Simple and efficient method for the oxidation of sulfides to sulfones using hydrogen peroxide and a Mo(VI) based catalyst

Catalysis Communications

Volumn 10, Issue 14, 2009, Pages 1948-1951

  Jeyakumar, Kandasamy ^a   Chakravarthy, Rajan Deepan ^a   Chand, Dillip Kumar ^a  

^a INDIAN INSTITUTE OF TECHNOLOGY MADRAS   (India)

Author keywords

Hydrogen peroxide; Molybdenum(VI); Oxidation; Sulfides; Sulfones

Indexed keywords

AMMONIUM HEPTAMOLYBDATE; EFFICIENT METHOD; PROPARGYL; ROOM TEMPERATURE; SULFIDES; SULFONES;

AMMONIUM COMPOUNDS; CYANIDES; ESTERS; FUNCTIONAL GROUPS; HYDROGEN; HYDROGEN PEROXIDE; KETONES; MOLYBDENUM;

OXIDATION;

EID: 68549097786     PISSN: 15667367     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.catcom.2009.07.009     Document Type: Article

References (32)

1. Simpkins N.S. In: Baldwin J.E., and Magnus P.D. (Eds). Sulphones in Organic Synthesis (1993), Pergamon, Oxford
2. Choi S., Yang J.D., Ji M., Choi H., Kee M., Ahn K.H., Byeon S.H., Baik W., and Koo S. J. Org. Chem. 66 (2001) 8192
3. Xu L., Cheng J., and Trudell M.L. J. Org. Chem. 68 (2003) 5388
4. Su W. Tetrahedron Lett. 35 (1994) 4955
5. Beckerbauer R., and Smart B.E. J. Org. Chem. 60 (1995) 6186
6. Shaabani A., Teimouri F., and Lee D.G. Synth. Commun. 33 (2003) 1057
7. Barton D.H.R., Li W., and Smith J.A. Tetrahedron Lett. 39 (1998) 7055
8. Priebe W., and Grynkiewicz G. Tetrahedron Lett. 32 (1991) 7353
9. Baciocchi E., Gerini M.F., and Lapi A. J. Org. Chem. 69 (2004) 3586
10. Prabhu K.R., Devan N., and Chandrasekaran S. Synlett (2002) 1762
11. Khurana J.M., Chauhan S., and Agrawal A. Org. Prep. Proced. Int. 36 (2004) 201
12. Jeyakumar K., and Chand D.K. J. Chem. Sci. 121 (2009) 111
13. Jeyakumar K., and Chand D.K. Tetrahedron Lett. 47 (2006) 4573
14. Khodaei M.M., Baharami K., and Khedri M. Can. J. Chem. 85 (2007) 7
15. Gamelas C.A., Lourenco T., da Costa A.P., Simplicio A.L., Royo B., and Romao C.C. Tetrahedron Lett. 49 (2008) 4708
16. Ismail N., and Rao R.N. Chem. Lett. (2000) 844
17. Mondal E., Bujar Barua P.M., Bose G., and Khan A.T. Chem. Lett. (2002) 210
18. A. Defoin, Synthesis (2004) 706.
19. Ganguly N.C., and Barik S.K. Synthesis (2008) 425
20. Fujisaki S., Fujiwara I., Norisue Y., and Kajigaeshi S. Bull. Chem. Soc. Jpn. 58 (1985) 2429
21. Samanen J.M., and Brandeis E. J. Org. Chem. 53 (1988) 561
22. Ahluwalia V.K., Sharma H.R., and Tyagi R. Tetrahedron 43 (1987) 1141
23. Shukla V.G., Salgaonkar P.D., and Akamanchi K.G. J. Org. Chem. 68 (2003) 5422
24. Kabalka G.W., Yao M.L., Borella S., and Wu Z.Z. Org. Lett. 7 (2005) 2865
25. D'Agostino V.F., Dunn M.J., Ehrlich A.E., and Becker E.I. J. Org. Chem. 23 (1958) 1539
26. Cozzi P.G., and Kotrusz P. J. Am. Chem. Soc. 128 (2006) 4940
27. Bachman G.B., and Carlson C.L. J. Am. Chem. Soc. 73 (1951) 2857
28. Fuller A.T., Tonkin I.M., and Walker J. J. Chem. Soc. (1945) 633
29. Jørgensen K.A. Chem. Rev. 89 (1989) 431
30. Hashemi M.M., and Beni Y.A. J. Chem. Res. (S) (1998) 138
31. Magdziak D., Rodriguez A.A., Van De Water R.W., and Pettus T.R.R. Org. Lett. 4 (2002) 285
32. Saladino R., Neri V., Mincione E., and Filippone P. Tetrahedron 58 (2002) 8493