Direct one-pot synthesis of β-hydroxysulfides from terminal olefins in a mixture of [bmim][BF4] and water in presence of molecular oxygen

Journal of Molecular Catalysis A: Chemical

Volumn 272, Issue 1-2, 2007, Pages 26-30

  Kamal, Ahmed ^a   Reddy, D Rajasekhar ^a   Rajendar, ^a  

^a INDIAN INSTITUTE OF CHEMICAL TECHNOLOGY   (India)

Author keywords

Hydroxysulfides; Alkenes; Ionic liquid

Indexed keywords

CATALYST ACTIVITY; FUNCTIONAL GROUPS; IONIC LIQUIDS; MOLECULAR OXYGEN; OLEFINS; SYNTHESIS (CHEMICAL);

BASE CATALYSTS; HYDROXYSULFIDES; THIOPHENOLS;

SULFUR COMPOUNDS;

EID: 34249319802     PISSN: 13811169     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.molcata.2007.03.014     Document Type: Article

References (41)

1. Francesco F., Ferdinando P., Simone T., and Luigi V. J. Org. Chem. 68 (2003) 8248 and references therein
2. Luly J.R., Yi N., Soderquist J., Stein H., Cohen J., Perun T.J., and Plattner J.J. J. Med. Chem. 30 (1987) 1609
3. Corey E.J., Clark D.A., Goto G., Marfat A., Mioskowski C., Samuelsson B., and Hammarstrom S. J. Am. Chem. Soc. 102 (1980) 3663
4. Peach M.E. In: Patai S. (Ed). The Chemistry of the Thiol Group (1974), John Wiley, New York 771 (Part 3)
5. Iida T., Yamamoto N., Sasai H., and Shibasaki M. J. Am. Chem. Soc. 119 (1997) 4783
6. Fringuelli F., Pizzo F., Tortoioli S., and Vassaro L. J. Org. Chem. 68 (2003) 8248
7. Fringuelli F., Pizzo F., Tortoioli S., and Vassaro L. J. Org. Chem. 69 (2004) 8780
8. Pironti V., and Colonna S. Green Chem. 7 (2005) 43
9. Yadav J.S., Reddy B.V.S., and Gakul B. Chem. Lett. (2002) 906 references therein
10. Beckwith A.L.J., and Wagner R.D. J. Org. Chem. 46 (1981) 3638 references therein
11. Subbareddy K., Arumugam S., and Brian C.B. Tetrahedron Lett. 42 (2001) 3791
12. Belly M., and Zamboni R. J. Org. Chem. 54 (1989) 1230
13. Pradeep K., Rajesh K.P., and Vishnumurthy R.H. Synlett (1999) 1921
14. Anderson L.L., Arnold J., and Bergman R.G. J. Am. Chem. Soc. 127 (2005) 14542
15. Waser J., Naambu H., and Carreira E.M. J. Am. Chem. Soc. 127 (2005) 8294
16. Karshtedt D., Bell A.T., and Tilley T.D. J. Am. Chem. Soc. 127 (2005) 12640
17. Yang C.-G., and He C. J. Am. Chem. Soc. 127 (2005) 6966
18. Talluri S.K., and Sudalai A. Org. Lett. 7 (2005) 855
19. Hall N. Science 266 (1994) 32
20. Tietze L.F., and Haunet F. In: Vogtle F., Stoddart J.F., and Shibasaki M. (Eds). Stimulating Concepts in Chemistry (2000), Wiley-VCH, Weinheim 39
21. Welton T. Chem. Rev. 99 (1999) 2071
22. Wasserscheid P., and Keim W. Angew. Chem., Int. Ed. 39 (2000) 3772
23. Wilkes J.S. Green Chem. 4 (2002) 73
24. Wasserscheid P., and Welton T. Ionic Liquids in Synthesis (2003), Wiley-VCH, Weinheim, Germany
25. Jain N., Kumar A., Chauhan S., and Chouhan S.M.S. Tetrahedron 61 (2005) 1015
26. Ansari I.A., Joyasawal S., Gupta M.K., Yadav J.S., and Gree R. Tetrahedron Lett. 46 (2005) 7507
27. Fraga-Dubreuil J., and Bazureau J.P. Tetrahedron Lett. 42 (2001) 6097
28. Fraga-Dubreuil J., and Bazureau J.P. Tetrahedron 59 (2003) 6121
29. Handy S.T., and Okello M. Tetrahedron Lett. 44 (2003) 8399
30. Hakkou H., Vanden Eynde J.J., Bazureau J.P., and Hamelin J. Tetrahedron 60 (2004) 3745
31. Miao W., and Chan T.H. Org. Lett. 5 (2003) 5003
32. Anjaiah S., Chandrasekhar S., and Gree R. Tetrahedron Lett. 45 (2004) 569
33. de Kort M., Tuin A.W., Kuiper S., Overkleeft H.S., van der Marel G.A., and Buijsman R.C. Tetrahedron Lett. 45 (2004) 2171
34. Legeay J.-C., Vanden Eynde J.J., and Bazureau J.P. Tetrahedron 61 (2005) 12386
35. Miao W.S., and Chan T.H. J. Org. Chem. 70 (2005) 3251
36. Kamal A., and Chouhan G. Tetrahedron Lett. 44 (2003) 3337
37. Kamal A., and Chouhan G. Tetrahedron Lett. 45 (2004) 8801
38. Kamal A., and Chouhan G. Tetrahedron Lett. 46 (2005) 1489
39. Kamal A., Ramu R., Azhar M.A., and Khanna G.B. Tetrahedron Lett. 46 (2005) 2675
40. Placzek T.A., Donelson L.J., Trivedi R., Gibbs R.A., and De S.K. Tetrahedron Lett. 46 (2005) 9029
41. Surendra K., Krishnaveni N.S., Nageswar Y.V.D., and Rao K.R. J. Org. Chem. 68 (2003) 4994