Heteropoly acids as useful recyclable heterogeneous catalysts for the facile and highly efficient aza-cope rearrangement of N-allylanilines

Applied Catalysis A: General

Volumn 359, Issue 1-2, 2009, Pages 84-87

  Chaskar, Atul ^a,b   Padalkar, Vikas ^a   Phatangare, Kiran ^a   Patil, Ketan ^a   Bodkhe, Akalpita ^a   Langi, Bhushan ^a  

^a C K Thakur Research Centre   (India)

^b POLITECNICO DI MILANO   (Italy)

Author keywords

Aza cope rearrangement; Heteropoly acid; Ionic liquid

Indexed keywords

AMBIENT CONDITIONS; AZA-COPE REARRANGEMENT; HETEROGENEOUS CATALYSTS; HETEROPOLY ACID; HIGH YIELDS; LIQUID REACTIONS; PHOSPHOMOLYBDIC ACIDS; REACTION MEDIAS; REACTION TIME; SHORT REACTION TIME;

CATALYSIS; CATALYST ACTIVITY; IONIZATION OF LIQUIDS; IONS; MOLYBDENUM; ORGANIC SOLVENTS; SULFUR COMPOUNDS;

IONIC LIQUIDS;

EID: 64149113294     PISSN: 0926860X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.apcata.2009.02.031     Document Type: Article

References (26)

1. Lutz R.P. Chem. Rev. 84 (1984) 205-247
2. Rhoads S.J., and Raulins N.R. Org. React. 22 (1975) 1-252
3. Bennett G.B. Synthesis (1977) 589-606
4. Blechert S. Synthesis (1989) 71-82
5. Marcinkiewicz S., Green J., and Mamalis P. Tetrahedron 14 (1961) 208-222
6. Jolidon S., and Hansen H.J. Helv. Chim. Acta 60 (1977) 978-1032
7. Bailey P.D., and Harrison M.J. Tetrahedron Lett. 30 (1989) 5341-5344
8. Barta N.S., Cook G.R., Landis M.S., and Stille J.R. J. Org. Chem. 57 (1992) 7188-7194
9. Canahan F.L., and Hurd C.D. J. Am. Chem. Soc. 52 (1930) 4586-4595
10. Saito A. Yakugaku Zasshi 128 (2008) 1133-1138
11. Saito A., Kanno A., and Hanzawa Y. Angew. Chem. Int. Ed. 46 (2007) 3931-3933
12. Jain S., Pandey N., and Kishore D. Indian J. Chem. 46B (2007) 529-531
13. Jain S., Pandey N., and Kishore D. J. Indian Chem. Soc. 83 (2006) 1052-1054
14. Jain S., Pandey N., and Kishore D. J. Indian Chem. Soc. 83 (2006) 938-940
15. Gomez A., Sandra L., Stashenko E., Palma A., Bahsas A., and Amaro-Luis J. Synlett (2006) 2275-2277
16. Palma A., Barajas J., Kouznetsov V., Vladimir V., Stashenko E., Bahsas A., and Amaro-Luis J. Synlett (2004) 2721-2724
17. Cooper M.A., Lucas M.A., Taylor J.M., Ward A.D., and Williamson N.M. Synthesis (2001) 621-625
18. Bader A.R., Bridgwater R.J., and Freeman P.R. J. Am. Chem. Soc. 83 (1961) 3319-3323
19. Krowicki K., Paillous N., Riviere M., and Lattes A.J. J. Heterocycl. Chem. 13 (1976) 555-560
20. Hyre J.E., and Bader A.R. J. Am. Chem. Soc. 80 (1958) 437-439
21. Okuhara T., Mizuno N., and Misono M. Adv. Catal. 41 (1996) 113-252
22. Tiofeeva M.N., Dimidov A.V., and Kozhevnikov I.V. J. Mol. Catal. 79 (1993) 21-28
23. Drago R.S., Dias J.A., and Maier T. J. Am. Chem. Soc. 119 (1997) 7702-7710
24. Schwegler M.A., van Bekkum H., and Munck N. Appl. Catal. 74 (1991) 191-204
25. Wayne K.A., and Gaifa L. Synthesis (1995) 1287-1290
26. Lars G.B., and John R.S. J. Org. Chem. 58 (1993) 5095-5100