Site directed nuclear bromination of aromatic compounds by an electrochemical method

Tetrahedron Letters

Volumn 47, Issue 27, 2006, Pages 4581-4584

  Raju, T ^a   Kulangiappar, K ^a   Anbu Kulandainathan, M ^a   Uma, U ^a   Malini, R ^a   Muthukumaran, A ^a  

^a CENTRAL ELECTROCHEMICAL RESEARCH INSTITUTE   (India)

Author keywords

Electrochemical bromination; Regioselectivity; Site directed bromination; Two phase electrolysis

Indexed keywords

AROMATIC COMPOUND; HYDROXYL GROUP;

ARTICLE; BROMINATION; ELECTROCHEMICAL ANALYSIS; ELECTROLYSIS; ELECTRON;

EID: 33744545231     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2006.04.152     Document Type: Article

References (27)

1. Ullman's Encyclopedia of Industrial Chemistry, 6th ed.; Wiley-VCH: Weinheim, 1998, Electronic release.
2. Roy S.C., Guin C., Rana K.K., and Maiti G. Tetrahedron Lett. 42 (2001) 6941
3. Butler A., and Walker J.V. Chem. Rev. 93 (1993) 1937
4. Chaudhuri M.K., Khan A.T., and Patel B.K. Tetrahedron Lett. 39 (1998) 8163
5. Buckles R.E., Popov A.I., Zelezny W.F., and Smith R.J. J. Am. Chem. Soc. 73 (1951) 4525
6. Muathen H.A. J. Org. Chem. 57 (1992) 2740
7. Fieser L.F., and Fieser M. Reagents for Organic Synthesis (1967), Wiley, New York p 967
8. Casalbore G., Mastragostino M., and Valcher S. J. Electroanal. Chem. 87 (1978) 411
9. Casalbore G., Mastragostino M., and Valcher S. J. Electroanal. Chem. 77 (1977) 373
10. Casalbore G., Mastragostino M., and Valcher S. J. Electroanal. Chem. 61 (1975) 33
11. Lerman O., and Rozen S. J. Flourine Chem. 45 (1989) 104
12. Chaudberg B.M., Sudha Y., and Reddy P.N. Synlett (1994) 450
13. Rose D.J. J. Chem. Res. (S) (1997) 432
14. Clague M.H., and Butler A. J. Am. Chem. Soc. 117 (1995) 3475
15. Roche D., Prasad K., Repic O., and Blacklok T.J. Tetrahedron Lett. 41 (2000) 2083
16. Smith K., El-Hiti G.A., Hammond M.E.W., Bahzad D., Li Z., and Siquet C. J. Chem. Soc., Perkin Trans. 1 (2000) 2745
17. Kim E.H., Koo B.S., Song C.E., and Lee K. J. Synth. Commun. 31 (2001) 3627
18. Lee K.J., Cho H.K., and Song C.E. Bull. Korean Chem. Soc. 23 (2002) 773
19. Firouzabadi H., Iranpoor N., and Amani K. J. Mol. Cat. A: Chem. (2002) 3853
20. Park M.Y., Yang S.G., Jadhav V., and Kim Y.H. Tetrahedron Lett. 45 (2004) 4887
21. Vahei R.G., and Jalili H. Synthesis (2005) 1103
22. Tuyen V.N., Kesteleyn B., and De Kimpe N. Tetrahedron 58 (2002) 121
23. Carmen C.M., Ruano Jose.G., Gema S., Miguel A., and Antorio U. Synlett (1997) 1241
24. Yadav J.S., Reddy B.V.S., Reddy P.S.R., Basak A.K., and Narsaish A.V. Adv. Synth. Catal. 346 (2004) 77
25. Ganguly N.C., De P., and Dutta S. Synthesis (2005) 1099
26. Raju T., Kulangiappar K., Anbukulandainathan M., and Muthukumaran A. Tetrahedron Lett. 46 (2005) 7047
27. 3): δ = 7.91 (d, 1H, J = 8.1 Hz), 7.72-7.74 (m, 2H), 7.56 (t, 1H, J = 8.2 Hz), 7.41 (t, 1H, J = 8.2 Hz), 7.28 (d, 1H, J = 8.1 Hz).