H3PMo12O40 as a new and reusable catalyst for Mukaiyama and Mannich reactions in heterogeneous media

Journal of Molecular Catalysis A: Chemical

Volumn 287, Issue 1-2, 2008, Pages 5-8

  Heydari, Akbar ^a   Khaksar, Samad ^a   Sheykhan, Mehdi ^a   Tajbakhsh, Mahmoud ^b  

^a TARBIAT MODARES UNIVERSITY   (Iran)

^b UNIVERSITY OF MAZANDARAN   (Iran)

Author keywords

hydroxy and amino esters; H3PMo12O40; Keggin type heteropoly acids; Ketene silyl acetal; Mannich reaction; Mukaiyama reaction

Indexed keywords

ALDEHYDES; AMINES; AMINO ACIDS; ESTERS; HYDROGEN INORGANIC COMPOUNDS; REACTION KINETICS;

COUPLING PRODUCTS; IMINES; KETENE SILYL ACETAL; MANNICH REACTIONS; MUKAIYAMA REACTIONS;

CATALYSTS;

EID: 43549124759     PISSN: 13811169     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.molcata.2008.02.024     Document Type: Article

References (32)

1. Anastas P.T., and Warner J.C. In Green Chemistry: Theory and Practice (1998), Oxford Press, Oxford
2. Kozhevnikov I.V. Catal. Rev. Sci. Eng. 37 (1995) 311
3. Kozhevnikov I.V. Chem. Rev. 98 (1998) 171
4. Moffat J.B. In The Surface and Catalytic Properties of Hetropoly Oxometalates (2001), Kluwer, New York
5. Mukaiyama T. Angew. Chem. Int. Ed. 43 (2004) 5590
6. For review, see. Heathcock C.H. In: Trost B.M., Fleming I., and Heathcock C.H. (Eds). Comprehensive Organic Synthesis vol.2 (1991), Pergamon, Oxford, UK 133
7. Kuwajima I., and Nakamura E. J. Am. Chem. Soc. 97 (1975) 3257
8. Kobayashi S., Murakami M., and Mukayama T. Chem. Lett. (1985) 1535
9. Reetz M.T., and Vougioukas A.E. Tetrahedron Lett. 28 (1987) 793
10. Denmark S.E., Winter S.B.D., Su X., and Wong K.T. J. Am. Chem. Soc. 118 (1996) 7404
11. Matsukawa S., Okano N., and Imamoto T. Tetrahedron Lett. 41 (2000) 103
12. Okino T., Hoashi Y., and Takemoto Y. Tetrahedron Lett. 44 (2003) 2817
13. Chen S.-L., Jib S.-J., and Loh T.-P. Tetrahedron Lett. 45 (2004) 375
14. Gaydhankar T.R., Joshi P.N., Kalita P., and Kumar R. J. Mol. Catal. A. Chem. 265 (2007) 306
15. Hagiwara H., Inoguchi H., Fukushima M., Hoshib T., and Suzuki T. Tetrahedron Lett. 47 (2006) 5371
16. Song J.J., Tan Z., Reeves J.T., Yee N.K., and Senanayake C.H. Org. Lett. 9 (2007) 1013
17. Komoto I., and Kobayashi S. Org. Lett. 4 (2002) 1115
18. Lubineau A. J. Org. Chem. 51 (1986) 2142
19. Creger P.L. Tetrahedron Lett. (1972) 79
20. Heydari A., Khaksar S., Akbari J., Esfandyari M., Pourayoubi M., and Tajbakhsh M. Tetrahedron Lett. 48 (2007) 1135
21. Heydari A., Hamadi H., and Pourayoubi M. Catalyst Commun. 8 (2007) 1224
22. Ojima I., Inabe S., and Yoshida K. Tetrahedron Lett. (1977) 3643
23. Guanti G., Narisano E., and Banfi L. Tetrahedron Lett. 28 (1987) 4331
24. Mukaiyama T., Akamatsu H., and Han J.S. Chem. Lett. (1990) 889
25. Mukaiyama T., Kashiwagi K., and Matsui S. Chem. Lett. (1989) 1397
26. Onaka M., Ohno R., Yanagiya N., and Izumi Y. Synlett (1993) 141
27. Ishihara K., Funahashi M., Hanaki N., Miyata M., and Yamamoto H. Synlett (1994) 963
28. Kobayashi S., Mitsuharu A., and Masaru Y. Tetrahedron Lett. 36 (1995) 5773
29. Loh T.P., Feng L.C., and Wei L.L. Tetrahedron 56 (2000) 7309
30. Wang S., Matsumura S., and Toshima K. Tetrahedron Lett. 48 (2007) 6449
31. Loh T.P., and Wei L.L. Tetrahedron Lett. 39 (1998) 323
32. Ollevier S.T., and Nadeau E. Synlett 2 (2006) 219