The efficient and chemoselective MoO3-catalyzed oxidation of sulfides to sulfoxides and sulfones with H2O2

Canadian Journal of Chemistry

Volumn 85, Issue 1, 2007, Pages 7-11

  Khodaei, Mohammad Mehdi ^a   Bahrami, Kiumars ^a   Khedri, Mohammad ^a  

^a RAZI UNIVERSITY   (Iran)

Author keywords

H2O2 MoO 3 system; Oxidation; Sulfides; Sulfones; Sulfoxides

Indexed keywords

CATALYTIC OXIDATION; ETHANOL; FUNCTIONAL GROUPS; HYDROGEN PEROXIDE; MOLYBDENUM COMPOUNDS; REACTION RATES;

CHEMOSELECTIVE OXIDATION; REACTION TIMES; SULFONES; SULFOXIDES;

SULFUR COMPOUNDS;

EID: 34247885886     PISSN: 00084042     EISSN: None     Source Type: Journal    
DOI: 10.1139/V06-177     Document Type: Article

References (32)

1. M. Hudlicky. Oxidation in organic chemistry. ACS Monograph Ser. 186. American Chemical Society, Washington, DC. 1990. p. 252.
2. J. Drabowski, P. Kielbasinski, and M. Mikolajczyk. Synthesis of Sulfoxides. John Wiley and Sons, New York. 1994.
3. S. Pati and Z. Rappoport. The synthesis of sulphones, sulphoxides, and cyclic sulphides. John Wiley and Sons, New York. 1994.
4. R.S. Varma, R.K. Saini, and H.M. Meshram. Tetrahedron Lett. 38, 6525 (1997).
5. G.W. Gokel, H.M. Gerdes, and D.M. Dishong. J. Org. Chem. 45, 3634 (1980).
6. W. Adam and L. Hadjiarapoglou. Tetrahedron Lett. 33, 469 (1992).
7. Y. Ishii, H. Tanaka, and Y. Nishiyama. Chem. Lett. 1 (1994).
8. C.G. Venier, T.G. Squires, Y.-Y. Chen, G.P. Hussmann, J.C. Shei, and B.F. Smith. J. Org. Chem. 47, 3773 (1982).
9. A. McKillop and J.A. Tarbin. Tetrahedron Lett. 24, 1505 (1983).
10. R.P. Greenhalgh. Synlett, 235 (1992).
11. S. Yamazaki. Bull. Chem. Soc. Jpn. 69, 2955 (1996).
12. R.S. Varma, R.K. Saini, and H.M. Meshram. Tetrahedron Lett. 38, 6525 (1997).
13. B.M. Choudary, B. Bharathi, C.V. Reddy, and M.L. Kantam. J. Chem. Soc. Perkin Trans. 1, 2069 (2002).
14. D. Bethell, P.C.B. Page, and H. Vahedi. J. Org. Chem. 65, 6756 (2000).
15. K. Yazu, T. Furuya, K. Miki, and K. Ukegawa. Chem. Lett. 32, 920 (2003).
16. M. Matteucci, G. Bhalay, and M. Braley. Org. Lett. 5, 235 (2003).
17. B. Yadollahi. Chem. Lett, 32, 1066 (2003).
18. E. Baciocchi, M. Francesca Gerini, and A. Lapi. J. Org. Chem. 69, 3586 (2004).
19. Y.-C. Jeong, S. Choi, Y.D. Hwang, and K.-H. Ahn. Tetrahedron Lett. 45, 9249 (2004).
20. S. Velusamy, A. V. Kumar, R. Saini, and T. Punniyamurthy. Tetrahedron Lett. 46, 3819 (2005).
21. K. Kaczorowska, Z. Kolarska, M. Katarzyna, and P. Kowalski. Tetrahedron, 61, 8315 (2005).
22. K. Bahrami. Tetrahedron Lett. 47, 2009 (2006).
23. J.R. Lindsay Smith, J. Murray, P.H. Walton, and T.R. Lowdon. Tetrahedron Lett. 47, 2005 (2006).
24. F. Hossienpoor and H. Golchoubian. Tetrahedron Lett. 47, 5195 (2006).
25. S. Velusamy, A.V. Kumar, R. Saini, and T. Punniyamurthy. Tetrahedron Lett. 46, 3819 (2005).
26. J. Drabowicz and M. Mikolajczyk. Synthesis, 758 (1978).
27. M.M. Khodaei, P. Salehi, and M. Goodarzi. Synth. Commun. 31, 1253 (2001).
28. P. Salehi, M.M. Khodaei, and M. Goodarzi. Synth. Commun. 32, 1259 (2002).
29. P. Salehi, M.M. Khodaei, and M. Goodarzi. Russ. J. Org. Chem. 392 (2002).
30. G.P. Romanelli, P.G. Vazquez, and P. Tundo. Synlett, 75 (2005).
31. K. Jeyakumar and D.K. Chand. Tetrahedron Lett. 47, 4573 (2006).
32. Y. Sasaki, K. Ushimarou, K. Iteya, H. Nakayama, S. Yamaguchi, and J. Ichihara. Tetrahedron Lett. 45, 9513 (2004).