A catalytic method for synthesis of γ-butyrolactone, ε-caprolactone and 2-cumaranone in the presence of Preyssler's anion, [NaP5W30O110]14-, as a green and reusable catalyst

Journal of Molecular Catalysis A: Chemical

Volumn 252, Issue 1-2, 2006, Pages 90-95

  Bamoharram, Fatemeh F ^a   Heravi, Majid M ^b   Roshani, Mina ^a   Gharib, Ali ^a   Jahangir, Manouchehr ^a  

^a ISLAMIC AZAD UNIVERSITY   (Iran)

^b ALZAHRA UNIVERSITY   (Iran)

Author keywords

Catalyst; Diol; Heteropolyacid; Lactone; Preyssler

Indexed keywords

CATALYSTS; NEGATIVE IONS; RECYCLING; SYNTHESIS (CHEMICAL); THERMAL EFFECTS;

HETEROPOLYACID; LACTONE; PREYSSLER;

CATALYSIS;

EID: 33646493505     PISSN: 13811169     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.molcata.2006.01.067     Document Type: Article

References (56)

1. Raphael R.A., and Ravenscroft P. J. Chem. Soc. Perkin Trans. 1 (1988) 1823
2. Dueholm K.L., and Pederson L.B. Synthesis (1992) 1
3. Robertson D.W., Krushinski J.H., Utterback B.G., and Kauffman R.F. J. Med. Chem. 32 (1989) 1476
4. Bjeldanes L.F. J. Org. Chem. 42 (1977) 2333
5. Weidner-Wells M.A., Decamp A., and Mazzocchi P.H. J. Org. Chem. 54 (1989) 5746
6. Al-Alzemi T.F., Kondaveti L., and Bisht K.S. Macromolecules 35 (2002) 3380
7. Trollasas M., Hedrick J.L., Mecerreyes D., Dubois P., Jerome R., Ihre H., and Hult A. Macromolecules 31 (1998) 2756
8. Lim S.S., Park G.I., Choi J.S., Song In.K., and Lee W.Y. Catal. Today 74 (2002) 299
9. Kajigaeshi S., Nakagawa T., Nagasaki N., and Yamasaki H. Bull. Chem. Soc. Jpn. 59 (1986) 747
10. Hosokawa T., and Murahashi S.I. Heterocycles 33 (1992) 1079
11. Coperet C., Sugihara T., Wu G., Shimayama I., and Negishi E.I. J. Am. Chem. Soc. 117 (1995) 3422
12. El Ali B., and Alper H. J. Org. Chem. 56 (1991) 5357
13. Anastas P.T., and Warner J.C. Green Chemistry, Theory and Practice (1998), Oxford University Press
14. Clark J.H. Green Chem. 1 (1999) 1
15. Hu C., Hashimoto M., Okuhara T., and Misono M. J. Catal. 143 (1993) 437
16. Okuhara T., Kasai A., and Misono M. Shokubai (Catalyst) 22 (1980) 226
17. Yamada T. Peterotech (Tokyo) 13 (1990) 627
18. Okuhara T., Nishimura T., Ohashi K., and Misono M. Chem. Lett. (1990) 1201
19. Okuhara T., Nishimura T., Ohashi K., and Misono M. Chem. Lett. (1995) 155
20. Aoshima A., Tonomura S., and Yamamatsu S. Adv. Technol. 2 (1990) 127
21. Ishii Y., Yoshida T., Yamawaki K., and Ogawa M. J. Org. Chem. 53 (1988) 5549
22. Ishii Y., Yamawaki K., Yoshida T., Ura T., and Ogawa M. J. Org. Chem. 52 (1987) 1868
23. Torok B., Busci I., Beregszaszi T., Kapocsi I., and Molnar A. J. Mol. Catal. 107 (1996) 305
24. Misono M. Mater. Chem. Phys. 17 (1987) 103
25. Okuhara T., Mizuno N., and Misono M. Adv. Catal. 41 (1996) 113
26. Hayashi H., and Moffat J.B. J. Catal. 81 (1983) 66
27. Mizuno N., and Misono M. Chem. Rev. 98 (1998) 199
28. Hill C.L., and Prosser-McCartha C.M. Coord. Chem. Rev. 143 (1995) 407
29. Alizadeh M.H., Harmalker S.P., Jeannin Y., Martin-Frere J., and Pope M.T. J. Am. Chem. Soc. 107 (1985) 2662
30. Alizadeh M.H., Razavi H., Farrash Bamoharram F., and Hassanzadeh M.H. Kinet. Catal. 44 (2003) 524
31. Bamoharram F.F., Heravi M.M., Roshani M., Jahangir M., and Gharib A. Appl. Catal. 302 (2006) 42
32. F.F. Bamoharram, M.M. Heravi, M. Roshani, M. Jahangir, A. Gharib, J. Mol. Catal. (2006), submitted for publication.
33. F.F. Bamoharram, M. Roshani, M.H. Alizadeh, M. Moghayadee, J. Braz. Chem. Soc. (2006), in press.
34. Alizadeh M.H., Razavi H., Bamoharram F.F., and Daneshvar K. J. Mol. Catal. 206 (2003) 89
35. Heravi M.M., Derikvand F., and Bamoharram F.F. J. Mol. Catal. 242 (2005) 173
36. M.M. Heravi, Kh. Bakhtiari, F.F. Bamoharram, Catal. Commun. (2006), in press.
37. M.M. Heravi, R. Motamedi, N. Seifi, F.F. Bamoharram, J. Mol. Cat. (2006), in press.
38. Kozhevnikov I.V. Chem. Rev. 98 (1998) 171
39. Ballini R., Marcantoni E., and Petrini M. Tetrahedron Lett. 33 (1992) 4835
40. Astudillo L., Galindo A., Gonzalez A.G., and Mansilla H. Heterocycles 36 (1993) 1075
41. Balicki R. Synth. Commun. 29 (1999) 2235
42. Varma R.S., and Naicker K.P. Org. Lett. 1 (1999) 189
43. Heaney H., and Newbold A.J. Tetrahedron Lett. 42 (2001) 6607
44. Pietikainen P. J. Mol. Catal. 165 (2001) 73
45. Kureshy R.I., Khan N.H., Abdi S.H.R., Patel S.T., and Jasra R.V. Tetrahedron: Asymmetry 12 (2001) 433
46. Damavandi J.A., Karami B., and Zolfigol M.A. Synlett (2002) 933
47. Kelly D.R., and Roberts S.M. Pept. Sci. 84 (2006) 74
48. Laha S.C., and Kumar R. J. Catal. 204 (2001) 64
49. Adam W., Shaha-Moller C.R., and Schmid K.S. J. Org. Chem. 66 (2001) 7365
50. Omar Bouh A., and Espenson J.H. J. Mol. Catal. 200 (2003) 43
51. Karami B., Montazerozohori M., Moghadam M., Habibi M.H., and Niknam K. Turk. J. Chem. 29 (2005) 539
52. Carno S., Do N.M., and Sieser J.E. Tetrahedron Lett. 41 (2000) 2299
53. Gonsalves A.M.A.R., Johnstone R.A.W., Pereira M.M., and Shaw J. J. Chem. Res. (S) (1991) 208
54. Lu C.S., Hughes E.W., and Giguere P.A. J. Am. Chem. Soc. 63 (1941) 1507
55. Dobado J.A., Molina J., and Portal D. J. Phys. Chem. A 102 (1998) 778
56. Kozhevnikov I.V. Russ. Chem. Rev. (English translation) 56 (1987) 811