Use of delaminated zeolites (ITQ-2) and mesoporous molecular sieves in the production of fine chemicals: Preparation of dimethylacetals and tetrahydropyranylation of alcohols and phenols

Journal of Catalysis

Volumn 192, Issue 2, 2000, Pages 441-447

  Rodriguez, I ^a   Climent, M J ^a   Iborra, S ^a   Fornes V ^a   Corma, A ^a  

^a UNIVERSITAT POLITÈCNICA DE VALÈNCIA   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0034631436     PISSN: 00219517     EISSN: None     Source Type: Journal    
DOI: 10.1006/jcat.2000.2861     Document Type: Article

References (56)

1. (a) Bailey, D. C., and Langer, S. H., Chem. Rev. 81, 109 (1981);
2. (b) Corma, A., Chem. Rev. 95, 559 (1995).
3. Balkus, K. J., Jr., Gabrielov, A. G., and Saudler, N., Mater. Res. Soc. Symp. Proc. 368, 359 (1995).
4. Wagner, P., Yoshikawa, M., Lovallo, M., Tsuji, K., Tasptsis, M., and Davis, M. E., Chem. Commun., 2179 (1997).
5. Camblor, M. A., Corma, A., Iborra, S., Miquel, S., Primo, J., and Valencia, S., J. Catal. 172, 76 (1997).
6. Corma, A., Fornes, V., Pergher, S. B., Maesen, Th. L. M., and Buglass, J. G., Nature 376, 353 (1998).
7. Corma, A., Fornes, V., Martinez-Triguero, J., and Pergher, S. B., J. Catal. 186, 57 (1999);
8. Corma, A., Fornés, V., Guil, J. M., Pergher, S., Maesen, Th. L. M., and Buglass, J. G., Micropor. Mesopor. Mater., in press.
9. Greene, T. W., and Wuts, P. G. M., in "Protective Groups in Organic Synthesis," 2nd ed., Chap. 4, pp. 175-210. Wiley, New York, 1991.
10. (a) Evans, M. E., Carbohydr. Res. 21, 4473 (1972);
11. (b) Clode, D. M., Chem. Rev. 79, 491 (1979);
12. (c) Calinaud, P., and Gelas, J., in "Preparation Carbohydrate Chemistry" (S. Hanessian, Ed.), pp. 3-33. Dekker, New York, 1997.
13. (a) Brown, J. J., Lenhard, R. H., and Berstein, S., J. Am. Chem. Soc. 86, 2183 (1964);
14. (b) Li, T. S., Li, S. H., Li, J.-T., and Li, H. Z., J. Chem. Res. Synop., 26 (1997);
15. (c) Matysiak, S., Frank, R., and Pfleiderer, W., Nucleosides Nucleotides 16, 855 (1997).
16. (a) Ashton, M. J., Lawrence, C., Karlsson, J. A., Stuttle, K. A. J., Newton, C. G., Vacher, B. Y. J., Webber, S., and Withnall, M. J., J. Med. Chem. 39, 4888 (1996);
17. (b) Godefroi, E. F., and Meeres, J., U.S. Patent 3,575,999, 1971.
18. Bauer, K., Garbe, D., and Surburg, H., in "Common Fragrances and Flavors Materials," 2nd ed., VCH, Weinheim/New York, 1990.
19. Meskens, F. A. J., Synthesis, 501 (1981).
20. Kamitori, Y., Hojo, M., and Yoshida, T., Tetrahedron Lett. 26, 4767 (1985).
21. Csiba, M., Cleophax, J., Loupy, A., Maltethe, J., and Gero, S. D., Tetrahedron Lett. 59, 333 (1993).
22. Patney, H. K., Synth. Commun. 23, 1523 (1993).
23. Tateiwa, J., Horiuchi, H., and Uemura, S., J. Org. Chem. 60, 4039 (1995).
24. Srkar, A., Yemul, O. S., Bandgar, B. P., Gaikward, N. B., and Wadgaonkar, P. P., Org. Prep. Proc. Int. 28, 613 (1996).
25. Ponde, D., Borate, H. B., Sudalai, A., Ravindranathan, T., and Deshpande, V. H., Tetrahedron Lett. 37, 4605 (1996).
26. Beregszászi, T., and Molnár, A., Synth. Commun. 27, 3705 (1997).
27. Corma, A., Climent, M. J., Garcia, H., and Primo, J., Appl. Catal. 59, 333 (1990).
28. Climent, M. J., Corma, A., Iborra, S., Navarro, M. C., and Primo, J., J. Catal. 161, 783 (1996).
29. Tanaka, Y., Sawamura, N., and Iwamoto, M., Tetrahedron Lett. 39, 9457 (1998).
30. Shibagaki, M., Takahashi, K., Kuno, H., and Matsushita, H., Bull. Chem. Soc. Jpn. 63, 1258 (1990).
31. Taylor, E. C., and Chiang, C. S., Synthesis, 467 (1977).
32. Debal, A., Cuvigny, T., and Larcheveque, M., Synthesis, 391 (1976).
33. Corey, E. J., and Wollenberg, R. H., J. Org. Chem. 40, 2265 (1975).
34. Sonnet, P. E., Synth. Commun. 6, 21 (1976).
35. (a) Hoyer, S., and Laszlo, P., Synthesis, 655 (1986), and references cited therein;
36. (b) Kamaike, K., Ogawa, T., Inoue, Y., and Ishido, Y., Nucleosides Nucleotides 11, 637 (1992);
37. (c) Pietrusiewicz, K. M., Salamonczyk, G. M., Bruzik, K. S., and Wieczorek, W., Tetrahedron 48, 5523 (1992).
38. (a) Van Boom, J. H., Herschied, J. D. M., and Reese, C. B., Synthesis, 169 (1973);
39. (b) Alper, H., and Dinkes, L., Synthesis, 81 (1972).
40. Greene, T. W., and Wuts, P. G. M., in "Protective Groups in Organic Synthesis," 2nd ed., Chap. 4, pp. 31-34. Wiley, New York, 1991.
41. Campelo, J. M., Garcia, A., Lafont, F., Luna, D., and Marinas, J. M., Synth. Commun. 22, 2335 (1992).
42. Bangdar, B. P., Jagtap, S. R., Aghade, B. B., and Wadgaonkar, Synth. Commun. 25, 2211 (1995).
43. Patney, H. K., Synth. Commun. 21, 2329 (1991).
44. Chavez, F., and Godinez, R., Synth. Commun. 22, 159 (1992).
45. Hoyer, S., and Laszlo, P., Synthesis, 655 (1986).
46. Campelo, J. M., Garcia, A., Lafont, F., Luna, D., and Marinas, J. M., Synth. Commun. 24, 1345 (1994).
47. (a) Kumar, P., Dinesh, C. U., Reddy, R. S., and Pandey, B., Synthesis, 1069 (1993);
48. (b) Ballini, R., Bigi, F., Carloni, S., Maggi, R., and Sartori, G., Tetrahedron Lett. 38, 4169 (1997).
49. Kloetstra, K. R., and van Bekkum, H., J. Chem. Res. (S), 26 (1995).
50. Corma, A., Corell, C., Llopis, F., Martinez, A., and Perez-Pariente, J., Appl. Catal. A Gen. 115, 121 (1994).
51. Kresge, C. T., Leonowicz, M. E., Roth, W. J., Vartulli, J. C., and Beck, J. S., Nature 359, 710 (1992).
52. Beck, J. S., Vartulli, J. C., Roth, W. J., Leonowicz, M. E., Kresge, C. T., Schmitt, K. D., Chu, C. T.-W., Olson, D. H., Sheppard, E. W., McCullen, S. B., Higgins, J. B., and Schlenker, J. L., J. Am. Chem. Soc. 114, 10834 (1992).
53. Fajula, F., E.P. 0 488867 A1, 1991.
54. Bellusi, G., Perego, C., Carati, A., Peratello, S., Previde Massara, E., and Perego, G., Stud. Surf. Sci. Catal. 84, 85 (1994).
55. Sastre, G., Catlow, R., and Corma, A., J. Phys. Chem. B 103, 5187 (1999).
56. Emeis, C. A., J. Catal. 141, 347 (1993).