Catalytic oxidative cleavage of terminal olefins by chromium(III) stearate

Journal of Molecular Catalysis A: Chemical

Volumn 270, Issue 1-2, 2007, Pages 289-294

  Jarupinthusophon, Suekanya ^a   Thong In, Uthumporn ^a   Chavasiri, Warinthorn ^a  

^a CHULALONGKORN UNIVERSITY   (Thailand)

Author keywords

Chromium(III) stearate; Homogeneous catalysis; Oxidative cleavage; Terminal olefins

Indexed keywords

CATALYTIC OXIDATION; CHEMICAL BONDS; CHROMIUM COMPOUNDS; DERIVATIVES; REACTION KINETICS; THERMAL EFFECTS;

CHROMIUM STEARATE; HOMOGENEOUS CATALYSIS; OXIDATIVE CLEAVAGES; TERMINAL OLEFINS;

OLEFINS;

EID: 34247272037     PISSN: 13811169     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.molcata.2007.02.007     Document Type: Article

References (49)

1. Haines A.H. Methods for the Oxidation of Organic Compounds (1985), Academic Press, New York
2. Lee D.G., and Chen T. In: Trost B.M., and Fleming I. (Eds). Comprehensive Organic Synthesis. 1st ed. vol. 7 (1991), Pergamon Press, Oxford 541-591
3. Barton D.H.R., Chern C., and Jaszberenyi J. Tetrahedron 51 (1995) 1867-1886
4. Yates M.H. Tetrahedron Lett. 38 (1997) 2813-2816
5. Baucherel X., Uziel J., and Juge S. J. Org. Chem. 66 (2001) 4504-4510
6. Lin Y.H., Williams I.D., and Li P. Appl. Catal. A 150 (1997) 221-229
7. Tokunaga M., Aoyama H., Shirogane Y., Obora Y., and Tsuji Y. Catal. Today 117 (2006) 138-140
8. Xing D., Guan B., Cai G., Fang Z., Yang L., and Shi Z. Org. Lett. 8 (2006) 693-696
9. Ley S.V., Ramarao C., Lee A.-L., Ostergaard N., Smith S.C., and Shirley I.M. Org. Lett. 5 (2003) 185-187
10. Yu W., Mei Y., Kang Y., Hua Z., and Jin Z. Org. Lett. 6 (2004) 3217-3219
11. Choudary B.M., and Reddy P.N. J. Mol. Catal. A 103 (1995) L1-L3
12. Drago R.S., Corden B.B., and Barnes C.W. J. Am. Chem. Soc. 108 (1986) 2453-2454
13. Antonelli E., D'Aloisio R., Gambaro M., Fiorani T., and Venturello C. J. Org. Chem. 63 (1998) 7190-7206
14. Neumann R., and Abu-Gnim C. J. Am. Chem. Soc. 112 (1990) 6025-6031
15. Whitehead D.C., Travis B.R., and Borhan B. Tetrahedron Lett. 47 (2006) 3797-3800
16. Hanessian S. Total Synthesis of Natural Product: The Chiron Approach (1983), Pergamon Press, New York (Chapter 2)
17. Spindler F., Pittelkow U., and Blaser H.U. Chirality 3 (1991) 370-375
18. Blaser H.U., Jalett H.P., and Spindler F. J. Mol. Catal. A 107 (1996) 85-94
19. Ray P.H., Kelsey J.E., Bigham E.C., Benedict C.D., and Miller T.A. Bacterial Lipopolysacharides (1983), ACS, Washington, DC
20. Cooper A.J.L., Ginos J.Z., and Meister A. Chem. Rev. 83 (1983) 321-358
21. Taber D.F., and Nakajima K. J. Org. Chem. 70 (2001) 2515-2517
22. Miller K.M., Huang W.-S., and Jamison T.F. J. Am. Chem. Soc. 125 (2003) 3442-3443
23. Pappas A.J.J., Keaveney W.P., Gancher E., and Berger M. Tetrahedron Lett. 36 (1966) 4273-4274
24. Lee D.G., Chen T., and Wang Z. J. Org. Chem. 58 (1993) 2918-2919
25. Joshi P.L., and Hazra B.G. J. Chem. Res., Synop. (2000) 38-39
26. Bonini C., Chiummiento L., Funicello M., Lupattel P., and Pullez M. Eur. J. Org. Chem. (2006) 80-83
27. Travis B.R., Narayan R.S., and Borhan B. J. Am. Chem. Soc. 124 (2002) 3824-3825
28. Schomaker J.M., Travis B.R., and Borhan B. Org. Lett. 5 (2003) 3089-3092
29. Molander G.A., and Figueroa R. Org. Lett. 8 (2006) 75-78
30. Carlsen P.H.J., Katsuki T., Martin V.S., and Sharpless K.B. J. Org. Chem. 46 (1981) 3936-3938
31. Torii S., Inokuchi T., and Kondo K. J. Org. Chem. 50 (1985) 4980-4982
32. Plietker B. J. Org. Chem. 68 (2003) 7123-7125
33. Frunzke J., Loschen C., and Frenking G. J. Am. Chem. Soc. 126 (2004) 3642-3652
34. Rao Y.V.S., Rani S.S., and Choudary B.M. J. Mol. Catal. 75 (1992) 141-146
35. Herrmann W.A., Weskamp T., Zoller J.P., and Fischer R.W. J. Mol. Catal. A 153 (2000) 49-52
36. Brooks C.D., Huang L.C., McCarron M., and Johnstone R.A.W. Chem. Commun. (1999) 37-38
37. Yang D., and Zhang C. J. Org. Chem. 66 (2001) 4814-4818
38. Muzart J. Chem. Rev. 92 (1992) 113-140
39. Bukowski W. J. Mol. Liq. 111 (2004) 47-52
40. Kanemoto S., Saimoto H., Oshima K., and Nozaki H. Tetrahedron Lett. 25 (1984) 3317-3320
41. Tolman C.A., Druliner J.D., Krusic P.J., Nappa M.J., Seidel W., Williams I.D., and Ittel S.D. J. Mol. Catal. 48 (1988) 129-148
42. Freeman F., DuBois R.H., and Yamachika N.J. Tetrahedron 25 (1969) 3441-3446
43. Rentea C.N., Necsoiu I., Rentes M., Ghenciulescu A., and Nenitzescu C.D. Tetrahedron 22 (1966) 3501-3513
44. Freeman F., and Arledge K.W. J. Org. Chem. 37 (1972) 2656-2662
45. Mosher W.A., Steffgen F.W., and Lansbury P.T. J. Org. Chem. 26 (1961) 670-679
46. Haynes N.B., Redmore D., and Timmons C.J. J. Chem. Soc. (1963) 2420-2422
47. Kirk-Othmer, Encyclopedia of Chemical Technology, 2nd ed., 1968.
48. Ohsugi S., Nishide K., and Node M. Tetrahedron 59 (2003) 1859-1871
49. Barton D.H.R., Lee K.W., Mehl W., Ozbalik N., and Zhang L. Tetrahedron 46 (1990) 3753-3768