocycl. Chem. Vol. 82 2002 Academic 261 305
14. H. Neunhoeffer A.R. Katrizky C.W. Rees E.F.V. Scriven Comp. Heterocycl. Chem. II Vol. 6 1996 Pergamon Oxford 50 574
15. 5 (235.25) calcd C, 66.37; H, 3.86; N, 29.77. Found C, 66.40; H, 3.91; N, 29.69
16. 3 (233.28) calcd C, 77.23; H, 4.75; N, 18.01. Found C, 77.25; H, 4.72; N, 17.96
17. A. Rykowski, D. Branowska, and J. Kielak Tetrahedron Lett. 41 2000 3657 3658
18. V.N. Kozhevnikov, D.N. Kozhevnikov, T.V. Nikitina, V.L. Rusinov, O.N. Chupakhin, M. Zabel, and B. Koenig J. Org. Chem. 68 2003 2882 2888
19. 3 (273.34) calcd C, 79.10; H, 5.53; N. 15.37. Found C, 79.15; H, 5.42; N, 15.36