J IRAN CHEM SOC (2012) 9:1015–1019
1019
16. Z. Jin, P.C. Vandort, P.L. Fuchs, Phosphorus. Sulfur Silicon
Relat. Elem. 95, 1–4 (1994)
17. W.H.O. Zhu G-D, Chem. Rev. 95, 1877–1952 (1995)
18. M.H. Ali, G.J. Bohnert, Synthesis, 1238–1240 (1998)
19. D.H.R. Barton, W. Li, J.A. Smith, Tetrahedron Lett. 39,
7055–7058 (1998)
20. F. Gregori, I. Nobili, F. Bigi, R. Maggi, G. Predieri, G. Sartori, J.
Mol. Catal. A Chem. 286, 124–127 (2008)
21. N. Iranpoor, D. Mohajer, A.-R. Rezaeifard, Tetrahedron Lett. 45,
3811–3815 (2004)
and also non-cationic conditions, the biphasic system has a
reduced reaction time and requires less hydrogen peroxide.
Acknowledgments We gratefully acknowledge the partial financial
support from the Research Affairs Division Isfahan University of
Technology (IUT), Isfahan. Further partial financial support of Iran
Nanotechnology Initiative Council (INIC), National Elite Foundation
(NEF) and Center of Excellency in Sensors and Green Chemistry
(IUT) is also gratefully acknowledged.
22. J.M. Khurana, A.K. Panda, A. Ray, A. Gogia, Org. Prep. Proced.
Int. 28, 234–237 (1996)
23. P.J. Kropp, G.W. Breton, J.D. Fields, J.C. Tung, B.R. Loomis, J.
Am. Chem. Soc. 122, 4280–4285 (2000)
References
24. K.R. Roh, K.S. Kim, Y.H. Kim, Tetrahedron Lett. 32, 793–796
(1991)
25. X.-Y. Shi, J.-F. Wei, J. Mol. Catal. A Chem. 280, 142–147 (2008)
26. M. Bandini, P.G. Cozzi, A. Umani-Ronchi, Chem. Commun.
919–927 (2002)
1. J.-H. Fuhrhop, G. Li, E.J. Corey, Organic synthesis: concepts and
methods (Wiley, New York, 2003)
2. P. Kelly, S.E. Lawrence, A.R. Maguire, Synlett, 1501–1506
(2007)
3. A.Y. Koposov, V.V. Zhdankin, Synthesis, 22–24 (2005)
4. W. Qian, L. Pei, Synlett 709–712 (2006)
5. R.S. Varma, R.K. Saini, H.M. Meshram, Tetrahedron Lett. 38,
6525–6528 (1997)
6. B. Karimi, M. Ghoreishi-Nezhad, J.H. Clark, Org. Lett. 7,
625–628 (2005)
7. M. Mba, L.J. Prins, G. Licini, Org. Lett. 9, 21–24 (2006)
8. K. Sato, M. Hyodo, M. Aoki, X.-Q. Zheng, R. Noyori, Tetrahe-
dron 57, 2469–2476 (2001)
9. W.L. Xu, Y.Z. Li, Q.S. Zhang, H.S. Zhu, Synthesis, 227–232
(2004)
10. M.M. Dell’Anna, P. Mastrorilli, C.F. Nobile, J. Mol. Catal. A:
Chem. 108, 57–62 (1996)
11. B.G.A.D.D.A.G. Martin S F, Tetrahedron, 53 8997–9006 (1997)
12. A. Bravo, B. Dordi, F. Fontana, F. Minisci, The. J. Org. Chem.
66, 3232–3234 (2001)
27. E.M. McGarrigle, D.G. Gilheany, Chem. Rev. 105, 1563–1602
(2005)
28. Y.N. Belokon, M. North, V.I. Maleev, N.V. Voskoboev, M.A.
Moskalenko, A.S. Peregudov, A.V. Dmitriev, N.S. Ikonnikov,
H.B. Kagan, Angew. Chem. Int. Ed. 43, 4085–4089 (2004)
29. D. Feichtinger, D.A. Plattner, Angew. Chem. Int. Ed. 36,
1718–1719 (1997)
30. X. Zheng, C.W. Jones, M. Weck, J. Am. Chem. Soc. 129,
1105–1122 (2007)
31. A. Abdolmaleki, S. Malek-Ahmadi, Can. J. Chem. 89,
1202–1206 (2011)
32. J.E. Barker, T. Ren, Tetrahedron Lett. 45, 4681–4683 (2004)
33. J.E. Barker, T. Ren, Tetrahedron Lett. 46, 6805–6808 (2005)
34. X.-M. Feng, Z. Wang, N.-S. Bian, Z.-L. Wang, Inorg. Chim. Acta
360, 4103–4110 (2007)
35. D.E. De Vos, T. Bein, J. Organomet. Chem. 520, 195–200 (1996)
36. A.A. Belal, P. Chaudhuri, I. Fallis, L.J. Farrugia, R. Hartung,
N.M. McDonald, B. Nuber, R.D. Peacock, J. Weiss, K. Wieg-
hardt, Inorg. Chem. 30, 4397–4402 (1991)
13. G. Kar, A.K. Saikia, U. Bora, S.K. Dehury, M.K. Chaudhuri,
Tetrahedron Lett. 44, 4503–4505 (2003)
14. M. Palucki, P. Hanson, E.N. Jacobsen, Tetrahedron Lett. 33,
7111–7114 (1992)
15. K. Fujiki, S. Akieda, H. Yasuda, Y. Sasaki, Synthesis, 1034–1042
(2001)
123