An efficient copper-catalysed aerobic oxybromination of arenes in water

Green Chemistry

Volumn 12, Issue 12, 2010, Pages 2124-2126

  Wang, Jian ^a   Wang, Wei ^a   Li, Jing Hua ^a  

^a ZHEJIANG UNIVERSITY OF TECHNOLOGY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 78649814386     PISSN: 14639262     EISSN: 14639270     Source Type: Journal    
DOI: 10.1039/c0gc00328j     Document Type: Article

References (45)

1. I. P. Beletskaya A. V. Cheprakov Chem. Rev. 2000 100 3009.
2. F. Diederich and P. J. Stang, Metal-Catalysed Cross-Coupling Reactions, Wiley-VCH, Weinheim, Germany, 1998.
3. S. G. Davis, Organotransition Metal Chemistry: Application to Organic Synthesis, Pergamon Press, Oxford, 1982.
4. Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim, 6th edn, 2002.
5. R. Taylor Electrophilic Aromatic Substitution, Wiley, Chichester, 1990.
6. Kirk-Othmer Encyclopedia of Chemical Technology, Wiley, New York, 6th edn, 1993, vol. 5.
7. M. M. Heravi; N. Abdolhosseini H. A. Oskooie Tetrahedron Lett. 2005 46 8959-8963.
8. H. E. Podall W. E. Foster J. Org. Chem. 1958 23 280.
9. G. M. Kosolapoff J. Am. Chem. Soc. 1953 75 3596.
10. K. Venkateswarlu K. Suneel B. Das K. N. Reddy T. S. Reddy Synth. Commun. 2009 39 215.
11. B. Das K. Venkateswarlu M. Krishnaiah H. Holla Tetrahedron Lett. 2006 47 8693.
12. N. C. Ganguly P. De S. Dutta Synthesis 2005 1103.
13. T. Oberhauser J. Org. Chem. 1997 62 4504.
14. L. Horner E. H. Winkelmann Angew. Chem. 1959 71 349.
15. O. Stark Ber. Dtsch. Chem. Ges. 1910 43 670.
16. S. Adimurthy G. Ramachandraiah A. V. Bedekar S. Ghosh B. C. Ranu P. Ghosh Green Chem. 2006 8 916.
17. D. Kikuchi S. Sakaguchi Y. Ishii J. Org. Chem. 1998 63 6023.
18. D. Kikuchi S. Sakaguchi Y. Ishii J. Org. Chem. 1998 63 6023.
19. B. Fuchs Y. Belsky E. Tartakovsky J. Zizuashvili S. Weinman J. Chem. Soc., Chem. Commun. 1982 778.
20. F. Toda J. Schmeyers Green Chem. 2003 5 701.
21. B. Fuchs Y. Belsky E. Tartakovsky J. Zizuashvili S. Weinman J. Chem. Soc., Chem. Commun. 1982 778.
22. C. Le Z. Chen Y. Hu Chin. J. Chem. 2005 23 1537.
23. J. Salazar R. Dorta Synlett 2004 1318.
24. N. Iranpoor H. Firouzabadi R. Azadi Tetrahedron Lett. 2006 47 5531.
25. S. P. Borikar T. Daniel V. Paul Tetrahedron Lett. 2009 50 1007.
26. V. Kavala S. Naik B. K. Patel J. Org. Chem. 2005 70 4267.
27. N. P. Buu-Hoi P. Demerseman J. Org. Chem. 1953 18 649.
28. H. Adibi A. B. Hajipour M. Hashemi Tetrahedron Lett. 2007 48 1255.
29. G. Majetich R. Hicks S. Reister J. Org. Chem. 1997 62 4321.
30. B. Ganchegui W. Leitner Green Chem. 2007 9 26.
31. C. Limberg J. H. Teles Adv. Synth. Catal. 2001 343 447.
32. J. Dakka Y. Sasson J. Chem. Soc., Chem. Commun. 1987 1421.
33. J. H. Espenson; Z. Zhu H. T. Zauche J. Org. Chem. 1999 64 1191.
34. U. Bora G. Bose M. Chaudhuri S. Dhar R. Gopinath A. Khan B. Patel Org. Lett. 2000 2 247.
35. L. Yang Z. Lu S. S. Stahl Chem. Commun. 2009 6460.
36. L. Menini J. C. Santos E. V. Gusevskaya Adv. Synth. Catal. 2008 350 2052.
37. G. Zhang R. Liu Q. Xu L. Ma X. Liang Adv. Synth. Catal. 2006 348 862.
38. R. Neumann l. Assael J. Chem. Soc., Chem. Commun. 1988 1285.
39. L. Menini L. A. Parreira E. V. Gusevskaya Tetrahedron Lett. 2007 48 6401.
40. M. J. Earle and S. P. Katdare, World Pat. WO 02/30852, 2002.
41. M. J. Earle S. P. Katdare K. R. Seddon Org. Lett. 2004 6 707.
42. C. Chiappe E. Leandri M. Tebano Green Chem. 2006 8 742.
43. F. Radner J. Org. Chem. 1988 53 3548.
44. M. S. Yusubov V. D. Filimonov H. W. Jin K. W. Chi Bull. Korean Chem. Soc. 1998 19 400.
45. M. Kimura M. Sato T. Murase K. Tsukahara Bull. Chem. Soc. Jpn. 1993 66 2900.