Ionic liquid mediated efficient reduction of nitroarenes using stannous chloride under sonication

Tetrahedron Letters

Volumn 46, Issue 23, 2005, Pages 3987-3990

  Rai, Ganesha ^a   Jae, Min Jeong ^a,b   Lee, Yun Sang ^a   Hyung, Woo Kim ^a   Dong, Soo Lee ^a   Chung, June Key ^a,b   Myung, Chul Lee ^a  

^a Seoul National University Hospital   (South Korea)

^b Seoul National University   (South Korea)

Author keywords

Ionic liquid; Reduction of nitroarene; Sonication; Stannous chloride

Indexed keywords

AROMATIC AMINE; AROMATIC NITRO COMPOUND; ION; STANNOUS CHLORIDE;

ARTICLE; CHEMICAL REACTION KINETICS; LIQUID; PRODUCTIVITY; RECYCLING; REDUCTION; ULTRASOUND;

EID: 18844407050     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2005.04.035     Document Type: Article

References (42)

1. R. Ehernkanfer, and S. Ram Tetrahedron Lett. 25 1984 3415 and references cited therein
2. For some recent reports see: C. Zhang, Y. Wang, and J.Y. Wang J. Chin. Chem. Soc. 51 3 2004 569
3. S.K. Mohapatra, S.U. Sonavane, R.V. Jayaram, and P. Selvam Appl. Catal. B 46 1 2003 155
4. W. Lei, L. Pinhua, W. Zongtao, Y. Jincan, W. Min, and D. Yanbin Synthesis 2003 2001
5. S.K. Mohapatra, S.U. Sonavane, R.V. Jayaram, and P. Selvam Org. Lett. 4 24 2002 4297
6. A. Vass, J. Dudas, J. Toth, and R.S. Varma Tetrahedron Lett. 42 32 2001 5347
7. M.R. Pitts, J.R. Harrison, and C.J. Moody J. Chem. Soc., Perkin Trans. 1 2001 955 and references cited therein
8. T. Tsukinoki, and H. Tsuzuki Green Chem. 3 1 2001 37
9. C. Yu, B. Liu, and L. Hu J. Org. Chem. 66 3 2001 919
10. A. Yasuhara, A. Kasano, and T. Sakamoto J. Org. Chem. 64 7 1999 2301 and references therein
11. C.J. Moody, and M.R. Pitts Synlett 1998 1028
12. R.A. Sheldon Chem. Commun. 2001 2399
13. J. Dupont, R.F. de Souza, and P.A.Z. Suarez Chem. Rev. 102 2002 3667
14. For some recent examples see: C.M. Gordon Appl. Catal. A 222 2001 101
15. G. Zhao, T. Jiang, H. Gao, B. Han, J. Huang, and D. Sun Green Chem. 2004 75
16. M. Hasegawa, H. Ishii, and T. Fuchigami Green Chem. 2003 512
17. K. Qiao, and Y. Deng New J. Chem. 2002 667
18. V.K. Aggarwal, I. Emme, and A. Mereu Chem. Commun. 2002 1612
19. V.L. Boulaire, and R. Grée Chem. Commun. 2000 2195
20. M. Smietana, and C. Mioskowski Org. Lett. 3 7 2001 1037
21. A. Kumar, and S.S. Pawar J. Org. Chem. 69 4 2004 19
22. For recent reviews, see: T. Welton Chem. Rev. 99 1999 2071
23. P. Wasserscheid, and W. Keim Angew. Chem. Int. Ed. 39 2000 3772
24. R.A. Sheldon Chem. Commun. 2001 2399
25. H. Zhao, and S.V. Malhotra Aldrichim. Acta 35 3 2002 75
26. U. Kragl, M. Eckstein, and N. Kaftzik Curr. Opin. Biotechnol. 13 2002 565
27. J.K. Lee, and M.J. Kim J. Org. Chem. 67 19 2002 6845
28. J.G. Huddleston, H.D. Willauer, R.P. Swatloski, A.E. Visser, and R.D. Rogers Chem. Commun. 1998 1765
29. K.A. Srinivas, A. Kumar, and S.M.S. Chauhan Chem. Commun. 2002 2456
30. H. Waffenschimidt, and P. Wasserscheid J. Mol. Catal. A 164 2000 61
31. D.W. Kim, C.E. Song, and D.Y. Chi J. Am. Chem. Soc. 124 2002 10278
32. H.W. Kim, J.M. Jeong, Y.-S. Lee, D.Y. Chi, K.-H. Chung, D.S. Lee, J.-K. Chung, and M.C. Lee Appl. Radiat. Isot. 61 2004 1242
33. F.A. Khan, J. Dash, C. Sudheer, and R.K. Gupta Tetrahedron Lett. 44 2003 7783
34. X.L. Zheng, and Y.M. Zhang Chin. J. Chem. 20 2002 925
35. F.D. Bellamy, and K. Ou Tetrahedron Lett. 25 8 1984 839
36. T. Satoh Ventron Alembic 14 1978 3
37. K.S. Suslick, D.A. Hammerton, and R. Cline J. Am. Chem. Soc. 108 1986 5641
38. T. Mason Chem. Soc. Rev. 26 1997 443
39. For some recent examples see S.D. Lepore, and Y. He J. Org. Chem. 68 21 2003 8261
40. J.S. Yadav, B.V.S. Reddy, K.B. Reddy, K.S. Raj, and A.R. Prasad J. Chem. Soc., Perkin Trans. 1 2001 1939
41. S. Streiff, N. Ribeiro, and L. Desaubry Chem. Commun. 2004 346
42. B.C. Ranu, and A. Das Tetrahedron Lett. 45 2004 6875